clinical research assistant

Cardio Metabolic Institute

Company Overview The Cardio Metabolic Institute is a specialized healthcare facility dedicated to addressing cardiovascular and metabolic health issues. Our multidisciplinary team focuses on advancing research and providing innovative clinical solutions to improve patient outcomes.Job Overview We are seeking a highly motivated Clinical Research Assistant to support our ongoing clinical trials and research projects in cardiovascular and metabolic medicine. The ideal candidate will possess strong laboratory skills, a detail-oriented approach, and a passion for advancing scientific knowledge. This paid position offers an excellent opportunity to contribute to cutting-edge research while gaining valuable experience in clinical research and laboratory techniques.Duties<ul><li>Assist in the preparation and execution of clinical trials, ensuring compliance with FDA regulations and ICH Good Clinical Practice (GCP) standards.</li><li>Maintain accurate documentation review and ensure proper data entry for research records.</li><li>Monitor patients during clinical visits, documenting vital signs and assisting with patient assessments in accordance with HIPAA regulations.</li></ul><ul><li>Qualifications</li><li>Knowledge of clinical trials processes, FDA regulations, and HIPAA compliance is highly desirable.</li><li>Strong organizational skills with meticulous attention to documentation review and data accuracy.</li><li>Ability to work independently as well as collaboratively within a multidisciplinary team environment.</li><li>A degree in biological sciences or related field; relevant certifications such as an ICH GCP certificate are advantageous.</li><li>Join our team to contribute meaningfully to innovative cardiovascular and metabolic research while developing your expertise in clinical science and laboratory techniques!</li><li>Great opportunity for a college graduate in a gap year or someone who wants to build a career in clinical research.</li></ul>Job Type: Full-timePay: $15.00 - $20.00 per hourExpected hours: 30 &ndash; 40 per weekBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Health insurance</li><li>Vision insurance</li></ul>Work Location: In person

Clinical Research Assistant

Spring Clinical Research

Job Description:We are seeking a motivated and detail-oriented Clinical Research Assistant to join our dynamic research team. The successful candidate will play a pivotal role in supporting clinical trials and research studies aimed at advancing medical knowledge and improving patient care. The Clinical Research Assistant will work closely with the research team, study participants, and healthcare professionals to ensure the smooth and ethical execution of research projects.Key Responsibilities:Participant Recruitment and Screening:Identify and recruit eligible study participants according to study criteria. Screen potential participants to ensure their suitability for the research. Data Collection and Documentation:Assist in the collection of clinical data, including medical histories, laboratory results, and vital signs. Maintain accurate and organized records of all research-related activities. Ensure data integrity and compliance with study protocols. Informed Consent Process:Explain the research study to participants and obtain informed consent. Maintain documentation of informed consent processes.Clinical Procedures: Assist with clinical procedures, including administering medications, medical tests, and assessments as per the study protocol. Ensure adherence to ethical and safety standards.Data Management:Enter, manage, and analyze research data using electronic databases and software. Generate reports and assist in data interpretation.Regulatory Compliance:Ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines. Assist in preparing and submitting regulatory documents as needed.Study Coordination:Collaborate with principal investigators, physicians, nurses, and other healthcare professionals involved in the research. Coordinate study-related activities and scheduling.Participant Follow-up:Maintain regular contact with study participants to track their progress and ensure retention in the study.Quality Assurance:Assist in monitoring and auditing study sites to ensure protocol adherence and data quality.Adverse Event Reporting:Promptly report adverse events and safety concerns to the appropriate regulatory bodies.Job Type: Full-timePay: $12.00 - $16.00 per yearBenefits:<ul><li>Flexible schedule</li></ul>Experience:<ul><li>Clinical trials: 1 year (Preferred)</li><li>Research: 1 year (Preferred)</li></ul>Work Location: In person

Gastroenterology Associates of Central VA

Blue Ridge Medical Research, a division of Gastroenterology Associates of Central Virginia, is seeking a responsible professional for the position of Clinical Research Assistant. The research department conducts clinical trials for GI conditions with the goal of providing enhanced treatments for patients who may not get adequate relief from their current medical regimen. Our studies are conducted under the excellent care of trained physicians, nurses, and research staff, as well as monitored by the U.S. Food and Drug Administration and its affiliates.

Inside Higher Ed

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 Job Title:Clinical Research Assistant
 
 
 Department:Medicine | Psychiatry
 
 
 
 
 The university will not sponsor applicants for work visas for this position.
 
 
 
 
 The Clinical Research Assistant will provide assistance in support of clinical research studies focused on the biological mechanisms (circadian rhythms and gut-brain axis) that underlie the behavioral (and other) side effects of chemotherapy (e.g., fatigue, mood, cognitive impairment, diarrhea) in breast cancer patients; assist with implementation and coordination of studies; assist with regulatory documents; participate in recruitment of study participants; perform behavioral or diagnostic testing; retrieve stool and blood samples; perform biosample processing in our lab; assist with collection maintenance &amp; reporting of clinical research data.
 
 
 
 Minimum Required Qualifications
 
 
 
 Bachelor&rsquo;s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required. 0 years of relevant experience required. 2-4 years of relevant experience preferred.
 
 
 
 Additional Information
 
 
 
 Location:Institute for Behavioral Medicine Research (0878)
 
 
 Position Type:Term (Fixed Term)
 
 
 Scheduled Hours:40
 
 
 
 Shift:
 
 First Shift
 
 
 
 
 Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.
 
 
 
 
 Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.
 
 
 The university is an equal opportunity employer, including veterans and disability.
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Children's National Hospital

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 The Clinical Research Assistant performs a variety of research, data and clerical duties of a routine and technical nature to support the conduct of clinical research under the direction of a senior research team member. The Research Assistant will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations. In this role, the Clinical Research Assistant completes tasks including identifying eligible participants under the supervision of a senior research team member, preparing necessary documents, equipment, supplies, etc. for research visits and conducting and documenting visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments and Standard Operating Procedures (SOPs) for minimal risk studies or for other studies.
 
 
 
 Minimum Education
 
 
 
 BA/BS degree in a science, technical, health-related field or another applicable
 
 
 discipline. (Required)
 
 
 
 Minimum Work Experience
 
 
 
 0 years Experience working in a medical or scientific research setting (Preferred)
 
 
 
 Functional Accountabilities
 
 
 
 
 Responsible Conduct of Research
 
 
 
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 Consistently demonstrates adherence to the standards for the responsible conduct of research.
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 Plans, conducts and manages research projects within federal and institutional regulations and policies under the direction of the principal investigator.
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 Stays informed of and adheres to institutional policies and federal regulations (e.g. Titles 21 and 45 of the Code of Federal Regulations) and guidance (International Counsel on Harmonization) regarding human subjects research and use of protected health information.
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 Uses research funds and resources appropriately.
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 Maintains confidentiality of data as required.
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 Meets all annual job-related training and compliance requirements.
 
 
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 Research Administration
 
 
 
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 Maintains knowledge and comprehension of assigned research protocols, including study procedures, timelines and eligibility.
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 Accurately creates, completes, maintains and organizes study documents.
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 Accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.
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 Uses and accounts for research funds and resources at performance level, including reconciling research subject billing if assigned.
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 Attends study meetings, which could include overnight travel, as requested by principal investigator.
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 Works well with other members of the research team and seeks and provides input when appropriate.
 
 
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 Participant Enrollment
 
 
 
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 Adheres to the IRB-approved recruitment plan.
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 Identifies participants that meet eligibility requirements under the supervision of a senior research team member.
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 Screens subjects for eligibility per the protocol and institutional policies.
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 Communicates effectively and provides information to a diverse, vulnerable subject population in accordance with institutional policies.
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 Interacts with study participants and/or legally authorized representatives (LARs) to communicate study purpose and participation details and to assess participation interest.
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 Engages participants/LARs in the informed consent process according to institutional policies.
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 Follows procedures for documenting participant incentive distribution.
 
 
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 Study Management
 
 
 
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 Plans, conducts and manages research activities in accordance with federal regulations and guidance documents and sponsor and institutional policies under the direction of a senior study team member.
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 Conducts and documents visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments and SOPs for minimal risk studies or for other studies under direction.
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 Completes accurate IRB submissions within institutional timeframes.
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 Records participant visits in the appropriate tracking system.
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 Anticipates study needs and subject caseload in order to meet organizational objectives and deadlines in a timely manner.
 
 
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 Data Collection
 
 
 
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 Ensures data is collected as required by protocol and in accordance with research data principles (ALCOAC: Attributable, Legible, Contemporaneous, Original, Accurate and Complete).
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 Ensures that queries are resolved within sponsor and institutional timelines.
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 Plans and performs research specimen collection, labeling and storage/shipping if assigned; maintains accurate sample accountability/chain of custody documentation.
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 Ensures secure storage of study documents and assists in maintaining regulatory documents per sponsor and institutional requirements.
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 Anticipate and responds to customer needs; follows up until needs are met
 
 
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 Teamwork/Communication
 
 
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 Demonstrate collaborative and respectful behavior
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 Partner with all team members to achieve goals
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 Receptive to others&rsquo; ideas and opinions
 
 
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 Performance Improvement/Problem-solving
 
 
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 Contribute to a positive work environment
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 Demonstrate flexibility and willingness to change
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 Identify opportunities to improve clinical and administrative processes
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 Make appropriate decisions, using sound judgment
 
 
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 Cost Management/Financial Responsibility
 
 
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 Use resources efficiently
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 Search for less costly ways of doing things
 
 
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 Safety
 
 
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 Speak up when team members appear to exhibit unsafe behavior or performance
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 Continuously validate and verify information needed for decision making or documentation
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 Stop in the face of uncertainty and takes time to resolve the situation
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 Demonstrate accurate, clear and timely verbal and written communication
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 Actively promote safety for patients, families, visitors and co-workers
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 Attend carefully to important details - practicing Stop, Think, Act and Review in order to self-check behavior and performance
 
 
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 Primary Location
 
 
 
 District of Columbia-Washington
 
 
 
 Work Locations
 
 
 
 CN Hospital (Main Campus)
 
 
 
 Job
 
 
 
 Research
 
 
 
 Organization
 
 
 
 Ctr Neuroscience &amp; Behav Med
 
 
 
 Position Status
 
 
 
 R (Regular)
 
 
 
 Shift
 
 
 
 Day
 
 
 
 Work Schedule
 
 
 
 8a-4:30p
 
 
 
 Job Posting
 
 
 
 Mar 13, 2026, 12:20:28 AM
 
 
 
 Full-Time Salary Range
 
 
 
 42702.4
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The Ohio State University Wexner Medical Center

Clinical Research Assistant participates in the data collection, maintenance, and reporting, and/or patient interfacing activities for clinical and translational research studies within the Department of Otolaryngology. This role involves coordinating and performing clinical research in accordance with approved protocols, including therapeutic studies involving interventions like mindfulness, medication, or devices. Key patient-facing duties include assessing patient records to identify eligible participants, recruiting, interviewing, and enrolling patients, obtaining informed consent, and educating participants on the study process. CRA coordinates patient appointments and procedures, administers standardized diagnostic, psychological, or behavioral testing and calculates scoring, and may collect, process, and evaluate biological samples. Administrative and support tasks include assisting with the collection, entry, and maintenance of clinical research data into study databases, preparing documentation for research progress reports, completing Institutional Review Board (IRB) and sponsor study documents, and assisting with the preparation of manuscripts and grant proposals.
 
Minimum Education & Experience Required
 
Candidates must hold a bachelor’s degree in biological, health, social, or medical sciences, or possess an equivalent combination of education and experience. While no prior experience is required, 2–4 years of relevant experience is preferred. Proficient computer skills are essential. For patient‑interfacing roles, candidates must have at least one year of total experience, including a minimum of six months in a clinical support capacity and six months in a clinical research role. Requires successful completion of a background check; qualified candidates may be asked to complete a pre-employment physical, including a drug screen.
 
Regular 40 First Shift

SQRL

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 Highlights
 
 
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 Play a key role in helping patients get involved in clinical trials
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 up to $21 - $30 an hour + full benefits
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 Growth opportunities to CRC, Sr. CRC, and more!
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 Great stepping stone into research, or a way to get more experience!
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 As an Clinical Research Assistant, you will be integral to the success of our research endeavors, providing essential support throughout all phases of clinical trials. Key responsibilities include:
 
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 Assist in Start-up and Implementation Activities: Collaborate with the research team to facilitate the initiation of new studies, including protocol development and regulatory submissions.
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 Completion and Submission of Clinical Trials Amendments: Ensure timely completion and accurate submission of all amendments to the Institutional Review Board (IRB), adhering to regulatory guidelines and protocols.
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 Editing Informed Consent Documents: Review and edit informed consent documents to ensure clarity, accuracy, and compliance with regulatory standards.
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 Correspondence with Stakeholders: Serve as a primary point of contact for communication with the IRB, investigators, and sponsors throughout the clinical trial process, maintaining open lines of communication and addressing inquiries promptly.
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 Preparation of Annual Progress Reports: Compile and prepare comprehensive progress reports for IRB renewal of ongoing studies, summarizing key findings and milestones achieved.
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 Collection and Submission of Regulatory Documents: Facilitate the collection, completion, and submission of regulatory documents to various regulatory entities, ensuring compliance with regulatory requirements.
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 Maintenance of Regulatory Binders: Establish and maintain regulatory binders and other relevant files, organizing documentation meticulously during the review, approval, and activation process for clinical trials.
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 Coordination of Safety Reports: Coordinate the review and processing of safety reports to the IRB, ensuring prompt reporting and appropriate follow-up actions as required.
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 Qualifications:
 
 
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 Bachelor's degree in a relevant field (e.g., life sciences, healthcare administration, or related discipline) preferred.
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 Prior experience in clinical research or healthcare administration is preferred.
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 Experience with Phlebotomy, EKG, taking Vitals, etc. REQUIRED
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 Strong attention to detail and organizational skills.
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 Excellent written and verbal communication abilities.
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 Familiarity with regulatory requirements governing clinical research (e.g., FDA regulations, ICH-GCP guidelines) is desirable.
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 </ul>
 
 
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