Clinical Research Specialist

Job Title: Clinical Research Specialist

Location: Multan, Pakistan.
Job Type: Full-time, On-site
Salary: PKR 100,000 - PKR 150,000 per month

Pioneer Clinical Research in Pakistan. transform patient care.

Are you a PhD holder eager to bridge the gap between groundbreaking scientific discovery and real-world medical application? Are you looking for a role where your expertise directly shapes the future of healthcare ?

A premier Healthcare Division is seeking a highly motivated and detail-oriented Clinical Research Specialist to lead and manage our clinical trials. This is a senior role for a candidate ready to ensure scientific rigor, regulatory compliance, and the highest ethical standards in research.

Why Join Us?

• Competitive Salary & Benefits: We offer an attractive monthly salary package of PKR 100,000 to PKR 150,000.
• Lead Innovative Research: Take ownership of impactful clinical studies from concept to completion, contributing to medical advancements relevant to the Pakistani population.
• Professional Development: Gain invaluable experience in international clinical research standards and protocols. Opportunities for international training and conferences.
• Career Leadership Path: This is a high-visibility role with a clear path to senior management positions in clinical research, regulatory affairs, or medical affairs.

Key Responsibilities:

• Develop, write, and finalize detailed clinical study protocols, informed consent forms (ICFs), and case report forms (CRFs).
• Ensure all study activities comply with International Council for Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and local Drug Regulatory Authority of Pakistan (DRAP) regulations.
• Act as the main scientific liaison between the company, principal investigators, study sites, and ethics committees.
• Conduct detailed monitoring and review of clinical data for accuracy, consistency, and validity.
• Manage study timelines, budgets, and resources efficiently.
• Prepare progress reports for management and contribute to writing scientific manuscripts for publication in reputable journals.
• Train and mentor site coordinators and junior staff on protocol adherence and GCP.

Required Qualifications & Experience:

• A PhD in a Life Science field (e.g., Microbiology, Biochemistry, Pharmacology, Genetics, Public Health) from an HEC-recognized or international university.
• Minimum of 2-3 years of hands-on experience in clinical trial management/research (experience gained during PhD can be considered).
• In-depth, practical knowledge of ICH-GCP guidelines and a strong understanding of DRAP regulations.
• Exceptional analytical and problem-solving skills with a meticulous eye for detail.
• Proven scientific writing skills (protocols, reports, manuscripts).
• Fluency in English.

Preferred Qualifications:

• Experience working with CRA monitoring of Phase III or IV clinical trials.
• Prior experience in therapeutic area, e.g., Infectious Diseases, Cardiology, Diabetes.
• Existing relationships with key opinion leaders (KOLs) or investigators in Pakistan's clinical research community.
• Certification in clinical research (e.g., CCRP, CRA).

How to Apply:

Interested candidates who meet these rigorous requirements are requested to apply through Indeed.

Please submit the following:

• An updated Curriculum Vitae (CV)
• A Cover Letter explaining your interest in the role and detailing your specific experience with clinical research protocols and GCP compliance.

Apply now to lead the next wave of medical innovation.

Job Type: Full-time

Pay: Rs100,000.00 - Rs150,000.00 per month

Work Location: In person