96,896 Clinical Contract jobs in the United States

At Houston Methodist, the Clinical Research Fellow position is responsible for performing clinical research of a complex nature; plans, executes and completes clinical research projects under the supervision/direction of a Principal Investigator. This position provides structured education and first-hand applied experiences in such topics as epidemiology, biostatistics, clinical pharmacology, and biomedical ethics/regulation and a certificate of fellowship is granted to the Clinical Research Fellow upon satisfactory completion of the fellowship program.
**PEOPLE ESSENTIAL FUNCTIONS**
+ Directs patient contact supporting the performance of clinical protocols.
+ Enrolls subjects into prospective studies and obtains informed consent from patients and legally authorized representatives in accordance with hospital policy and the study protocol.
+ Collaborates with the Principal Investigator, interprofessional research team, fellowship stakeholders, and health care professionals regularly for problem resolution and/or achievement of research study goals.
+ Serves as a mentor and provides educational and research oversight for other learners in the applicable department or research lab. Role models effective verbal, non-verbal and written communication, which includes active listening and teaching, assisting in development of such skills. Provides contributions towards improvement of department scores for employee engagement, i.e., peer-to-peer accountability.
**SERVICE ESSENTIAL FUNCTIONS**
+ Collects and processes study data and maintain study databases in accordance with study protocols.
+ Develops and conducts statistical analyses for interventional and observational studies using relevant statistical software.
**QUALITY/SAFETY ESSENTIAL FUNCTIONS**
+ Participates in study data auditing and monitoring procedures.
+ Ensures study procedures are being conducted in accordance with hospital and research institute policy and Good Clinical Practice.
+ Communicates study findings to applicable hospital committees and stakeholders.
+ Completes fellowship objectives and all assigned duties as listed in the identified specific fellowship program.
**FINANCE ESSENTIAL FUNCTIONS**
+ Participates in grant preparation and formal requests to solicit financial support for ongoing and planned studies.
+ Manages study finances and resources needed to conduct a clinical study. Self-motivated to independently manage time effectively and prioritize daily tasks.
**GROWTH/INNOVATION ESSENTIAL FUNCTIONS**
+ Develops study protocols, policies, procedures, and order sets based on evidence from published studies and findings from internal studies.
+ Prepares and delivers educational presentations and deliver written reports of scholarship, including but not limited to, published manuscripts in peer-reviewed journals, quarterly activity reports to fellowship stakeholders, and activity reports to external study sponsors as needed.
+ Assists with recruitment of future fellows into this fellowship training program.
This job description is not intended to be all-inclusive; the employee will also perform other reasonably related business/job duties as assigned. Houston Methodist reserves the right to revise job duties and responsibilities as the need arises.
**EDUCATION**
+ Doctor of Medicine (MD) from an accredited medical school, Pharm D or Doctoral degree (PhD) in medical field
**WORK EXPERIENCE**
+ Clinical Research Fellow 0 - NoneClinical Research Fellow 1 - One year of post-terminal experienceClinical Research Fellow 2 - Two years of post-terminal experienceClinical Research Fellow 3 - Three years of post-terminal experienceClinical Research Fellow 4 - Four years of post-terminal experience
**LICENSES AND CERTIFICATIONS - REQUIRED**
+ N/A
**KNOWLEDGE, SKILLS, AND ABILITIES**
+ Demonstrates the skills and competencies necessary to safely perform the assigned job, determined through on-going skills, competency assessments, and performance evaluations
+ Sufficient proficiency in speaking, reading, and writing the English language necessary to perform the essential functions of this job, especially with regard to activities impacting patient or employee safety or security
+ Ability to effectively communicate with patients, physicians, family members and co-workers in a manner consistent with a customer service focus and application of positive language principles
+ Ability to work effectively in a fast-paced environment
+ Demonstrates flexibility and adaptability in the workplace
**SUPPLEMENTAL REQUIREMENTS**
**WORK ATTIRE**
+ Uniform No
+ Scrubs Yes
+ Business professional No
+ Other (department approved) Yes
**ON-CALL***
_*Note that employees may be required to be on-call during emergencies (ie. DIsaster, Severe Weather Events, etc) regardless of selection below._
+ On Call* No
**TRAVEL***
_**Travel specifications may vary by department**_
+ May require travel within the Houston Metropolitan area No
+ May require travel outside Houston Metropolitan area No
**Company Profile:**
Houston Methodist Academic Institute oversees the Education Institute and Research Institute, including 772 faculty and 56,250 learners. The Academic Institute aligns our research and education initiatives in service to the clinical mission, providing solutions that answer the call for new technologies and skills our clinicians need for patient care.
Houston Methodist Education Institute coordinates our primary academic affiliation with Weill Cornell Medicine and other joint programs, including the Engineering Medicine Program at Texas A&M University Intercollegiate School of Engineering Medicine. The Education Institute also oversees continuing medical education and graduate medical education, and supports more than 1,000 trainees in residence for medical, nursing, allied health and research education programs.
Houston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval. The Research Institute supports more than 1,387 clinical research protocols and $70.3 million in extramurally funded translational research programs.
Houston Methodist is an Equal Opportunity Employer.

**Job Type:** Regular
**Time Type:** Full time
**Work Shift:** Day (United States of America)
**FLSA Status:** Non-Exempt
**When you join the growing BILH team, you're not just taking a job, you're making a difference in people's lives.**
Under minimal supervision and direction will be responsible for the coordination and administration of multiple research studies. Responsible for assigned research studies and general research duties. Implements study protocols in accordance to regulatory and institutional requirements. Works closely with principal investigators, research staff and Research Administration facilitating all aspects of assigned clinical trials. Interacts with study participants diagnosed with various medical conditions and diagnoses.
**Job Description:**
1) Possesses ongoing knowledge of FDA, OHRP and GCP regulations:
+ Ensures adherence to regulations.
+ Educates and mentors other study staff as applicable.
2) Responsible for coordinating different phases of research studies with varying degrees of complexity with minimal oversight:
+ Completes and submits trial feasibility forms; coordinates and obtains non-disclosure agreements.
+ Arranges and conducts pre-study qualification and site visits.
+ Acts as the main liaison of communication between sponsors and investigators in all aspects of study start up.
3) Implements assigned research studies by reviewing study and assessing protocol and institutional requirements:
+ Implements all study protocols in accordance with research SOPs, FDA, OHRP, and GCP regulations.
+ Immediately develops coordinator/sponsor relationship.
+ Completes start- up checklists and organizes study start-up plan, including source worksheet creation.
+ Prepares, completes and submits regulatory documents in a timely manner.
+ Prepares, completes and submits start up IRB documents in a timely manner.
+ Reviews all pertinent study documents for potential implementation issues and implements plan accordingly.
+ Ensures appropriate training and certification for all members of the study team involved in the research protocol.
+ Establishes and communicates study procedures with collaborating departments to ensure compliance with all study requirements; conducts in-services (e.g. arranges special blood draws with phlebotomy, special blood processing with specimen processing, ordering and receiving of drug with the pharmacy and infusion team, and copying and submission of MRI with Radiology).
+ Works collaboratively with research finance to process clinical trial agreements, study budget development and other finance issues, as applicable.
+ Attends Investigator Meetings as applicable.
4) Conducts assigned research studies per protocol requirements, departmental and institutional policy:
+ Creates and maintains eRegulatory, patient study and CRF files.
+ Thoroughly learns assigned protocols and serves as resource for all study team members.
+ Responsible for ensuring protocol adherence by understanding, communicating and making sure the study parameters are ordered and carried out per protocol requirements.
+ Advises physicians on required tests, timing of tests and procedures.
+ Ensures that all appropriate treating physicians receive the results of study tests, as appropriate.
+ Administers questionnaires and assessments as mandated by the protocol and delegated by the PI.
+ Directly retrieves and/or coordinates the retrieval and submission of patient samples or tests (e.g., blood samples, urine samples, tissue, ECG, etc.).
+ Submits all IRB submission documents such as protocol amendments and consent form revisions, annual reviews, adverse events, investigator changes, accrual status change and change in risk to the IRB in a timely manner with minimal assistance/guidance from senior staff; Complies with IRB decisions, conditions and requirements.
+ Utilizes current systems to schedule tests and appointments and to access patient data and test results.
+ Establishes monitoring tools to ensure the adherence to study guidelines (e.g. patient enrollment tracking).
+ May assist with the coordination of preparing summary reports, study results, poster presentations and manuscripts for publication.
5) Recruits patients to assigned research studies:
+ Works closely with physicians to develop recruitment strategies.
+ Creates research brochures and other related recruitment materials; creates and/or reviews study trial listing for the Lahey website.
+ Actively screens for and identifies eligible patients through various means (e.g. physician schedules, clinical or research databases, website response).
+ Evaluates patient data to determine if patient meets study eligibility, including reviewing screening eligibility tests, under minimal supervision.
+ Contacts and screens potential subjects for the study.
+ Participates in the informed consent process; obtains subjects signatures and processes appropriately per research policies.
+ Registers or randomizes study participants to assigned research study and treatment/arm; schedules and attends study follow-up visits, as applicable.
6) Performs Data Management duties:
+ Prepares for each study participant visit to ensure all appropriate study procedures are done per protocol; ensures patient visit/test is billed correctly to either insurance or the research account per schema.
+ Completes source worksheets and case report forms (CRFs) as dictated by the assigned research study (i.e. required forms in the required format in the required time interval); Ensures CRF's and source are complete and done correctly.
+ Provides source documentation from the medical chart for all information that is recorded.
+ Submits CRFs to the sponsor as dictated by the study; Maintains sufficient files in the department to document submission and maintain source documentation.
+ Ensures proper placement of consent and related study materials in EMR system.
+ Maintains study supplies and reorders as necessary.
7) Maintains a professional relationship with sponsors and/or CRO's and related members:
+ Maintains regular and appropriate communication.
+ Works with sponsor monitors during monitoring visits; promptly responds to sponsor requests for additional material, clarifying material or missing material.
+ Works cooperatively with sponsor to ensure that good clinical practice are being followed.
+ Resolves data queries timely and appropriately.
+ Schedules sponsor audits, as requested, and is available during audit to review CRFs and procedures with sponsor personnel, as necessary.
+ Completes study close out activities at the end of the study.
+ Retains records and archives documents according to institutional SOPs.
8) Works in collaboration with research finance on all study related finances including clinical trial agreements, budget preparation, patient related study visits, invoicing and helping to resolve study subject billing issues.
9) Seeks additional training or guidance when necessitated; utilizes available research tools and resources.
10) Completes and maintains all required trainings:
+ Participates in and actively seeks continuing education opportunities.
+ Maintains required continuing education credits per institutional and departmental SOPs.
11) Participates and assists in other research projects and initiatives as assigned:
+ Is a team player within the department.
+ Is flexible with time when applicable.
**Organizational Requirements:**
Maintain strict adherence to the Lahey Hospital and Medical Center Confidentiality policy.
Incorporate Lahey Hospital and Medical Center Standards of Behavior and Guiding Principles into daily activities.
Comply with all Lahey Hospital and Medical Center Policies.
Comply with behavioral expectations of the department and Lahey Hospital and Medical Center.
Maintain courteous and effective interactions with colleagues and patients.
Demonstrate an understanding of the job description, performance expectations, and competency assessment.
Demonstrate a commitment toward meeting and exceeding the needs of our customers and consistently adheres to Customer Service standards.
Participate in departmental and/or interdepartmental quality improvement activities.
Participate in and successfully completes Mandatory Education.
Perform all other duties as needed or directed to meet the needs of the department.
**Minimum Qualifications:**
Education:
Bachelor's degree required
In absence of a Bachelor's degree, will consider 8 years of relevant work experience in addition to the experience noted below.
Licensure, Certification & Registration:
None required
Experience:
2-5+ years direct work related experience in a research setting
Skills, Knowledge & Abilities:
Ability to demonstrate basic knowledge of fundamental concepts, practices and procedures with the ability to use them in varied situations; Ability to make decisions that are guided by general instructions and practices requiring some interpretation; Seeks assistance when confronted with difficult and/or unpredictable situations; Ability to travel nationally to other research sites, attend investigator meetings and educational conferences as required; Strong verbal and written communication, multi-tasking, attention to detail and organizational skills; Ability to interact with professional personnel at all levels; ability to communicate clearly and effectively; Ability to demonstrate a positive attitude and respond to requests in a timely and respectful manner; Ability to function independently, set priorities, provide clear direction and training, take initiative and work collaboratively in small teams; Ability to interact with study participant with various diseases compassionately and respectfully; Working knowledge of medical terminology and medical practice protocols; Experience with computer systems, including web based applications; In the absence of any of these skills, demonstrates the ability to be thoroughly trained to meet organizational standards.
**As a health care organization, we have a responsibility to do everything in our power to care for and protect our patients, our colleagues and our communities. Beth Israel Lahey Health requires that all staff be vaccinated against influenza (flu) as a condition of employment.**
**More than 35,000 people working together. Nurses, doctors, technicians, therapists, researchers, teachers and more, making a difference in patients' lives. Your skill and compassion can make us even stronger.**
**Equal Opportunity** **Employer/Veterans/Disabled**

At Stanford University School of Medicine the work we do touches lives today and tomorrow. Through education, research , and healthcare, the School of Medicine improves health through leadership, diversity , collaborative discoveries, and innovation.

Whether working in departments with faculty , or in units that support the school , our staff are a part of teams that propel us on our journey toward the future of medicine and Precision Health.

The department of Pediatrics at Stanford University is seeking a Clinical Research Coordinator Associate (CRC2) to conduct clinical research and work on complex projects / assignments . This interesting and unique opportunity will oversee the clinical research functions of a multi-site pediatric oncology consortium. Pediatric Oncology Experimental Therapeutics Consortium Research Development and Management Center (POETIC RDMC) is a phase I clinical trial consortium whose mission is "To promote early clinical development of promising therapies for children, adolescents , and young adults with cancer and related disorders". This position will oversee significant and key aspects of the consortium large research studies and work under close direction of the principal investigator and / or study supervisor.

Duties include:

• Serve as primary contact with research participants, sponsors , and regulatory agencies. Coordinate studies from startup through close-out.

• Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.

• Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents / case report forms.

• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed.

• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents , and attend monitoring meetings with sponsors , acting as primary contact.

• Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and / or management staff.

• Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.

• Participate in monitor visits and regulatory audits.

* - Other duties may also be assigned

All members of the Department of Pediatrics are engaged in continuous learning and improvement to foster a culture where diversity, equity, inclusion, and justice are central to all aspects of our work. The Department collectively and publicly commits to continuously promoting anti-racism and equity through its policies, programs, and practices at all levels.

Stanford University provides pay ranges representing its good faith estimate of what the University reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs. The pay range for this position working in the California Bay area is $84,856.00 to 97,021.00 annually

DESIRED QUALIFICATIONS:

• Bachelor's degree in related medical field.

• Experience working with oncology clinical research studies.

• 1-2 years of experience in a clinical research setting is highly desirable .

EDUCATION & EXPERIENCE (REQUIRED):

Two-year college degree and two years related work experience or a Bachelor's degree in a related field or an equivalent combination of related education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Strong interpersonal skills.

• Proficiency with Microsoft Office.

• Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

PHYSICAL REQUIREMENTS*:

• Frequently stand , walk, twist, bend, stoop, squat and use fine light / fine grasping.

• Occasionally sit , reach above shoulders, perform desk based computer tasks , use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.

• Rarely kneel, crawl, climb ladders, grasp forcefully , sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

* - Consistent with its obligations under the law , the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

Location Detail: 560 Hudson St HH E&R Ctr (10058)

Shift Detail: Monday-Friday

Work where every moment  matters.

Every day, almost 30,000 Hartford HealthCare employees come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.

Responsibilities:
• Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
• Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
• Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
• Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
• Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
• Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
• Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
• Assist/coordinate preparation for internal and external audits.
• Handle all confidential information appropriately.

Qualifications

Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
• Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) and querying.
• Experience with Microsoft Access, Excel and electronic data capture systems.
• Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant documentation protocols.
• Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team.
• Ability to travel between clinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment .

Location Detail: 560 Hudson St HH E&R Ctr (10058)

Shift Detail: Monday-Friday

Work where every moment  matters.

Every day, almost 30,000 Hartford HealthCare employees come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.

Responsibilities:
• Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
• Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
• Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
• Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
• Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
• Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
• Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
• Assist/coordinate preparation for internal and external audits.
• Handle all confidential information appropriately.

Qualifications

Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
• Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) and querying.
• Experience with Microsoft Access, Excel and electronic data capture systems.
• Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant documentation protocols.
• Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team.
• Ability to travel between clinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment .

Location Detail: 560 Hudson St HH E&R Ctr (10058)

Shift Detail: Monday-Friday

Work where every moment  matters.

Every day, almost 30,000 Hartford HealthCare employees come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.

Responsibilities:
• Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
• Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
• Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
• Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
• Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
• Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
• Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
• Assist/coordinate preparation for internal and external audits.
• Handle all confidential information appropriately.

Qualifications

Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
• Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) and querying.
• Experience with Microsoft Access, Excel and electronic data capture systems.
• Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant documentation protocols.
• Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team.
• Ability to travel between clinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment .

Location Detail: 560 Hudson St HH E&R Ctr (10058)

Shift Detail: Monday-Friday

Work where every moment  matters.

Every day, almost 30,000 Hartford HealthCare employees come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.

Responsibilities:
• Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
• Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
• Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
• Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
• Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
• Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
• Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
• Assist/coordinate preparation for internal and external audits.
• Handle all confidential information appropriately.

Qualifications

Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
• Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) and querying.
• Experience with Microsoft Access, Excel and electronic data capture systems.
• Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant documentation protocols.
• Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team.
• Ability to travel between clinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment .

Location Detail: 560 Hudson St HH E&R Ctr (10058)

Shift Detail: Monday-Friday

Work where every moment  matters.

Every day, almost 30,000 Hartford HealthCare employees come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.

Responsibilities:
• Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
• Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
• Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
• Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
• Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
• Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
• Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
• Assist/coordinate preparation for internal and external audits.
• Handle all confidential information appropriately.

Qualifications

Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
• Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) and querying.
• Experience with Microsoft Access, Excel and electronic data capture systems.
• Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant documentation protocols.
• Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team.
• Ability to travel between clinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment .

Location Detail: 560 Hudson St HH E&R Ctr (10058)

Shift Detail: Monday-Friday

Work where every moment  matters.

Every day, almost 30,000 Hartford HealthCare employees come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.

Responsibilities:
• Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
• Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
• Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
• Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
• Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
• Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
• Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
• Assist/coordinate preparation for internal and external audits.
• Handle all confidential information appropriately.

Qualifications

Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
• Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) and querying.
• Experience with Microsoft Access, Excel and electronic data capture systems.
• Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant documentation protocols.
• Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team.
• Ability to travel between clinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment .