We are looking for candidates with medical backgrounds and excellent interpersonal skills for the position of clinical research coordinator. Clinical research coordinators are responsible for conducting clinical research trials by adhering to Good Clinical Practice (GCP), International Air Transportation (IATA) and FDA regulations. The candidate will be performing required visit procedures, administering questionnaires and subject material, adhering to regulatory trial standards, and participating in subject recruitment efforts, among other duties.
Clinical research coordinators need to engage with the research investigators, pharmaceutical companies (sponsors) and contract research organizations (CROs) as well as the research subjects requiring excellent interpersonal and communicative skills.
Clinical Research Coordinator Responsibilities:
- Overseeing the smooth running of clinical trials.
- Performing clinic visits as per the protocol, GCP and FDA
- Completing procedures such as phlebotomy, EKGs Vitals, assessments
- Collecting and entering data obtained for the trial
- Informing participants about study objectives.
- Administering questionnaires.
- Monitoring research participants to ensure adherence to study rules.
- Adhering to research regulatory standards.
- Adhering to ethical standards.
- Maintaining detailed records of studies as per FDA guideline and regulatory documentation
- Managing investigational medication including receiving, dispensing, storing and performing accountability
- Liaising with laboratories process, ship and ensure investigators review reports
- Participating in subject recruitment efforts.
- Ensuring that the necessary supplies and equipment for a study are in stock and in working order.
- Engaging with subjects and understanding their concerns and managing the visit flow as indicating in the protocol.
- All other job duties as assigned by the Department Manager.