Associate Clinical Trial Manager - PhD / Post-Doc

Medpace Clinical Research India; Navi Mumbai; On-site; INR 600,000 - 800,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Structured career paths

Employee health and wellness initiatives

Job summary

Medpace Clinical Research India is looking for an Associate Clinical Trial Manager (aCTM) to join their team in Navi Mumbai. This position offers a fantastic opportunity for recent PhD graduates to enter the industry and develop their career. Candidates will receive extensive training and support while involved in global study activities and project management.

The ideal candidate will hold a PhD in Life Sciences, have research experiences in relevant areas, and be fluent in English. Medpace offers a competitive compensation package along with a flexible work environment.

Qualifications

• Research experience related to Cardiovascular, Renal, Metabolic or Gastrointestinal areas.
• Ability to work in a fast-paced industry with an international team.
• Prior experience within the CRO or pharmaceutical industry is advantageous.

Responsibilities

• Communicate and collaborate on global study activities.
• Ensure timely delivery of tasks with high accuracy.
• Compile and maintain project-specific status reports.

Skills

Fluency in English with solid presentation skills

Excellent organisational skills

Strong communication skills

Computer skills (word-processing, databases, Excel)

Education

PhD in Life Sciences

Job description

Title

Medpace is a leading CRO for Biotech companies and we are currently seeking candidates with PhDs and/or Post-Doctoral Research experience related to Cardiovascular, Renal, Metabolic or Gastrointestinal areas for a full-time Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in our Navi Mumbai, India office. The aCTM will be a part of the Clinical Trial Management team and support Project Coordinators and Clinical Trial Managers in performance of project management activities. Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

This is a fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

Overview

Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Responsibilities

• Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager;
• Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy;
• Compile and maintain project-specific status reports within the clinical trial management system;
• Interact with the internal project team, Sponsor, study sites, and third-party vendors;
• Provide oversight and quality control of our internal regulatory filing system;
• Provide oversight and management of study supplies;
• Create and maintain project timelines; and
• Coordinate project meetings and produce quality minutes.

Qualifications

• PhD in Life Sciences;
• Research experience related to Cardiovascular, Renal, Metabolic or Gastrointestinal areas;
• Fluency in English with solid presentation skills;
• Ability to work in a fast-paced dynamic industry within an international team;
• Prior experience within the CRO or pharmaceutical industry not required but will be advantageous; and
• Excellent computer (word-processing, databases, Excel, Windows), organisational, and communication skills.

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

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.