35,966 Clinical Contract jobs in the United States

Job Title: Clinical Research Nurse

Job Description

Join a dynamic team focused on either Breast or Phase 1 solid tumor research at their main campus. Collaborate closely with a team of two other nurses and two coordinators, providing essential support in clinical settings.

Responsibilities

• Collaborate with coordinators to attend tumor boards and assist in patient identification.

• Aid in the consenting process and development of treatment plans.

• Work with pharmacy teams and providers for protocol approval.

• Conduct follow-up blood draws and PK draws for outpatient pill treatments.

• Coordinate with infusion nurses for follow-up draws in infusion cases.

• Comfortably access and de-access patient ports.

• Possibly perform EKGs, usually done by coordinators.

• Provide training and guidance to the inpatient care team.

• Coordinate with teams for data entry and regulatory tasks.

Essential Skills

• Registered Nurse with a minimum of 2 years of experience.

• Experience in Oncology or Clinical Research.

• Proficiency in clinical care and clinical research.

Additional Skills & Qualifications

• Oncology Clinical Research certification or experience.

Work Environment

The position is based in downtown Detroit. Employees enjoy a flexible start time between 7:00 and 9:00 AM, with schedules adaptable to patient needs. The role offers the opportunity to accrue four weeks of vacation in the first year.

Pay and Benefits

The pay range for this position is $38.00 - $48.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Detroit,MI.

Application Deadline

This position is anticipated to close on Jul 25, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

ClinChoice is searching for a Freelance Clinical Research Nurse to work on a long-term study, at a hospital site in Buffalo, New York. Minimum commitment of 4 hours per month, with additional hours as needed to support patient care (each patient visit will be about 3 hours minimum). The study will last about 1.5 years. The Clinical Research Nurse will play an important role in patient care, regulatory, data collection, and facilitation of meetings to serve as the main point of contact for the overall coordination of the clinical trial. You will be responsible for performing irrigations for patients while they are in the hospital after the surgery. Responsibilities will include training patients to correctly use an irrigation medical device. No clinical trial experience is required. This position requires 1099 status and self-employment. The schedule is flexible, with work hours provided well in advance with an average of 4-8 hours/month.

ClinChoice is a global full-service CRO with a strong focus on quality, professional development and supportive culture. As a client-facing role, we are looking for a confident candidate with the ability to work independently whilst establishing a high-trust environment with the client counterparts.

Main Job Tasks and Responsibilities:

• Direct the activities of professionals engaged in clinical research projects to ensure compliance with protocols and overall clinical objectives.
• Ensure compliance with each study's protocol by providing thorough review and documentation at each subject study visit.
• Administer investigational products and performs patient assessments during clinical visits to determine the presence of side effects; notifies Principal Investigator of findings/issues.
• Provides patient education and medical information to study patients to ensure understanding of proper investigational produce use, administration, and disease treatment.
• Documents medical data in the patient charts to capture protocol requirements.
• Schedule site visits.
• Monitors study activities to ensure compliance with protocols and with relevant local, federal and state regulatory and institutional policies. Maintains required records of patient performance and ability to use device.
• Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies. Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Identifies protocol problems, informs investigators of problems, or assists in problem resolution efforts such as protocol revisions.
• Patient care / visit will be 3 hours minimum.

• Minimum of a diploma from an accredited nursing school required; Bachelor of Nursing or a Licensed nurse.
• Two years of recent clinical nursing experience in a hospital, clinic, or similar health care setting. Bachelor's degree may be substituted for one year of work experience.
• Nursing competency skills per scope of practice, including performing vital signs, nursing assessments, performing ECG/EKG, administering injections, etc.
• Experience in critical care and post-operative care is preferred.
• At least one year of clinical trials research experience is preferred.
• Medical Device study experience (beneficial).
• Experience using Electronic Data Capture (EDC) systems.
• Experience facilitating IRB submissions.
• Experience with site budget review.
• Training will be provided.
• Knowledge of biological and medical terminology.
• Understanding of the principles of administration and management.
• Detail-orientated and meticulous in all aspects of work.
• Strong attention to detail, proactively identifying and solving problems; ability to demonstrate initiative.
• Proficiency in Microsoft Office (e.g., Word, Excel, Outlook).
• Must be able to lift 15 pounds at a time.

Job Title: Student

Location: East Brunswick (EB)

Department Name: Clinical Research

Req #: 000206366

Status: Hourly

Shift: Day

Pay Range: $0.83 - 20.83 per hour

Pay Transparency:

The above reflects the anticipated hourly wage range for this position if hired to work in New Jersey.

The compensation offered to the candidate selected for the position will depend on several factors, including the candidate's educational background, skills and professional experience.

Summary

The Childrens Specialized Hospitals Research Internship Program hosts cohorts of undergraduate and graduate students during the Fall, Spring and Summer semesters,

During the internship students

Learn how to analyze research articles and summarize key literature by participating in our Bi Monthly Journal Club,

Establish an understanding of CSHs 5 core areas by engaging in program specific projects,

Based on skillsets and research needs, each intern is paired with an active project or research team that working within our five research areas Autism, Brain Injury, Chronic Health Conditions, Cognition, and Mobility,

Interact with CSH clinical staff and scientific collaborators by conducting clinician interviews, as well as attending local events or clinical team meetings taking place across the RWJBarnabas Health campus,

Responsibilities, duties, and projects

16 hours per week minimum requirement including at least 8 hours on site for 12 weeks

Participation in biweekly journal club

Attendance at weekly meetings with the internship cohort

A staff interview and presentation

A final project, which will be presented during the final weeks of the internship

Completion of work specified by assigned team, may include, data management, data entry, data analysis, literature review, participant recruitment, research engagement activities,

Team specific responsibilities below

Chronic Illness Management Program team

Manage program database in REDCap, including reviewing patient medical records and inputting data

Attend Chronic Illness Management clinic appointments and take notes as applicable

Conduct literature reviews

Other responsibilities not otherwise specified to support program needs

RWJBarnabas Health is an Equal Opportunity Employer

Job Title: Clinical Research Nurse

Job Description

We are seeking a dedicated Clinical Research Nurse to join our team. In this role, you will be responsible for recruiting, screening, and enrolling subjects into clinical trials. You will explain the informed consent process to participants and document any adverse events. Additionally, you will collect study documents, protocols, regulatory documents, informed consents, case report forms, and source documents. The preparation of Institutional Review Board (IRB) applications will also be part of your duties.

Responsibilities

• Recruit, screen, and enroll subjects into clinical trials.

• Explain the informed consent process to participants.

• Document adverse events during the trials.

• Collect study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.

• Prepare Institutional Review Board (IRB) applications.

Essential Skills

• Experience with patient enrollment and consenting.

• Knowledge of informed consent processes.

• Experience in oncology clinical trials.

• Proficiency with GCP, EDC, and clinical research coordination.

• Chart review expertise.

• 2+ years of clinical research experience.

• Experience with adverse event reporting.

• Effective communication and writing skills.

• Knowledge of IRB and human research protection regulations.

Additional Skills & Qualifications

• BA/BS degree preferred.

• Experience with in-hospital clinical research.

• Oncology experience required

Work Environment

This position offers a combination of an office and hospital/outpatient surgery setting. The work environment is fast-paced with a high volume workload involving industry and investigator studies. You will be part of one of the most prestigious academic research institutes in the world, equipped with state-of-the-art technology. The role involves working on high-profile studies with large, well-known sponsors.

Pay and Benefits

The pay range for this position is $40.00 - $45.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Philadelphia,PA.

Application Deadline

This position is anticipated to close on Jul 31, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email (% ) for other accommodation options.

As a Research Nurse Coordinator , you'll play a key role in the coordination and execution of clinical research studies. You will be the vital link between research participants, principal investigators, study sponsors, and our interdisciplinary care teams. This role offers a unique opportunity to combine your clinical expertise with research coordination, supporting innovative studies that may impact patient outcomes and the future of medicine.

Key Responsibilities:

• Coordinate clinical study activities to ensure protocol adherence, regulatory compliance, and participant safety.
• Act as a liaison between study participants, investigators, and research staff.
• Educate patients and families on study protocols, clinical conditions, and disease processes.
• Schedule and manage research participant visits and follow-ups.
• Monitor and document adverse events and ensure proper reporting.
• Collaborate with clinical teams to safely and effectively collect and document research data.
• Present study information to interdisciplinary teams and ensure alignment with research goals.
• Triage participant concerns by phone, providing appropriate clinical support.

Qualifications:

• Associate Degree or Nursing Diploma required (BSN preferred).
• Active RN license in the State of California.

Experience:

• Research Nurse Coordinator I : 1-2 years of clinical nursing experience, with at least 1 year in a research setting (e.g., coordinating trials, working with protocols, engaging with IRBs, etc.).

• Research Nurse Coordinator II : 2-3 years of clinical nursing experience, with at least 2 years in research setting , ideally within an academic medical center or industry-sponsored trial environment.

Experience may include:

• Informed consent processes
• Protocol development and study start-up
• Clinical trial data entry and quality assurance
• Regulatory submissions and sponsor interactions
• Monitoring and documentation of patient safety and compliance

• Provides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc.
• Reviews and executes clinical research protocols.
• Completes and maintains study documents in accordance with sponsor and site requirements.
• Possible recruitment of potential study subjects.
• Screens subjects for eligibility, and schedules subjects for study specific assessments, as designated on the Delegation of Authority Log.
• Completes and maintains Case Report Forms in agreement with the source documentation and in accordance with study protocol.
• Accompanies sponsor representatives during their visits and maintains effective and ongoing communication with the sponsor.
• Maintains adequate inventory of all data and supplies.
• Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned.
• Observes, documents, reports, and follows up on adverse events and serious adverse events.
• Conducts the informed consent process, per CenExel Standard Operating Procedures.
• Follows up appropriately on all laboratory results.
• Maintains safety standards when performing job responsibilities.
• Maintains study logs and site relations
• Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens.
• Is on call to answer questions for other members of support staff, study patients or other medical staff, as necessary.
• Assists with quality assurance activities and completes queries, as applicable.
• Obtains Principal Investigator signatures on necessary documents.
• Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol.
• Ensures accountability and adequate supply for study and clinical drugs.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

• Must be a Registered Nurse with a current license in the state in which the employee will be working.
• Must be capable of performing all clinical tasks relevant to licensure and/or training.
• Must have experience placing IV
• Must be able to clearly communicate verbally with patients in both English and Spanish.
• Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc.
• Must be self-motivated and able to perform tasks independently.
• Ability to react calmly and effectively in emergency situations.
• Must reflect the professional image of the company, upholding the company vision in actions and demeanor.

1. Indoor, Office environment.
2. Essential physical requirements include sitting, typing, standing, and walking.
3. Lightly active position, occasional lifting of up to 20 pounds.
4. Reporting to work, as scheduled, is essential.

• Conduct comprehensive nursing assessments, perform clinical procedures (e.g., blood draws, EKGs), and document patient data accurately.
• Coordinate recruitment, screening, and enrollment of research participants, ensuring eligibility and informed consent.
• Schedule and conduct study visits, collect and enter data, and manage subject registration in OnCore.
• Maintain regulatory compliance by preparing and submitting IRB documentation, managing regulatory binders, and attending sponsor visits.
• Perform Epic research billing reviews and triage patient communications related to clinical status, medications, and study participation.

• Must be a licensed Registered Nurse (RN).
• Certified Clinical Research Nurse (CRN) with hands-on clinical research experience.
• Strong knowledge of regulatory requirements and compliance in clinical trials.
• Proven experience working on industry-sponsored clinical trials.
• Skilled in patient care, including assessments, procedures, and communication.
• Proficient in using clinical and research systems such as Epic and OnCore.
• Experience with IRB submissions and maintaining regulatory documentation.
• Excellent organizational, communication, and data management skills.

Northern Light Eastern Maine Medical Center

Department: Cancer Research

Position is located: Lafayette Building, Brewer, ME

Work Type: Full Time

Hours Per Week: 36 Hour/Week

Work Schedule: 7:30 AM to 5:00 PM

Eligible for Sign on Bonus

Summary:

The Cancer Research Nurse is responsible for the day-to-day management of research trials through close out.

Responsibilities:

Participates in the informed consent process of study subjects at all NL EMMC participating sites to include screening all new patients daily -determines preliminary eligibility- informs physician- follows through with patients for possible entry into clinical trial.

Supports the safety of clinical research patients/research participants

Coordinates protocol related research procedures, study visits, and follow-up care with all participating sites

Screens, recruits and enrolls research participants

Maintains study source documents

Reports adverse events

Understands and is compliant with good clinical practice (GCP) and regulatory compliance with CITI training completion

Educates staff at remote NL EMMC participating sites on protocol, study intervention, study drug, etc.

Educates subjects and family on protocol, study intervention, study drug, etc.

Complies with Institutional policies, standard operating procedures (SOPs) and guidelines

Works closely with clinical trials team to identify, implement and successfully conduct cooperative group, industry, and investigator-led clinical trials.

Ensures financial, operational, accrual and other strategic targets are met. Develops and implements corrective action plans as necessary to improve productivity, quality and/or process workflows.

Works closely with physicians and study teams at all participating sites to ensure efficient and timely implementation of new genomic trials and ensures and maintains ongoing compliance with company policies and procedures, SOPs, ICH/GCP guidelines, and FDA regulations.

Brings oncology research subject matter expertise to the planning and execution of study start-up processes, to include remote NL EMMC participating sites, including:

-- study feasibility,

-- Medicare Coverage Analysis development (SOC vs NSOC assessments) and study budget negotiations

-- Study startup operational efficiency and effectiveness

Participates in the development of policies and procedures, and other tools to support the studies with the research manager

May represent the interests of the oncology research program at local/national meetings and educational conferences pertinent to public relations and future business development.

Other Information:

• BLS Required.

• Exceptional organizational and clinical research management skills

• Excellent interpersonal skills with the ability to build strong relationships across multiple organizations

• Excellent time management, critical thinking, analytical and problem-solving skills

• Advanced computer skills, including CTMS, EDC, document management systems, databases and Microsoft Office suite

Competencies and Skills

• Behaves with Integrity and Builds Trust: Acts consistently in line with the core values, commitments and rules of conduct. Leads by example and tells the truth. Does what they say they will, when and how they say they will, or communicates an alternate plan.

• Cultivates Respect: Treats others fairly, embraces and values differences, and contributes to a culture of diversity, inclusion, empowerment and cooperation.

• Fosters Accountability: Creates and participates in a work environment where people hold themselves and others accountable for processes, results and behaviors. Takes appropriate ownership not only of successes but also mistakes and works to correct them in a timely manner. Demonstrates understanding that we all work as a team and the quality and timeliness of work impacts everyone involved.

• Practices Compassion: Exhibits genuine care for people and is available and ready to help; displays a deep awareness of and strong willingness to relieve the suffering of others.

Credentials

• Required Registered - with current OCN or CRA/CRC certification preferred (ACRP or SoCRA)

3+ years of oncology research experience

Education

• BS degree in life sciences or related research field required (advanced degrees preferred)

Working Conditions

• Need to drive to perform responsible duties.

• Work with computers, typing, reading or writing.

• Prolonged periods of sitting.

Position Clinical Research NurseLocation Req ID null

• 42,000+ babies born and counting
• 25,000+ IVF procedures - the most in the Midwest
• 11 nationally recognized physicians leading the charge
• Holistic and mental health integration long before it was mainstream
• State-of-the-art facilities that blend science and compassion

• Coordinate and maintain regulatory documents for active clinical trials
• Collaborate with investigators, coordinators, and sponsors to drive study success
• Educate and support patients throughout their participation in fertility studies
• Track protocols, obtain informed consent, and maintain accurate study documentation
• Assist with procedures, consultations, and routine assessments as needed
• Train and support clinical staff on research protocols and documentation
• Deliver direct patient care including medication administration and vital signs

• Current Illinois RN license
• 3+ years of clinical research experience (IRB/GCP/FDA compliance required)
• Experience with FDA-regulated trials and patient-facing clinical work
• Strong organizational and interpersonal skills - you love a good checklist and a great conversation
• Ability to work independently and collaboratively across disciplines
• Current CPR certification (or ability to obtain within 30 days)

• A mission that matters - be part of making dreams come true
• Blue Cross/Blue Shield Medical , dental, vision, life, LTD/STD & 401(k)
• Generous PTO + 7 paid holidays
• Tuition reimbursement up to $4,500/year
• Pre-tax commuter benefits and Flexible Spending Accounts