Clinical Research Assistant (Hybrid)

Piper Companies is seeking a detail-oriented and motivated Clinical Research Assistant to support the execution of clinical research studies in Bethesda, MD. This is an excellent opportunity for candidates interested in pursuing a career in clinical research, healthcare, biotechnology, pharmaceuticals, or medicine.

Responsibilities of the Clinical Research Assistant:

·       Assist with the day-to-day coordination and administration of clinical research studies.

·       Screen, recruit, and schedule study participants according to protocol requirements.

·       Obtain and review participant medical histories and study-related documentation.

·       Collect, process, and accurately enter clinical data into electronic data capture (EDC) systems.

·       Maintain study files, regulatory binders, and essential research documents.

·       Assist with informed consent processes and participant education under supervision.

·       Ensure compliance with FDA regulations, ICH-GCP guidelines, HIPAA requirements, and institutional policies.

Qualifications of the Clinical Research Assistant

·       0-2 years of experience in clinical research, healthcare, laboratory, or patient-facing environments

·       Previous experience supporting clinical trials or research studies.

·       Knowledge of Good Clinical Practice (GCP), HIPAA, and FDA regulations.

·       Experience with EDC systems such as Medidata Rave, REDCap, Veeva, or Oracle Clinical.

·       Experience in academic medical centers, CROs, biotechnology, or pharmaceutical environments.

·       Proficiency with Microsoft Office Suite (Excel, Word, Outlook)

·       Ability to manage multiple priorities in a fast-paced research setting.

·       Experience working with confidential patient information.

·       Bachelor’s degree in Biology, Life Sciences, Public Health, Psychology, Nursing, or a related field preferred.

Compensation of the Clinical Research Assistant:

·       Salary: Between $50,000 – $60,000 based on years of relevant experience

·       Comprehensive Benefits: Medical, Dental, Vision, 401K, Sick leave as required by law

This job opens for applications on 10/9/2026. Applications for this job will be accepted for at least 30 days from the posting date

Keywords:

Clinical Research, Research, Clinical Trial, Phase I, Research Assistant, Clinical Research Associate, Clinical Research Assistant, CRC, Clinical Research Coordinator, Research Coordinator, Biology, Medical Terminology, EMR, Electronic Medical Record, EHR, Electronic Health Record, Public Health, Medical Scribe, Medical Assistant, Healthcare, Microsoft Office, Excel, Data Entry, Data Management, Psychology, Regulatory Affairs, Regulatory, EDC, REDCap, Medical Writing, Publication, Writer, Writing, Scientific Writing, IRB, Institutional Review Board, FDA, Regulatory Submissions, IND, Investigational New Drug Application, NDA, Phase II, Phase III, Phase IV

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