Job Description:

A Clinical Research Coordinator manages and oversees clinical trials and research studies. Responsibilities include:

• Study Management: Coordinate and administer clinical trials, ensuring adherence to protocols and regulatory requirements.
• Participant Interaction: Recruit, screen, and enroll study participants, and manage their care throughout the trial.
• Data Collection: Collect, record, and manage data from study participants, ensuring accuracy and confidentiality.
• Compliance: Ensure compliance with ethical standards, Good Clinical Practice (GCP), and regulatory guidelines.
• Reporting: Prepare and submit study documentation and progress reports to sponsors and regulatory agencies.
• Team Collaboration: Work closely with investigators, medical staff, and other team members to facilitate smooth study operations.

Qualifications:

• Bachelor’s degree in life sciences or related field (or equivalent experience).
• Experience in clinical research or a related field is preferred.
• Strong organizational and communication skills.

Work Environment:

Clinical Research Coordinators work in research institutions, hospitals, or clinical trial sites, often managing multiple studies and interacting with diverse teams and participants.