Associate Clinical Trial Manager - Phd / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (Cvrm))
Job Description
Job Title: Associate Clinical Trial Manager (aCTM) – PhD/Post-Doc (Cardiovascular, Renal & Metabolic Disease)
Location: Navi Mumbai, India
Job Type: Full-time
ABOUT MEDPACE
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across key areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, and anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries.
JOB SUMMARY
Medpace is seeking PhD or Post-Doctoral Research candidates to join our Clinical Trial Management team as Associate Clinical Trial Managers (aCTM). This role is located in Navi Mumbai, India, and offers an opportunity for recent PhD graduates to gain foundational training and enter the clinical research industry. The aCTM will support Project Coordinators and Clinical Trial Managers (CTMs) in managing global clinical trials with a focus on Cardiovascular, Renal & Metabolic Disease (CVRM). This position provides an accelerated career path for those interested in transitioning their academic and analytical skills into clinical project management.
KEY RESPONSIBILITIES
Study Coordination & Communication
- Collaborate with global study teams, including Project Coordinators, CTMs, study sites, and third-party vendors.
- Ensure timely delivery of project tasks, maintaining a high level of accuracy and quality.
- Coordinate project meetings and produce accurate meeting minutes.
- Compile and maintain project-specific status reports within the clinical trial management system.
Regulatory & Study Management
- Provide oversight and quality control for the internal regulatory filing system.
- Manage and track study supplies, ensuring they are appropriately distributed and maintained.
- Develop and maintain project timelines to ensure the project stays on track.
Project Support & Administration
- Support the clinical trial management team by overseeing project-related activities, contributing to the success of clinical trials.
- Ensure high levels of communication within the internal project team, sponsors, and study sites.
QUALIFICATIONS & EXPERIENCE
Education & Experience
- PhD in Life Sciences (or related field).
- Experience or research background in Cardiovascular, Renal, and Metabolic Disease (CVRM) is preferred.
- Prior experience in the CRO or pharmaceutical industry is advantageous but not required.
Skills & Competencies
- Fluency in English, with strong presentation and communication skills.
- Ability to work in a fast-paced, dynamic industry and collaborate within an international team.
- Proficient in computer skills (Word-processing, databases, Excel, Windows).
- Strong organizational skills and ability to manage multiple tasks simultaneously.
COMPENSATION & BENEFITS
- Competitive compensation and benefits package.
- Competitive PTO packages with ample vacation time.
- Structured career paths with opportunities for professional growth.
- Employee wellness initiatives, including health and wellness programs.
- Company-sponsored employee appreciation events.
AWARDS & RECOGNITION
- Forbes: Recognized as one of America's Most Successful Midsize Companies (2021, 2022, 2023, and 2024).
- CRO Leadership Awards from Life Science Leader magazine for expertise, quality, capabilities, reliability, and compatibility.
WHY MEDPACE?
At Medpace, we are passionate about making a difference in the lives of patients through cutting-edge therapeutics. Our work has positively impacted countless patients and families across a variety of therapeutic areas.
Join us and be part of a team that transforms research into real-world solutions.
HOW TO APPLY
Apply now to become part of Medpace's Clinical Trial Management team and launch your career in clinical research management.
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