Clinical Research Associate

About the role

Minerva Research Solutions Pakistan, a DRAP‑licensed CRO, is looking for a motivated Clinical Research Associate to support local and international clinical trials. You will act as a bridge between investigators, sponsors, and regulatory bodies, ensuring trials run smoothly and comply with all regulations.

Key responsibilities

• Manage and monitor clinical trials in line with ICH‑GCP and DRAP guidelines.
• Conduct site visits for source data verification, quality control, and compliance checks.
• Maintain accurate trial data, track drug accountability, and support logistics.
• Draft and review study documents such as protocols, informed consent forms, and monitoring reports.
• Provide training and technical support to site staff and assist with regulatory submissions.
• Support business development by engaging with international clients and sponsors.

Required profile

• MBBS, BDS or Pharm‑D (preferred) with 2–3 years of experience in clinical trial coordination.
• Strong knowledge of DRAP, ICH‑GCP, and ethical guidelines.
• Experience in quality assurance, pharmacovigilance, and regulatory submissions.
• Excellent written and spoken English and Urdu.
• Willingness to travel locally for site visits.

Required skills

• Proficiency with MS Office Suite.
• Experience using trial‑related data portals for data entry and monitoring.

What we offer

• Competitive salary package and health benefits.
• Professional development, training, and exposure to global trials.
• Supportive, inclusive workplace culture with long‑term career growth opportunities.