Minerva Research Solutions Pakistan, a DRAP-licensed Clinical Research Organization affiliated with a US-based global entity, is seeking a competent and dedicated Clinical Research Associate 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:
Education:
MBBS/BDS/Pharm-D (preferred)
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
Key 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
Maintain accurate regulatory records and facilitate ethical submissions
Added Requirements:
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
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
If you are committed to improving healthcare outcomes through ethical and quality-driven research, and want to grow in a globally integrated CRO environment, we encourage you to apply.
