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

2-4 years
Not Disclosed
10 Feb. 12, 2025
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 Title: Clinical Trial Manager (CTM) – Cardiovascular, Renal & Metabolic Disease (CVRM)

Location: Navi Mumbai, India
Job Type: Full-time, Office-based


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 an experienced Clinical Trial Manager (CTM) to lead global clinical research studies, specifically in the area of Cardiovascular, Renal, and Metabolic Disease (CVRM). This role is fully office-based in Navi Mumbai, India, and is responsible for overseeing all aspects of clinical trial execution from study initiation to completion. The CTM will manage the global clinical trials, interact with sponsors, and ensure that all project deliverables are met on time.


KEY RESPONSIBILITIES

Project Leadership & Management

  • Lead global clinical research studies, ensuring timely delivery of project milestones and meeting sponsor expectations.
  • Manage cross-functional teams including clinical monitoring, study start-up, regulatory, contracts, safety, medical monitoring, and other services contracted for the study.
  • Act as the primary point of contact for all stakeholders, including sponsors and internal project teams.
  • Ensure project timelines are adhered to, and manage deliverables for the clinical trials.
  • Attend bid defense meetings and assist the business development team in winning new business.

Study Coordination & Support

  • Coordinate all clinical trial activities, ensuring high quality and compliance with the approved protocol.
  • Oversee the management and communication with study sites and ensure the proper resources and materials are available.
  • Provide leadership to teams working on study execution and ensure the successful completion of all clinical trial phases.

QUALIFICATIONS & EXPERIENCE

Education

  • Bachelor’s degree in a health-related field (Master’s degree or PhD is preferred).

Experience

  • At least two years of experience in clinical trial management in the Asia Pacific region, ideally within a CRO environment.
  • Experience in managing Cardiovascular, Renal, and Metabolic Disease (CVRM) studies is required.

Skills & Competencies

  • Excellent communication skills, with proficiency in written and spoken English.
  • Ability to work effectively in a global environment and manage a diverse team.
  • Strong organizational skills, with the ability to handle multiple tasks simultaneously in a fast-paced environment.
  • Flexible, accountable, and detail-oriented in managing projects.

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 lead innovative clinical research studies that have a direct impact on global health.