Associate Clinical Trial Manager - PhD/Post-Doc (Cardiovascular, Renal & Metabolic Disease)
Location: Navi Mumbai, India
Position: Associate Clinical Trial Manager (aCTM)
Job ID: 9657
Job Summary:
Medpace, a leading CRO for biotech companies, is seeking recent PhD or Post-Doctoral candidates for the position of Associate Clinical Trial Manager (aCTM). This role is based in our Navi Mumbai office and offers an exciting opportunity for individuals looking to transition into the clinical research field. The aCTM will work alongside Clinical Trial Managers and Project Coordinators to manage and support clinical trial activities, particularly in the area of Cardiovascular, Renal, and Metabolic Diseases (CVRM).
This is an excellent chance to apply your academic and analytical expertise in a clinical project administration setting and develop a career in the research and development of cutting-edge therapeutics.
What We Offer:
Training & Career Growth: Intensive foundational training and an accelerated career path in Clinical Trial Management (CTM).
International Environment: Work in a dynamic global setting, collaborating with project teams, sponsors, and study sites.
Competitive Compensation: Salary and benefits package tailored to the role.
Perks: Flexible work environment, health and wellness initiatives, employee appreciation events, and structured career development opportunities.
Responsibilities:
Collaboration: Work closely with project coordinators, clinical trial managers, and global teams to ensure smooth execution of study activities.
Project Management: Compile and maintain project-specific status reports, ensuring all tasks are completed with high accuracy and on time.
Regulatory Filing: Oversee and manage the internal regulatory filing system, ensuring compliance.
Study Supplies Management: Ensure timely procurement and management of study supplies.
Timeline & Meetings: Create and maintain project timelines, coordinate meetings, and produce high-quality minutes.
Qualifications:
Education: PhD in Life Sciences (preferably in Cardiovascular, Renal & Metabolic Diseases).
Experience: Prior experience within the CRO or pharmaceutical industry is advantageous but not required.
Skills: Strong computer skills (Word, Excel, databases), organizational skills, and the ability to work in a fast-paced, international environment.
Communication: Fluent in English with solid presentation skills.
Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO) that offers Phase I-IV clinical development services. We specialize in a wide range of therapeutic areas, including oncology, cardiology, metabolic disease, endocrinology, and more. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries.
Why Medpace?:
Recognized by Forbes as one of America's Most Successful Midsize Companies (2021, 2022, 2023, 2024).
Continually awarded CRO Leadership Awards by Life Science Leader magazine.
Join a company that makes a significant difference in the lives of patients across a variety of diseases.
Medpace offers a competitive environment for career growth, supported by ongoing employee initiatives and a commitment to excellence in clinical research.
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