
Global Clinical Research Operations Manager
4 days ago
Minerva Research Solutions Pakistan is seeking a competent and dedicated Clinical Trial Research Coordinator. The ideal candidate will possess extensive knowledge of clinical trial operations and regulatory frameworks, along with hands-on experience in site coordination, protocol compliance, and cross-functional collaboration in the pharmaceutical and healthcare research ecosystem.
This role demands proactive communication, strong documentation practices, and coordination with investigators, sponsors, and regulatory bodies to ensure smooth conduct of local and international trials.
Responsibilities:
- Manage and monitor clinical trials in compliance with international (ICH-GCP) and local (DRAP) regulations
- Conduct regular site visits for source data verification and quality control
- Maintain and track clinical 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
Required Skills and Qualifications:
- Education: Pharm-D (preferred), MBBS, BDS
- Experience: 2–3 years in clinical trial coordination, CROs, CTUs, hospitals, or pharmaceutical companies
- Understanding of DRAP, ICH-GCP, and ethical guidelines governing clinical research
- Certification: Clinical Research Certification (such as ACRP) preferred
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
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