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Research Trial Manager
3 weeks ago
We are seeking a dedicated and experienced Clinical Research Coordinator to join our team.
- Job Summary:
- The successful candidate will be responsible for managing and monitoring clinical trials in compliance with international and local regulations.
- Key Responsibilities:
- Manage and monitor clinical trials ensuring adherence to regulatory requirements;
- Conduct regular site visits for source data verification and quality control;
- Maintain accurate records of trial data, ensuring accuracy and integrity;
- Coordinate with investigators, sponsors, CTUs, IRBs, and regulatory authorities;
- Draft and review study documents including protocols, informed consent forms, and reports;
- Assist in drug accountability, supplies logistics, and documentation;
- Provide training and technical support to site staff as required;
- Support business development efforts through international client engagement;
- Requirements:
- Minimum 2-3 years of experience in clinical trial coordination, CROs, CTUs, hospitals, or pharmaceutical companies;
- Strong understanding of DRAP, ICH-GCP, and ethical guidelines governing clinical research;
- Previous experience in Quality assurance in data integrity, pharmacovigilance, regulatory submissions, and stakeholder coordination;
- Benefits:
- Competitive salary package;
- Health and wellness benefits;
- Professional development and training support;
- Opportunities to work on global trials and with international sponsors;
- Supportive and inclusive workplace culture;
- Exposure to regulatory, data management, and quality assurance practices;
- Company-sponsored events and learning opportunities;
- Long-term career growth in clinical research;
