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    Clinical Trial Manager ((Cardiovascular, Renal & Metabolic Disease (Cvrm))

    Medpace
    3+ 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: Clinical Trial Manager (CTM)
    Location: Office-Based in Mumbai, India

    Company Overview:

    Medpace is a leading Contract Research Organization (CRO) providing comprehensive 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, Medpace leverages its extensive regulatory and therapeutic expertise across key areas, including oncology, cardiology, metabolic diseases, endocrinology, and more. Headquartered in Cincinnati, Ohio, we employ over 5,000 professionals across 40+ countries.

    Role Summary:

    Medpace is seeking an experienced Clinical Trial Manager (CTM) to oversee global clinical research studies from our Mumbai office. This role involves leading and managing multiservice global clinical trials, coordinating with sponsors, and ensuring timely project deliverables. As a CTM, you will lead a cross-functional team and may also support business development efforts by attending bid defense meetings.

    Responsibilities:

    • Project Leadership: Act as the primary lead for multiservice global clinical trials, ensuring effective management of timelines and project deliverables.
    • Sponsor Interaction: Serve as the main point of contact for sponsors, addressing project-specific issues and ensuring client satisfaction.
    • Team Coordination: Oversee a cross-functional team including clinical monitoring, study start-up, regulatory affairs, contract management, safety, and medical monitoring.
    • Service Coordination: Ensure all contracted services for the study are effectively coordinated and executed.
    • Bid Defense Support: Attend bid defense meetings and assist the business development team in securing new business opportunities.

    Qualifications:

    • Education: Bachelor’s degree in a health-related field is required; Master’s degree or PhD is preferred.
    • Experience: Minimum of two years of clinical trial management experience, ideally in the Asia Pacific region and within a CRO environment. Experience in Cardiovascular, Renal & Metabolic Disease (CVRM) studies is required.
    • Skills: Excellent communication skills with proficiency in written and spoken English. Ability to work effectively in a global and dynamic environment.
    • Attributes: Flexible, accountable, and adept at managing complex projects in a global setting.

    Why Medpace?

    At Medpace, we are driven by a commitment to making a difference through clinical research. Our work has positively impacted countless lives, and we continue to strive towards improving health outcomes through innovative therapeutics.

    Medpace Perks:

    • Hybrid Work Options: Flexibility to work from home, based on position and experience level.
    • Competitive PTO: Generous paid time off packages.
    • Employee Benefits: Health and wellness initiatives, company-sponsored appreciation events, and flexible work schedules.
    • Career Growth: Structured career paths with opportunities for professional development and advancement.
    • Recognition: Named one of America’s Most Successful Midsize Companies by Forbes (2021-2024) and consistently honored with CRO Leadership Awards for expertise, quality, and reliability.

    Join Us:

    If you are a dedicated Clinical Trial Manager with a passion for clinical research and a track record of successful project management, we invite you to apply and be a part of our dynamic team at Medpace.

    Apply Today and help us shape the future of clinical development.

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