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    Associate Director, Clinical Trial Management – Remote

    Medpace
    5+ years
    Not Disclosed
    North Carolina Raleigh
    10 Feb. 12, 2025
    Job Description
    Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills:

    Job Title: Associate Director, Clinical Trial Management – Remote

    Location: Raleigh, North Carolina (Remote flexibility available for candidates with relevant experience)
    Job Type: Full-time

    ABOUT MEDPACE

    Medpace is a leading full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. We leverage our local regulatory and therapeutic expertise across key therapeutic areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, and anti-viral and anti-infective.
    Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals in more than 40 countries.

    JOB SUMMARY

    Medpace is seeking an experienced Associate Director, Clinical Trial Management to join our Clinical Trial Management team. This role will oversee the day-to-day management of global clinical trials, ensuring adherence to protocols and regulations while interacting with sponsors and leading internal project teams. The position offers remote flexibility for candidates with relevant experience.

    KEY RESPONSIBILITIES

    Project Leadership & Oversight

    • Manage day-to-day operations of clinical trials as per contract, adhering to ICH/GCP guidelines and applicable laws and regulations.
    • Serve as the primary sponsor contact for operational issues and study deliverables, ensuring clear communication and timely resolution.
    • Maintain in-depth knowledge of the protocol, therapeutic area, and study indication to ensure proper execution of clinical trials.
    • Provide cross-functional oversight of internal project teams, ensuring all team members receive necessary project-specific training.
    • Review and provide input for study protocols, edit check specifications, data analysis plans, and final study reports.
    • Develop operational project plans and manage risk assessments, ensuring smooth project execution.
    • Manage study vendors where applicable, ensuring deliverables meet quality standards and timelines.
    • Oversee site quality, providing direct supervision of project-related monitoring and deliverables.

    QUALIFICATIONS & EXPERIENCE

    Education

    • Bachelor’s degree in a health-related field required; Advanced degree in a health-related field is preferred.

    Experience

    • At least 5 years of experience as a Project/Clinical Trial Manager within a CRO environment, managing clinical trials in Phases 1-4 (with a preference for Phases 2-3).
    • Experience managing overall project timelines and project deliverables.
    • Bid defense experience is preferred.

    Skills & Competencies

    • Strong leadership skills with a track record of leading cross-functional teams and driving project success.
    • Excellent communication skills, both written and verbal, with the ability to effectively communicate with sponsors and internal teams.
    • Strong problem-solving skills and ability to make decisions in a fast-paced environment.
    • Ability to manage multiple projects simultaneously and navigate a dynamic work environment.

    COMPENSATION & BENEFITS

    • Competitive salary/bonus program.
    • Equity grants available.
    • Flexible work environment and remote work options for the right candidate.
    • Comprehensive benefits package, including health, dental, and vision coverage.
    • Paid time off (PTO), starting at 20+ days.
    • Employee health and wellness initiatives.
    • Company-sponsored appreciation events and employee recognition programs.
    • Discounts for local businesses.

    AWARDS & RECOGNITION

    • Forbes: Recognized as one of America's Most Successful Midsize Companies (2021, 2022, 2023, and 2024).
    • CRO Leadership Awards from Life Science Leader magazine for excellence in expertise, quality, capabilities, reliability, and compatibility.

    WHY MEDPACE?

    Medpace is a purpose-driven company, committed to improving patient lives through the development of cutting-edge therapeutics. Join us and become part of a collaborative team working to drive global health solutions forward.

    HOW TO APPLY

    Apply now to become part of Medpace's Clinical Trial Management team and contribute to leading impactful clinical trials globally.

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    Bucharest |

    Makkah :

    Rabigh | Khulais | Riyadh | Najran | Jeddah | King Abdullah Economic City |

    Nišava District :

    Niš |

    Singapore :

    Singapore |

    South Africa :

    South Africa | Midrand |

    Brazil :

    Sao paulo | Brazil |

    South America :

    Argentina | Peru |

    Catalonia :

    Barcelona |

    Madrid :

    Madrid |

    Sweden :

    Sweden |

    Taipei :

    Taipei |

    Williamson :

    Brentwood |

    Republic of Thailand :

    Bangkok |

    Kyiv Oblast :

    Kyiv |

    Dubai :

    Dubai |

    Hà Nội :

    Hà Nội | Hanoi |

    Ho Chi Minh :

    Ho Chi Minh City |