Clinical Research Coordinator

Roles & Responsibilities

• Actively follow up with the Institutional Review Board (IRB) for faster approval of the trial
• Ensure timely submission of all safety reports and amendments of the trial documents to the IRB

Site Initiation
• Assist in site initiation visits and ensure documentation and logistics are completed
• Maintain and manage site and patient files, including screening logs and enrollment records
• Prepare source documents and their templates
• Coordinate and schedule subject visits, including regular follow-up visits

Clinical Trial Management
• Ensure proper completion of CRFs and data entry
• Conduct meetings with investigators, sponsors, and patients
• Assist PI and Co-I in administering the informed consent form process
• Manage drug accountability and ensure compliance

Financial Responsibilities
• Maintain budget sheets for the trial
• Handle invoicing for IRB fees, site administration fees, laboratory costs, and study subject reimbursements

Qualification

• Bachelor of Science or MSc

Experience

• 0 - 1 years of experience in clinical research

Vacancies

• 1 opening

Skills

• Strong attention to detail and organizational skills
• Ability to manage multiple tasks and deadlines
• Excellent communication and interpersonal skills
• Knowledge of clinical research processes and regulatory guidelines
• Ability to work well with cross-functional teams

About The Company

Max Super Speciality Hospital is a renowned healthcare institution offering a wide range of medical services. With state-of-the-art facilities and a commitment to high-quality patient care, the hospital is known for its excellence in clinical research, particularly in the areas of clinical trials and new drug development. As a Clinical Research Coordinator at Max Healthcare, you will contribute to cutting-edge clinical research while working in a dynamic, patient-focused environment