Clinical Research Executive

Job Description:

Responsibilities

• Coordinate with Principal Investigators (PIs), Institutional Review Boards (IRB), Sponsors/CROs, and research teams to execute clinical trials.
• Recruit and follow up with trial participants to ensure their well-being throughout the study.
• Maintain trial databases, logs, and documentation for regulatory compliance.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and applicable regulatory requirements.
• Train staff on trial-related duties and ethical considerations in clinical research.
• Protect the rights and confidentiality of all trial participants.
• Ensure timely and accurate reporting of trial data, including adverse events and protocol deviations.
• Manage documentation, including informed consent forms, Case Report Forms (CRFs), and other regulatory submissions.
• Archive trial-related documents for the required retention period.
• Identify potential research opportunities and liaise with sponsors.  

Qualification

• Bachelors/Masters in Life Sciences w/ Certificate course in Clinical Research, OR
• Bachelors/Masters in Clinical Research
• Excellent written and oral communication skills.
• Preference for ICH-GCP trained professional.