Disclaimer  Pre-Launch Test Posting Notice

We are seeking an experienced Clinical Project Manager (CPM) to oversee and manage clinical trials in the field of Diabetes and Metabolic Disorders. Working within a specialized CRO, the CPM will lead cross-functional teams, ensure regulatory compliance, and deliver high-quality studies on time and within budget.

disclaimer: This job posting is created for testing purposes only. The company, role, and details described are fictional and not an actual employment opportunity.

• Key Responsibilities
• Manage the planning, initiation, execution, and close-out of clinical trials in diabetes and related endocrine conditions.
• Serve as the primary point of contact for sponsors, investigators, and study teams.
• Develop project timelines, budgets, and risk management plans.
• Oversee monitoring activities to ensure compliance with ICH-GCP, regulatory guidelines, and sponsor requirements.
• Coordinate with clinical research associates (CRAs), data management, biostatistics, and pharmacovigilance teams.
• Lead project meetings, prepare progress reports, and present study updates to stakeholders.
• Support site selection, feasibility assessments, and contract negotiations.
• Identify and resolve study issues, ensuring adherence to quality standards.
• Mentor junior project staff and foster a collaborative working environment.
• Qualifications & Requirements

• Bachelor’s or Master’s degree in Life Sciences, Nursing, Pharmacy, or related field.
• Minimum 5 years of clinical research experience, with at least 2 years in project management within a CRO or pharmaceutical company.
• Previous experience managing diabetes, endocrinology, or metabolic disorder trials strongly preferred.
• Solid understanding of ICH-GCP guidelines and global regulatory requirements.
• Proven track record of successfully managing complex, multi-center clinical trials.
• Strong organizational, leadership, and communication skills.
• Ability to work in a fast-paced, deadline-driven environment.

• Working Conditions

• Office-based or remote role, with occasional travel to clinical sites, investigator meetings, or sponsor visits.
• Collaborative environment with exposure to global diabetes research programs.

• Why Join Us

• Opportunity to lead impactful clinical research in the fight against diabetes.
• Work in a CRO specialized in Endocrinology / Metabolic Disorders.
• Professional development opportunities in a supportive, team-oriented environment.

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