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Key Responsibilities:
- Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.
- Oversees scheduling of study participant appointments and serves as the patient liaison to the PI and other participating clinicians
- Reviews and comprehends each assigned protocol including study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections.
- Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all questions pertaining to the study posed during the informed consent process.
- Support development of clinical study budgets based on proposed study protocols.
- Coordinates and attends sponsor and monitor visits
- Responds to data clarification requests in a timely manner.
- Participate in Investigator meetings requiring travel and report pertinent information back to research team members.
- Coordinates with PIs and department to help ensure that clinical research and related activities are performed in accordance with sponsoring agency policies and procedures.
- Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan.
- Maintains records and other documentation of training.
- Maintains subject screening logs and protocol deviation logs.
- Maintains a spreadsheet tracking updates to database of all subjects enrolled on clinical studies.
- Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by IRB’s, Regulatory agencies, CRO’s and sponsors.
- Collaborates with PI and institution to respond to any audit findings and implement-approved recommendations.
- Ensures that all materials for each clinical trial protocol are available for subject enrollment
- Works collaboratively with the other members of the clinical research team and the clinical and administrative support teams to ensure all protocols are followed and that there is timely documentation and submission of study data.
- Establishes and organizes study files, including but not limited to, regulatory binders, study specific source documentation and other materials as required.
- Arranges secure storage of study documents that will be maintained according to institutional policy or for the contracted length of time, whichever is longer
- May perform other job related duties as requested or required Knowledge of program management
- Oversees regulatory submissions and approvals to local and international institutional review boards or ethical review committees
- Familiar with the diverse needs of clinical studies
Application Procedure:
To apply for this post you must be a registered user. Log into your account then go to Vacancies, view the post and click on the button: “Apply for this job”.
- Candidates must supply an email and telephone contact that will be used when offering interviews. Only shortlisted candidates will be contacted. Shortlisted candidates shall be required to produce ORIGINALS of their National Identity Card, academic and professional certificates, original transcripts and testimonials, detailed curriculum vitae and valid clearance certificate (certificate of good conduct) during the interviews.
