Company: Minerva Research Solutions Pakistan (A DRAP-Licensed CRO)
Location: Head Office – Karachi
Job Status: Full-time, On-site
Schedule: Monday to Friday | 9:00 AM to 5:00 PM Job Description:
Minerva Research Solutions Pakistan, a DRAP-licensed Clinical Research Organization affiliated with a US-based global entity, 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.
Experience and Qualification:
Location: Head Office – Karachi
Job Status: Full-time, On-site
Schedule: Monday to Friday | 9:00 AM to 5:00 PM Job Description:
Minerva Research Solutions Pakistan, a DRAP-licensed Clinical Research Organization affiliated with a US-based global entity, 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.
Experience and Qualification:
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Education:
- Pharm-D (preferred)
- MBBS
- BDS
-
Experience:
- 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
-
Certifications:
- Clinical Research Certification (such as ACRP) preferred
- 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
- Maintain accurate regulatory records and facilitate ethical submissions
- Excellent command of English and Urdu (spoken and written)
- Proficient in MS Office Suite and trial-related data portals
- Strong interpersonal, communication, and presentation skills
- Confident, organized, deadline-driven, and eager to learn
- Willingness to travel locally for site visits and meetings
- Strong sense of ethics, confidentiality, and responsibility
- 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
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