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Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (Cvrm))

2+ years
Not Disclosed
10 Dec. 20, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Opening: Clinical Trial Manager (Cardiovascular, Renal & Metabolic Disease)

Location: Navi Mumbai, India
Department: Clinical Trial Management
Job ID: 9656
Job Type: Full-Time

Job Summary:
Medpace is seeking an experienced Clinical Trial Manager (CTM) to lead global clinical research studies. This office-based position is located in our Navi Mumbai office. Medpace is a scientifically driven organization providing full-service support for clients, empowering project teams to lead and execute clinical trials effectively.

Responsibilities:

  • Lead global clinical trials, managing project timelines and deliverables.
  • Coordinate all contracted services for the study and manage sponsor relationships.
  • Lead cross-functional teams, including clinical monitoring, study start-up, regulatory, contracts, safety, and medical monitoring.
  • Attend bid defense meetings and assist the business development team in securing new business.

Qualifications:

  • Bachelor’s degree in a health-related field (Master’s or PhD preferred).
  • Minimum 2 years of clinical trial management experience in the Asia Pacific region, preferably in a CRO environment.
  • Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies is essential.
  • Excellent communication skills in English (both written and spoken).
  • Ability to work in a global environment with flexibility and accountability.

About Medpace:
Medpace is a full-service clinical contract research organization (CRO) offering Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, we have over 5,000 employees across 40+ countries, leveraging expertise in key therapeutic areas such as oncology, cardiology, metabolic disease, and more.

Why Medpace?

  • People. Purpose. Passion. Make a difference today to improve lives tomorrow.
  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021, 2022, 2023, 2024).
  • Awarded CRO Leadership Awards for expertise, quality, capabilities, reliability, and compatibility.

Medpace Perks:

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

How to Apply:
If you’re ready to lead clinical trials and want to work in an international and impactful environment, apply today to join Medpace.