Instagram
youtube
Facebook

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

Location: Navi Mumbai, India
Department: Clinical Trial Management
Job ID: 9657
Job Type: Full-Time

Job Summary:
Medpace, a leading CRO for biotech companies, is seeking a full-time Associate Clinical Trial Manager (aCTM) with a PhD or Post-Doctoral research experience in Cardiovascular, Renal & Metabolic Disease (CVRM). The aCTM will be part of the Clinical Trial Management team, supporting project coordinators and clinical trial managers in project management activities. This role offers an excellent opportunity for recent PhD graduates to apply academic skills in clinical project administration and management.

Responsibilities:

  • Collaborate on global study activities, working closely with the project coordinator and clinical trial manager.
  • Ensure timely and accurate completion of recurrent tasks.
  • Compile and maintain project-specific status reports within the clinical trial management system.
  • Interact with internal teams, sponsors, study sites, and third-party vendors.
  • Provide oversight and quality control for regulatory filing systems.
  • Manage study supplies and ensure project timelines are met.
  • Coordinate project meetings and produce detailed minutes.

Qualifications:

  • PhD in Life Sciences (Cardiovascular, Renal & Metabolic Disease experience is required).
  • Fluency in English with strong presentation skills.
  • Ability to work in a fast-paced, dynamic industry with an international team.
  • Prior experience in a CRO or pharmaceutical industry is a plus, but not required.
  • Proficiency in computer applications (Word, Excel, databases) and excellent organizational and communication skills.

About Medpace:
Medpace is a full-service clinical contract research organization (CRO) that provides Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. With over 30 years of experience, we are committed to accelerating the global development of safe and effective medical therapeutics.

Why Medpace?

  • People. Purpose. Passion. Make a difference today and 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 are ready to start your career in clinical trial management and want to work in an international environment, apply today to join Medpace.