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Associate Clinical Trial Manager - Phd / Post-Doc ((Cardiovascular, Renal & Metabolic Disease (Cvrm))

2+ years
Not Disclosed
10 Dec. 17, 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 Title: Associate Clinical Trial Manager - PhD/Post-Doc (Cardiovascular, Renal & Metabolic Disease)
Location: Navi Mumbai, India
Job Type: Full-time

Job Summary:
Medpace is a leading Contract Research Organization (CRO) catering to biotech companies, and we are looking for a motivated Associate Clinical Trial Manager (aCTM) with a PhD or Post-Doctoral research experience to join our Clinical Trial Management team in Navi Mumbai, India. The aCTM will work alongside Project Coordinators and Clinical Trial Managers to support project management activities. This is an excellent opportunity for recent PhD graduates to transition into the clinical research industry, gain foundational training, and develop a career in clinical trial management.

Responsibilities:

  • Collaborate with global teams, including the project coordinator and clinical trial manager, on study activities.
  • Ensure the timely delivery of tasks with a high degree of accuracy.
  • Maintain project-specific status reports within the clinical trial management system.
  • Coordinate with internal teams, sponsors, study sites, and third-party vendors.
  • Oversee and manage the internal regulatory filing system.
  • Supervise study supplies management.
  • Create and maintain project timelines and coordinate project meetings.
  • Document and produce quality minutes for project meetings.

Qualifications:

  • PhD in Life Sciences.
  • Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) is required.
  • Fluency in English with strong presentation and communication skills.
  • Ability to work effectively in a fast-paced, dynamic international environment.
  • Prior experience in the CRO or pharmaceutical industry is advantageous but not required.
  • Proficiency in computer programs (Word, Excel, databases, Windows) and strong organizational skills.

Medpace Overview:
Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services across various therapeutic areas, including oncology, cardiology, metabolic disease, and more. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 people across 40+ countries.

Why Medpace?

  • People. Purpose. Passion. We are committed to making a difference in tomorrow’s healthcare.
  • Awards: Recognized by Forbes as one of America’s Most Successful Midsize Companies in 2021, 2022, 2023, and 2024.
  • Continually awarded with CRO Leadership Awards for expertise, quality, capabilities, and reliability.

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