Clinical Research Coordinator - National Harbor, MD
Oxon Hill, MD, United States11h ago
Key details
- Location
- Oxon Hill, MD, United States
- Work style
- Onsite
- Level
- Mid level
- Experience
- 2–5 yrs
- Function
- Science & Research
- Focus area
- other
- Posted
- 11h ago
Skills
ecggcpphlebotomyspecimen collection
About the role
Advanced Dermatology & Cosmetic Surgery is seeking an experienced Clinical Research Coordinator (CRC) to support clinical trials at our National Harbor location.
This is a hands-on role for a research professional with direct experience coordinating clinical studies, working with research participants, maintaining regulatory documentation, and collaborating with Principal Investigators, sponsors, and CROs.
What You'll Do
Coordinate day-to-day activities for assigned clinical trials from study start-up through closeout.
Recruit, screen, and enroll research participants according to protocol requirements.
Conduct and document the informed consent process.
Coordinate study visits, assessments, and protocol-required procedures.
Maintain accurate source documentation, regulatory binders, Case Report Forms, enrollment logs, and study records.
Assist with IRB submissions, amendments, and regulatory documentation.
Communicate with Principal Investigators, sponsors, CROs, and study participants.
Perform or coordinate vitals, EKGs, specimen collection, phlebotomy, and laboratory shipments as required by protocol.
Maintain investigational drug/device accountability and study supplies when applicable.
What We're Looking For
Previous hands-on clinical research coordination experience required.
Experience with participant recruitment, screening, informed consent, study visits, and research documentation.
Working knowledge of clinical trial protocols and inclusion/exclusion criteria.
Strong organization, accuracy, communication, and time-management skills.
Ability to manage multiple study priorities and deadlines.
Preferred Qualifications
2+ years of Clinical Research Coordinator or comparable clinical trial experience.
Experience with industry-sponsored clinical trials and pharmaceutical sponsors/CROs.
Bachelor's degree in a health science, life science, clinical research, or related field.
ACRP or SoCRA certification.
Good Clinical Practice (GCP) and IATA training.
Phlebotomy experience or certification.
Benefits?
We offer a comprehensive benefits package, including medical, dental, and vision. Ancillary coverage such as Life Ins, LTD, STD and more! Vacation and Personal Time Off Accrual and 401(k).
If you have hands-on experience coordinating clinical trials and enjoy working directly with patients, investigators, and research partners, we'd love to hear from you.
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