Research Assistant (Clinical)
About The Position
This role involves a combination of clinical and research responsibilities to support clinical studies. The Research Assistant will be involved in patient-facing duties such as obtaining vital signs, performing venipuncture, processing laboratory specimens, and conducting ECGs. They will also be responsible for accurate data entry into electronic systems, maintaining source documentation, and assisting with informed consent processes. Additionally, the role requires adherence to Good Clinical Practice (GCP), Institutional Review Board (IRB), HIPAA, and institutional policies, including participation in regulatory activities and maintaining necessary certifications.
Requirements
- Hands‑on clinical experience performing: Vital signs
- Hands‑on clinical experience performing: Venipuncture / blood draws
- Hands‑on clinical experience performing: Laboratory specimen processing
- Hands‑on clinical experience performing: ECGs
- High school diploma or equivalent required
- Prior experience in clinical research, healthcare, or medical assistant roles
- Strong attention to detail and documentation accuracy
- Basic computer proficiency and data entry experience
- Ability to work independently and as part of a multidisciplinary team
Nice To Haves
- Associate’s or Bachelor’s degree in health sciences, life sciences, or related field preferred
- Medical Assistant certification (CMA, RMA, or equivalent)
- GCP certification
- Experience with EDC/eSource systems (e.g., CRIO, Medidata)
- Prior experience in industry‑sponsored clinical trials
- Phlebotomy certification
Responsibilities
- Obtain and document vital signs (blood pressure, heart rate, temperature, respiratory rate, height, weight) per protocol
- Perform venipuncture and blood draws for research studies
- Process, label, centrifuge, store, and ship laboratory specimens according to protocol and laboratory manuals
- Perform 12‑lead ECGs and ensure accurate transmission and documentation
- Prepare exam rooms and maintain clinical supplies for study visits
- Assist with participant flow during research visits and ensure patient comfort and safety
- Accurately enter clinical and study data into electronic data capture (EDC) systems and/or study databases
- Maintain source documentation that is complete, accurate, and audit‑ready
- Assist with informed consent discussions and documentation, as directed
- Support study visits, screenings, and follow‑ups according to protocol schedules
- Identify and promptly report protocol deviations, adverse events, and data discrepancies to the study team
- Follow GCP, IRB, HIPAA, and institutional policies
- Assist with study regulatory binders and document maintenance
- Participate in monitoring visits, audits, and inspections as needed
- Maintain required certifications and training
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
