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    Associate Clinical Trial Manager

    Medpace
    2+ years
    Preffered by Company
    Mumbai
    10 Aug. 26, 2024
    Job Description
    Job Type: Full Time Education: B.Pharm/ M.Pharm/ B.Sc/ M.Sc/Any 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 (aCTM)
    Location: Navi Mumbai, India

    Company Overview:

    Medpace is a leading Contract Research Organization (CRO) that specializes in providing comprehensive Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to advance the global development of safe and effective medical therapeutics through a rigorous, scientific approach. With over 5,000 employees across 40+ countries, we offer a dynamic and international environment for career growth.

    Role Summary:

    Medpace is seeking a highly motivated Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team in Navi Mumbai. This role is ideal for recent PhD graduates or those with post-doctoral research experience who are looking to transition into clinical project management. The aCTM will support Project Coordinators and Clinical Trial Managers by engaging in various project management activities, gaining valuable industry experience, and contributing to the successful execution of global clinical trials.

    Responsibilities:

    • Global Collaboration: Work closely with the Project Coordinator and Clinical Trial Manager to communicate and collaborate on global study activities.
    • Task Management: Ensure timely and accurate delivery of recurrent tasks.
    • Reporting: Compile and maintain project-specific status reports within the clinical trial management system.
    • Stakeholder Interaction: Liaise with internal project teams, sponsors, study sites, and third-party vendors.
    • Quality Control: Oversee and maintain quality control of internal regulatory filing systems.
    • Study Supplies: Manage and oversee study supplies and resources.
    • Project Timelines: Create and maintain detailed project timelines.
    • Meeting Coordination: Organize project meetings and produce high-quality minutes.

    Qualifications:

    • Education: PhD in Life Sciences required.
    • Experience: Experience in Cardiovascular, Renal, and Metabolic Diseases (CVRM) preferred.
    • Skills: Strong fluency in English with excellent presentation skills; proficiency in computer applications including word processing, databases, and Excel.
    • Attributes: Ability to thrive in a fast-paced, international environment; prior experience in a CRO or pharmaceutical setting is advantageous but not required.

    Why Medpace?

    Medpace is committed to making a difference through clinical research, positively impacting patients' lives globally. Join our team to be part of a mission-driven organization with a focus on improving health outcomes and advancing medical science.

    Medpace Perks:

    • Work Flexibility: Hybrid work-from-home options based on position and experience.
    • Competitive PTO: Generous paid time off packages.
    • Employee Benefits: Health and wellness programs, company-sponsored appreciation events, and a flexible work schedule.
    • Career Development: Structured career paths with opportunities for professional growth and advancement.
    • Recognition: Named one of America’s Most Successful Midsize Companies by Forbes (2021-2024) and honored with CRO Leadership Awards from Life Science Leader magazine for expertise, quality, and reliability.

    Apply Today:

    If you are a recent PhD graduate with a passion for clinical research and project management, we invite you to apply for the Associate Clinical Trial Manager position and join our dedicated team at Medpace.

    Make a Difference Tomorrow. Join Us Today.

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