Associate Clinical Trial Manager

Job Description

As an Associate Clinical Trial Manager at Medpace, you will be a part of the Clinical Trial Management team in our Navi Mumbai, India office, where you will support Project Coordinators and Clinical Trial Managers in various project management activities. This role is ideal for candidates with PhDs and/or Post-Doctoral Research experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal areas who are looking to apply their analytical and academic skills in clinical project administration and management.**Responsibilities:**- Communicate and collaborate on global study activities, working closely with the project coordinator and clinical trial manager- Ensure timely delivery of recurrent tasks 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- Manage study supplies- Create and maintain project timelines- Coordinate project meetings and produce quality minutes**Qualifications:**- PhD in Life Sciences- Research experience in 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 advantageous- Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills**Medpace Overview:**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. With a mission to accelerate the global development of safe and effective medical therapeutics, we leverage local regulatory and therapeutic expertise across various areas including oncology, cardiology, metabolic disease, and more. Headquartered in Cincinnati, Ohio, we employ over 5,000 people across 40 countries.**Why Medpace :**At Medpace, we value People, Purpose, and Passion. Join us to make a difference tomorrow. With a history of positively impacting countless patients and families, we offer a flexible work environment, competitive compensation and benefits, structured career paths, employee appreciation events, and health and wellness initiatives.**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**Awards:**- Recognized by Forbes as one of Americas Most Successful Midsize Companies in 2021, 2022, 2023, and 2024- Continually recognized with CRO Leadership Awards based on expertise, quality, capabilities, reliability, and compatibility**What To Expect Next:**A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps. As an Associate Clinical Trial Manager at Medpace, you will be a part of the Clinical Trial Management team in our Navi Mumbai, India office, where you will support Project Coordinators and Clinical Trial Managers in various project management activities. This role is ideal for candidates with PhDs and/or Post-Doctoral Research experience in Cardiovascular, Renal, Metabolic, or Gastrointestinal areas who are looking to apply their analytical and academic skills in clinical project administration and management.**Responsibilities:**- Communicate and collaborate on global study activities, working closely with the project coordinator and clinical trial manager- Ensure timely delivery of recurrent tasks 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- Manage study supplies- Create and maintain project timelines- Coordinate project meetings and produce quality minutes**Qualifications:**- PhD in Life Sciences- Research experience in 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 advantageous- Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills**Medpace Overview:**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. With a mission to accelerate

Keyskills :
Project ManagementLife SciencesCardiovascularEnglishPresentation SkillsComputer SkillsCommunication SkillsClinical Trial ManagementRegulatory FilingRenalMetabolicGastrointestinal