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Clinical Research Assistant

Excell Research
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The Clinical Research Assistant (CRA) will support the Principal and Sub-Investigators, Executive Site Lead, Study Coordinators, and other site staff in executing daily clinical trial tasks. Under supervision, the CRA will assist with various responsibilities related to the preparation, conduct, and administration of clinical trials. The CRA plays a vital role in ensuring compliance with study protocols, GCP, ICH Guidelines, and standard operating procedures.

 

Key Responsibilities:

-Assist in conducting clinical trials according to study protocols, Good Clinical Practice (GCP), ICH Guidelines, and our Standard Operating Procedures (SOPs).                                                           

-Understand and support the informed consent process, ensuring ongoing consent from study participants.

-Perform venipuncture, capillary puncture, and other specimen collection tasks within the scope of the protocol and legal regulations.
-Under supervision, conduct clinical assessments such as vital signs, phlebotomy, ECG, and other assessments as required by the protocol.
-Process, package, and ship laboratory specimens per protocol and IATA regulations.
-Track, order, and maintain inventory of study supplies throughout the clinical trial.
-Assist with front-office duties, including scheduling participants, making reminder calls, and updating tracking systems.
-Submit requests for the release of medical and pharmacy records as necessary.
-Apply good documentation practices while collecting and transferring data to sponsor or CRO data capture systems, resolving queries under the direction of the Clinical Research Coordinator.
-Prepare source document charts, copy, and file medical records and study-related documents as required.
 

Growth Opportunity:  After successfully working for a time as a Clinical Research Assistant, employees may have the opportunity to transition to the Clinical Research Coordinator (CRC) role, depending on their skills and our needs.

Work Hours: Monday-Friday 8:30am-5:00pm, with potential for occasional travel or work outside of office hours.