Benefit-Risk Excellence Lead (Sr PV Manager) - client-dedicated for 12 months

    Remote, Serbia
    Full-Time
    Senior (7+ yrs)
    Legal & Compliance
    Leadership
    Posted on August 11, 2026

    Work Schedule

    Standard (Mon-Fri)

    Environmental Conditions

    Office

    Job Description

    Benefit-Risk Excellence Lead

    The Benefit–Risk Excellence Lead will deliver short- and mid-term projects

    that drive innovation and excellence within the Benefit–Risk Assessment &

    Management (BRAMS) function. This includes enhancing procedures and

    supporting digital transformation (automation and AI) This includes leading

    transformational projects and supporting the implementation of project

    outcomes (e.g., process/ SOP changes, etc.) within the signal detection and

    safety writing systems.

    The role requires significant experience in signal detection and safety writing

    with strong industry and regulatory knowledge.

    Key Responsibilities

    • Governance, operating model, and portfolio prioritization support

    • Executive stakeholder alignment and strategic decision support

    • Transformation planning and roadmap development

    • Initiative escalation and risk management

    • Oversight across the portfolio

    • Business case review

    • Initiative mobilization support

    • Business analysis and requirements gathering

    • Support for Signal Detection and Benefit-Risk initiatives

    • Process assessment and documentation

    • Translation of business needs into system and process requirements

    • Reporting, visualization, and documentation support

    • Coordination between business stakeholders and technology teams

    • Workshop planning and follow-up

    • Day-to-day execution support

    Required Skills & Experience

    • Relevant Life-Sciences Bachelors Degree

    • >10 years of biopharmaceutical industry experience, with significant

    hands-on expertise in signal detection, safety writing, and risk

    management across the full drug development lifecycle.

    • Strong knowledge of global GCP and GVP regulations, industry

    standards, and evolving regulatory expectations.

    • Proven change-leadership experience, including identifying needs,

    designing and implementing creative solutions, leading teams through

    transitions, and monitoring outcomes to ensure value delivery.

    • Demonstrated adaptability and resilience, maintaining progress and

    stability in dynamic or challenging environments.

    • Excellent communication skills, including clear and articulate verbal,

    written, and presentation abilities, with strong command of English

    language.

    • Ability to work independently, manage multiple priorities, and

    collaborate effectively in a matrixed organisation.

    Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

    Apply today! http://jobs.thermofisher.com

    Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

    Enables customers to make the world healthier, cleaner and safer through life sciences research, analytical challenges, and diagnostics.
    10001+ employees
    Healthcare & Life Sciences
    HQ: United States