Job Description

Clinical Research Physician

Clinical Research/Trial Execution and Support:

- Plans, collaborates on and reviews scientific content of clinical documents such as protocols, informed consent documents, final study reports, and submissions (for example, annual reports) according to the agreed upon project timeline.

- Provides oversight and input into ICDs

- Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review interactions).

- Review and approve risk profiles to ensure to ensure appropriate communication of risk to study subjects.

- Participate in investigator identification and selection, in conjunction with clinical teams.

- Ensure that operational team has documented the completion of administrative requirements for study initiation and conduct (for example, ethical review board, informed consent, regulatory approval/notification) consistent with Good Clinical Practices (GCPs) and local laws and requirements.

- Assist in planning process and participate in study start-up meetings and other activities to provide the appropriate training and information to investigators and site personnel.

- Serve as resource to clinical operations personnel/ clinical research monitors, investigators and ethical review boards to address any questions or clarify issues arising during the conduct of study.

- Understand and actively address the scientific information needs of all investigators and personnel.

- Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of adverse events, in alignment with corporate patient safety policies and procedures.

- Review IIT proposals and publications, as requested by Director-Medical.

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