Job Details

Key responsibilities

• Participant support: Recruit, screen, and schedule study participants. Provide education and support to participants about the study procedures.
• Data management: Collect, accurately record, and organize clinical data from source documents and case report forms. This can involve entering data into databases, transferring data from paper to digital formats, and ensuring data accuracy.
• Clinical procedures: Assist with medical examinations and procedures. Perform basic medical tests such as taking vital signs and collecting biological specimens and doing phlebotomy.
• Regulatory and protocol compliance: Ensure all research activities adhere to study protocols, GCP guidelines, and applicable regulations.
• Documentation: Prepare and maintain study-related documents, which may include drafting informed consent forms, preparing submissions, and maintaining accurate and up-to-date participant records.
• Team collaboration: Work closely with principal investigators, study coordinators, and other healthcare professionals to ensure the trial runs efficiently