2,767 Clinical Research Associates jobs in the United States
Clinical Research Coordinator/Clinical Research Coordinator, Licensed
Posted 2 days ago
Job Viewed
Job Description
Virginia Commonwealth University (VCU) School of Medicine is a premier academic medical center located in the heart of Richmond. Accounting for almost half of VCU's sponsored research, the School of Medicine is internationally recognized for patient care and education. All full-time university staff are eligible for our generous benefits package that includes choices for health, vision, and dental coverage, life-insurance, short and long-term disability coverage, retirement planning, tax-deferred annuity and cash match programs, flexible spending accounts, tuition benefits, significant paid-time off, 12 paid holidays, and more. Explore our benefits further here:
Summary :
Position Summary: Coordinate various clinical research programs dealing with diagnostic and therapeutic aspects of chronic liver disease and its complications under the direction of physicians within the Hepatology Section. Ensure patient safety is a top priority in conducting clinical trials. Ensure all IRB submissions are complete and submitted on time. Maintain regulatory binders in audit ready state- ensuring all documentation is complete and has been submitted to the IRB. Provide timely and courteous responses to queries from patients, faculty and sponsors. Complete and ensure accurate effort reporting is recorded.
Key Responsibilities include :
- Patient Evaluation
o Evaluate patients for eligibility to participate in various programs to treat chronic liver disease. o Review medical records pertaining to these patients.
o Present this data to the attending physician group for review.
- Patient Education
o Educate patients concerning natural history of chronic liver disease and its complications. o Educate patients concerning the side effects of specific medications and other treatment of chronic liver disease
- Coordination of Patient Care
o Work with research nurse coordinators at other sites involved in multi-center clinical trials, the Project Manager at the VCU site, and NIH personnel to coordinate care of patients and to ensure consistency in treatment.
-Patient Phone Support
Answer phone questions for patients concerning possible side effects of the treatments they are receiving as well as complications associated with chronic liver disease or any other acute illness. o Assess this information and present to attending physicians within the Hepatology Section as appropriate
-Data Analysis and Presentation
o Complete study collection forms necessary to evaluate effects of treatment of chronic liver disease.
o Analyze data with use of the personal computer and produce graphic illustrations of this data. Present this information to the attending physicians of the Hepatology Group
-Risk Management
o Demonstrates a commitment to risk assessment (considering cost, benefit, and impact) o Utilizes identified internal control mechanism. Practices routine verification of the accuracy of data
Minimum Hiring Standard s:
-RN Licensure Required
-Experience with direct patient care
-Desire to work independently and closely with patients and physicians Good communication skills
-Demonstrated experience working in and fostering a diverse faculty, staff, and student environment or commitment to do so as a staff member at VCU
Preferred Qualifications:
-Familiarity with Epic
-Familiarity with VCUHS
Position is Open Until Filled
This is a restricted position with no set end date; continued employment is dependent upon project need, availability of funding, and performance.
ORP Eligible: No
Virginia Commonwealth University is an equal opportunity, affirmative action university providing access to education and employment without regard to race, color, religion, national origin, age, sex, political affiliation, veteran status, genetic information, sexual orientation, gender identity, gender expression, or disability.
Please note that if you are employed as a university employee working in any of the health system's facilities, you will need to follow VCU Health System policies, which will include but will not be limited to, vaccination requirements.
The School of Medicine continuously strives for our workplace and learning environment to reflect the demographic and social milieu of the communities we serve. All qualified applicants are encouraged to apply.
UNIVERSITY JOB CODE: Clinical Research Coordinator 1-3 (34111N-34113N)/Clinical Research Coordinator Licensed 1-3 (34081N-34083N)
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Location:
The Center for Cancer & Blood DisordersPay Range:
$26.73 - $46.99This position supports Center for Cancer and Blood Disorders in Bethesda.
Job Description Summary:
Responsible for the performance of the research study under the medical supervision of the Principal Investigator. Clinical Research Coordinator II (non-RN) performs tasks independently, consistently and accurately, and demonstrate that they have achieved a moderate level of expertise in all of their skills and abilities resulting in high quality work
Primary responsibility includes complex types of study designs (phase 1-3, multi-cohort, interventional trial design) and associated study procedures. Administratively and clinically manage an average 10 clinical trials open to accrual annually and/or active (on study treatment) patient volume over 25 annually
Demonstrates working knowledge of all facets of role, relevant regulations, and organizational and departmental policies and procedures. Performs other duties and projects as assigned. Performs all duties in accordance with regulatory requirements and organizational policies and procedures.
Primary Key Performance Areas
KPA 1 - Protocol Comprehension and Implementation: Coordination of care for patients on clinical research protocols in accordance with GCP, ICH/FDA guidelines and requirements.
- Demonstrate an understanding of protocol elements / requirements and demonstrate the ability to execute study procedures. Demonstrate the ability to anticipate and mitigate the potential for protocol non-compliance.
- Conduct protocol feasibility assessments and complete feasibility/site assessment questionnaires
- Assess subjects on the basis of inclusion/exclusion criteria and demonstrate the ability to evaluate and document subject eligibility independently.
- Reviews draft informed consent documents in compliance with regulatory requirements and GCPs. Conduct an informed consent discussion in compliance with SOPs
- Review and interpret diagnostic test results and related documentation required per protocol
- Follows process for capturing, assessing, determining causal relationship of adverse events to the investigational product, investigator oversight, reporting and following up on adverse events. Recognize, report and follow up on all types of adverse events
- Maintain accurate records of the receipt, inventory, distribution and destruction of study-related materials / investigational products and research specimens.
- Ensure that the investigational drug is received, stored, and documented, and that excess materials are returned to the sponsor according to sponsor guidelines and in accordance with Code of Federal Regulations. Assesses and manages investigational products that have been compromised.
KPA 2 - Regulatory and Data Integrity
- Understanding of the IRB/IEC review, key elements of review considerations, approval and reporting requirements for the site. Complete all IRB/IEC-related documents over the course of a clinical study. Maintains site credentials and ensures updated GCP, licenses remain on file
- Comply with reporting of safety related subject discontinuation and safety concerns (AE, SAE or AE of Interest) to the sponsor and IRB/IEC.
- Autonomously collect, record and report accurate data and demonstrate per FDA guidelines, and review them against the patient's medical record for completeness and accuracy.
- Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
- Manage a monitoring visit including appropriate preparations, support, documentation and follow up. Maintain proper (accurate and timely) communication with the monitor and follow up on all monitor requests
- Implement a CAPA assessment and follow CAPA related issues through to resolution.
- Escalates issues of protocol non-compliance to study PI and research department leadership
KPA 3 - Research Financial Practices: Budget/Contract execution and practices research billing compliance
- Assess a protocol and study plan to develop a study budget.
- Understanding of the payment terms of the study budget and the and tract items that need to be invoiced for a clinical study.
Position Qualifications/Requirements
Education :.
- High school education required
- Some college required, bachelor's degree preferred and/or Licensed Practical Nurse required
Certifications/Licenses : Previous Experience :
- 2-5 years prior oncology research/related medical science experience
Core Capabilities :
- Analysis & Critical Thinking: Critical thinking skills including solid problem solving, analysis, decision-making, planning, time management and organizational skills. Must be detailed oriented with the ability to exercise independent judgment.
- Interpersonal Effectiveness: Developed interpersonal skills, emotional intelligence, diplomacy, tact, conflict management, delegation skills, and diversity awareness. Ability to work effectively with sensitive and confidential material and sometimes emotionally charged matters.
- Communication Skills: Good command of the English language. Second language is an asset but not required. Effective communication skills (oral, written, presentation), is an active listener, and effectively provides balanced feedback.
- Customer Service & Organizational Awareness: Strong customer focus. Ability to build an engaging culture of quality, performance effectiveness and operational excellence through best practices, strong business and political acumen, collaboration and partnerships, as well as a positive employee, physician and community relations.
- Self-Management: Effectively manages own time, conflicting priorities, self, stress, and professional development. Self-motivated and self-starter with ability work independently with limited supervision. Ability to work remotely effectively as required.
- Must be able to work effectively in a fast-paced, multi-site environment with demonstrated ability to juggle competing priorities and demands from a variety of stakeholders and sites.
- Computer Skills:
- Proficiency in MS Office Word, Excel, Power Point, and Outlook required.
- Prior experience with electronic medical records (EMR) is preferred
- Prior experience with clinical trial data entry systems (EDC) preferred
- Prior Clinical Trial Management Systems (CTMS) preferred.
#AONC
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Title: Clinical Research Coordinator Location: Kingwood, TX Type/Duration: Contract, 6 months Schedule: Monday-Friday, core daytime business hours based on clinic hours, could have some earlier morning starts Sta
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Community Focused. Care Driven.
Join Southcoast Health, where your future is as promising as the care we provide. Our commitment to each other, our patients, and our community is more than a mission - it's our way of life, and you'll be at the heart of it.
Southcoast Health is a not-for-profit, charitable, health system with multiple hospitals, clinics and facilities throughout Southeastern Massachusetts and Rhode Island.
Nestled in local communities, Southcoast Health provides inclusive, ethical workplaces where our highly skilled caregivers offer world-class, comprehensive healthcare close to home.
Find out for yourself why Southcoast Health has been voted 'Best Place to Work' for 7 years in a row!
We are searching for a talented Clinical Research Coordinator
A career at Southcoast Health offers you:
- A culture of well-being that embraces, respects, and celebrates the rich diversity of one another and the communities we serve
- Competitive pay and comprehensive benefits package
- Generous Earned Time Off Package**
- Employee Wellbeing Program
- 403B Retirement Plan with company match
- Tuition assistance / Federal Loan Forgiveness programs
- Professional growth opportunities and customized leadership training
**Available to regular status employees who are scheduled to work a minimum of 24 hours.
Southcoast Health is an Equal Opportunity Employer.
Responsibilities Under the direction of the Care Center Director or Designee, perform diversified duties in coordinating all activities related to clinical trials. Duties include but are not limited to oversight of all research-related activities, screening and evaluation of prospective trial patients, clinical follow-up of enrolled trial patients, correspondence and coordination with the Institutional Review Board and trial sponsors. Facilitation and development of relationships with Sponsors for clinical trials. Management/tracking of compliance with Federal and institution guidelines relating to conducting human subject research. Educate patients to clinical trials and obtain informed consent to participate. Responsible for implementing new trials, collaborating with multiple MD Principal Investigators, negotiating and maintaining budgets, managing audits and ensuring adherence to study protocols about mandated visits, medicine management and symptom tracking. Qualifications- Bachelors Degree or the equivalent experience is required. Degree in Healthcare administration, Healthcare, Science or related field is preferred.
- Three to five years of experience working directly in clinical trials involving human subjects is preferred.
- Attention to detail and strong organizational skills are required.
- US Drivers license is required. Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA) is preferred.
- Certification within 6 months of hire. If less than 2 years full time clinical research experience, the minimum allowed before you can sit for the exam, certification will then be required.
-
Must be fully vaccinated against seasonal Influenza and the COVID 19 virus or to be exempt from the requirement for medical or personal reasons by signing a statement certifying you are choosing to be exempt from vaccination once hired.
Compensation: Pay rate will be determined based on level of experience.
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Title: CRC Level I (Clinical Research Coordinator)Location: On-Site (Mt Pleasant/Charleston SC)
Summary: The CRC ensures the safety of our volunteers, promotes the mission of Accellacare, and strives to meet and exceed study priorities. This individual is responsible for recruiting and promoting our service to suitable participants and sponsor representatives. Additionally, the CRC will perform tasks required to coordinate and complete a study according to the protocol.
Duties:
- Performing technical and clinical requirements of study protocols, i.e., venipuncture, specimen processing, vital signs, electrocardiograms, IV infusions, IV pump operations, Holtor monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, injections (IM or SQ) or any procedure necessary for the protocol as ordered by the investigator.
- Attending investigator meetings, site initiation visits, and coordinator meetings to obtain training on drug preparation and administration and general knowledge about a protocol with a focus on clinical procedures.
- Obtaining knowledge about the study drugs with an emphasis on injection or intravenous infusion medications.
- Monitoring for possible complications with the administration of study drugs with an emphasis on injections or intravenous infusions.
- Maintaining accurate dispensing logs, separate from those of the coordinator, to include such information as lot number, drug vs. placebo, and information about the third party mixer or un-blinded mixer/preparer of medication.
- Documenting laboratory data and adverse reactions, and immediately notifying investigators, sponsors and the Institutional Review Board, if indicated, of any unexpected or serious events.
- Assisting other staff members as determined by the needs and priorities of the research organization and as time and abilities permit.
- Actively recruiting and effectively selling our service to suitable patient participants for clinical trials with set time allotted each week for recruitment efforts.
- Proactively promoting the site with monitors and in-house contacts for future trials.
- Responding to queries in a timely manner, prompt data entry and working with the monitor during on-site visits are examples of pro-active behaviors.
- Preparing study documentation in the event of a sponsor or FDA audit and assisting the auditor for the duration of the audit.
- Ordering clinical supplies, as well as ordering, storing and monitoring of protocol specific rescue drugs and maintaining scheduled assessment of the code/crash cart and AED including maintaining proper documentation for both.
- Monitoring and maintaining refrigerators, freezer units and investigational product storage temperatures for safety and stability.
- Obtaining and maintaining knowledge in regards to temperature monitoring devices and procedures for lab specimens and investigational products and providing detailed information to all staff and sponsors in regards to how temperatures are monitored and maintained.
- Maintaining certification for packaging and shipping specimens on dry ice, as well as maintaining and updating knowledge of lab procedures to assist with work flow.
- Acting as the OSHA Representative for the site which would include but not be limited to; maintaining employee immunization records, obtaining vaccines when necessary for site or PMG and administering vaccines to staff.
- Performing equipment calibration when needed, if not performed by the lab coordinator or outside service and maintaining equipment calibration records.
- Supporting training and additional development of clinical skills for site staff as needed
To be successful, you will have:
- Bachelor's life science degree, or relevant industry-field experience
- 1 years' work experience in clinical research or pharmaceutical environment would be desirable
- High level of attention to detail
- Personable, able to build rapport with patients with ease
- Motivated about a career in clinical research
- Excellent planner, organized approach to work
What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family's needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply.
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Center for Clinical Research Management (CCRM) and the Department of Neurology; Neuromuscular Division (ALS Research); assists with assessing patient records to identify patients who are eligible to participate in specified Amyotrophic lateral sclerosis (ALS, Lou Gehrig Disease) clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, amp; other diagnostic testing in accordance with study protocol; participates in the collection, processing amp; evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic and research-related testing and questionnaires; assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, amp; provide appropriate level of care; documents unfavorable responses and notifies research sponsors amp; applicable regulatory agencies; participates in evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data; generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol requirements.
Minimum Education Required
Bachelors Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required. 1 year of relevant experience required.
Minimum Experience Required
1 year of relevant experience required.
Preferred Experience and Qualifications
2-4 years of relevant experience preferred. Experience or knowledge in neuromuscular diseases preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired.
Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.
FUNCTION/SUBFUNCTION: Research and Scholarship/Clinical Research
CAREER BAND: Individual contributor- Specialized
CAREER LEVEL: S2
This position is patient facing and will be required to be onsite.
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Join to apply for the Clinical Research Coordinator role at Providence
3 days ago Be among the first 25 applicants
Join to apply for the Clinical Research Coordinator role at Providence
Get AI-powered advice on this job and more exclusive features.
Description
Independently coordinates research and administrative tasks in support of one or more research studies. Works with study investigators and supervisor to address study-related issues. Backs up other coordinators as needed. Supports department financial performance through budgeting, billing and as directed.
Description
Independently coordinates research and administrative tasks in support of one or more research studies. Works with study investigators and supervisor to address study-related issues. Backs up other coordinators as needed. Supports department financial performance through budgeting, billing and as directed.
May develop specialized research instruments and assist in the preparation of scientific manuscripts or presentations. May entail regular after-hours support, occasional on-call work and occasional overnight business travel.
Exhibits increased productivity and independence relative to Research Coordinator I. Trains other research coordinators in the proper conduct of research studies and participates in quality control activities, as directed.
Providence Swedish caregivers are not simply valued theyre invaluable. Join our team at Swedish Research and thrive in our culture of patient-focused, whole-person care built on understanding, commitment, and mutual respect. Your voice matters here, because we know that to inspire and retain the best people, we must empower them.
Required Qualifications
- Bachelor's Degree Preferably in Science, Healthcare, or other related field Or Significant experience in research coordination may be substituted for educational requirements
- 3 years Experience in related area
- Upon hire: Certified Clinical Research Coordinator (CCRC) or similar professional research certification
Our best-in-class benefits are uniquely designed to support you and your family in staying well, growing professionally, and achieving financial security. We take care of you, so you can focus on delivering our mission of improving the health and wellbeing of each patient we serve.
About Providence
At Providence, our strength lies in Our Promise of Know me, care for me, ease my way. Working at our family of organizations means that regardless of your role, well walk alongside you in your career, supporting you so you can support others. We provide best-in-class benefits and we foster an inclusive workplace where diversity is valued, and everyone is essential, heard and respected. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. As a comprehensive health care organization, we are serving more people, advancing best practices and continuing our more than 100-year tradition of serving the poor and vulnerable.
The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
Providence offers a comprehensive benefits package including a retirement 401(k) Savings Plan with employer matching, health care benefits (medical, dental, vision), life insurance, disability insurance, time off benefits (paid parental leave, vacations, holidays, health issues), voluntary benefits, well-being resources and much more. Learn more at providence.jobs/benefits.
About The Team
Providence Swedish is the largest not-for-profit health care system in the greater Puget Sound area. It is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Whether through physician clinics, education, research and innovation or other outreach, were dedicated to improving the wellbeing of rural and urban communities by expanding access to quality health care for all.
Providence is proud to be an Equal Opportunity Employer. We are committed to the principle that every workforce member has the right to work in surroundings that are free from all forms of unlawful discrimination and harassment on the basis of race, color, gender, disability, veteran, military status, religion, age, creed, national origin, sexual identity or expression, sexual orientation, marital status, genetic information, or any other basis prohibited by local, state, or federal law. We believe diversity makes us stronger, so we are dedicated to shaping an inclusive workforce, learning from each other, and creating equal opportunities for advancement.
Requsition ID: 373891
Company: Swedish Jobs
Job Category: Research
Job Function: Clinical Support
Job Schedule: Full time
Job Shift: Day
Career Track: Clinical Support
Department: 3909 SRE TUMOR INSTIT RESEARCH
Address: WA Seattle 1221 Madison
Work Location: Swedish First Hill 1221 Madison-Seattle
Workplace Type: On-site
Pay Range: $33.05 - $1.30
The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities. Seniority level
- Seniority level Mid-Senior level
- Employment type Full-time
- Job function Research, Analyst, and Information Technology
- Industries Hospitals and Health Care
Referrals increase your chances of interviewing at Providence by 2x
Sign in to set job alerts for Clinical Research Coordinator roles.Greater Seattle Area
25.00
-
34.00
3 weeks ago
Seattle, WA
3,688.00
-
4,145.00
2 weeks ago
Seattle, WA 78,894 - 118,310 2 weeks ago
Redmond, WA 90,000 - 130,000 2 weeks ago
Research Associate II/Senior Research Associate, Analytical Development Clinical Education Specialist - Team Coordinator Sr. Clinical Research Operations SpecialistWere unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-LjbffrBe The First To Know
About the latest Clinical research associates Jobs in United States !
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Job Title: Research CoordinatorJob DescriptionWe are seeking a dedicated Research Coordinator to join our dynamic team in Wilmington, NC. You will play a crucial role in coordinating clinical trials, ensuring compliance with FDA and GCP guidelines, and contributing to the development of new medications. This position offers an opportunity to be part of a best-in-class clinical research site that is committed to changing lives and providing the community with a wide range of trial opportunities.ResponsibilitiesCoordinate clinical trials in accordance with FDA and GCP guidelines.Schedule patient visits and manage trial data using the Electronic Data Capture system, ensuring quality control.Collaborate with the marketing coordinator to recruit subjects for trials.Input visit data into the Clinical Trial Management System (CTMS) to track patient visits and completed procedures.Process lab specimens, label vials, and fill out requisitions accurately for storage or shipment as per study protocol.Prepare and maintain research study files, compiling and submitting study information within established deadlines.Required Skills1+ year of clinical research experience.Pre-screening patients for clinical trials.Expertise in clinical research and patient recruitment.Work EnvironmentJoin our rapidly growing team dedicated to providing the best participant experience during trials. Pay and BenefitsThe pay range for this position is $24.04 - $26.44/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 TypeThis is a fully onsite position in Wilmington,NC.Application DeadlineThis position is anticipated to close on Jul 21, 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.
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Job Title: Clinical Research CoordinatorJob DescriptionThe Clinical Research Coordinator position involves coordinating multiple research protocols and serving as a liaison with local investigators and sponsors. Under direct supervision, the individual will grow in their understanding of research operations and regulations to achieve a fundamental understanding of human subject research.ResponsibilitiesAdhere to the 'Code of Conduct' philosophy and 'Mission and Value Statement'.Complete training assignments promptly as required during employment.Perform routine operational activities for multiple research protocols.Liaise between site research personnel, industry sponsors, and supervisors.Collaborate closely with various site departments/teams, including finance, hospital administrative representatives, and the local IRB.Coordinate schedule of assessments from initial submission of feasibility until study closeout.Review study design and inclusion/exclusion criteria with physicians and patients.Ensure the protection of study patients by verifying informed consent procedures and adhering to protocols.Ensure data integrity by careful source document review and monitor for missing or implausible data.Collect, complete, and enter data into study-specific case report forms or electronic data capture systems.Required Skills & QualificationsBachelor's Degree required.1+ years of relevant clinical research experience required.Pay and BenefitsThe pay range for this position is $28.00 - $35.00/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 TypeThis is a fully onsite position in San Antonio,TX.Application DeadlineThis position is anticipated to close on Jul 11, 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.
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
DescriptionThe research coordinator is primarily responsible for coordinating research patient visits according to both the ICH-GCP guidelines and the IRB-approved study protocol and/or manual of procedures. Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience / knowledge and the needs of the organization which are subject to change from time to time.Duties:•Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study•Administer sponsor required questionnaires (i.e. VFQ)•Works with team member responsible for ordering study supplies (lab kits, shippers, etc.) to ensure adequate inventory is on hand•Ensures study staff is properly trained on study-related information (i.e. protocol, ICF, manuals, etc.) and that the training is documented•Creates, manages, and maintains source documents for each trial•Attends teleconferences and Investigator Meetings as requested by research director•Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections•Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals•Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately•Efficiently completes all study tasks delegated to them (i.e. scribing, VFQ, IOP, etc.)•Collects updated medical history, adverse events and serious adverse events that need to be reported to the sponsor and IRB within required timeframe•Conducts and/or participates in the informed consent process/discussion with research participants, including answering any questions related to the study•Assures that amended consent forms are appropriately implemented and signed•Acts as a secondary reviewer to provide oversight so that the ICF process is conducted accurately•Collects data as required by the protocol and enters information into the electronic data capture (EDC) system in the specified timeframe indicated in the study contract.•Oversees data and ensures that it is being entered correctly and resolves any queries issued within required timeframe•Collects and reports ALL Adverse Events•Collects and reports ALL Serious Adverse Events•Responsible for ensuring all SUSAR/Safety Reports are acknowledged and reviewed•Coordinates monitor site visits and assists with preparation of site visit documentation•Works with the monitor to make any corrections needed to meet requirements and deadlines as needed•Manages and maintains all regulatory information about the study including the protocol, investigator brochure, IRB documents, Investigator disclosures, CVs, training documentation, instructions on reporting requirements for the IRB and the sponsor•Obtain any applicable additional/required sponsor training and/or certifications