Clinical Trial Manager

Há 4 dias

Rio de Janeiro, Rio de Janeiro, Brasil beBeeCareer Tempo inteiro

Therapeutic Progress Advancement

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  • Job Description: We are seeking a highly skilled professional to manage one or more clinical trials across assigned countries. The ideal candidate will ensure compliance with regulations, Good Clinical Practice, and technical protocols aligned with study objectives, timelines, and budgets.
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  • Responsibilities:
    Collaborate on Study Country Prospections
    Assess feasibility of assigned studies, including country and center assessments
    Manage local/regional studies
    Plan, manage, and oversee clinical trial activities across all phases (preparation, recruitment, follow-up, closure), including administration, budgeting, regulatory compliance, logistics, contracts, and training
    Ensure compliance with regulations, GCP, and applicable guidelines
    Contribute to and ensure technical knowledge within the study team
    Supervise monitoring and management activities by subcontractors
    Support audits and inspections, lead CAPA resolutions
    Organize and conduct investigator meetings locally and regionally
    Identify, assess, mitigate, and escalate risks or issues as needed
    Define resource needs for studies
    Coordinate specific activities or manage departmental tasks as delegated by the Director.
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  • Requirements:
    Mid-Senior level employment type
    Full-time job function Project Management and Information Technology Industries Pharmaceutical Manufacturing Referrals can double your chances of interviewing at Servier.
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  • Benefits:
    Join teams recognized for scientific excellence and develop your full potential in a supportive environment with onboarding, mobility opportunities, quality training, responsible management, and a focus on well-being.
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  • Why Choose Us:
    At our company, we value commitment because we know that to achieve great results, dedication is essential. Here, growth is a journey shared through knowledge, experiences, and achievements, always daring to innovate.
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  • Key Skills and Qualifications:
    Strong understanding of Good Clinical Practice and regulatory requirements
    Excellent communication and collaboration skills
    Ability to work independently and as part of a team
    Strong problem-solving and analytical skills
    Proficient in project management tools and software
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Join us and be part of a team that makes a difference.

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