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    Sr Global Feasibility Lead

    Syneos Health
    2+ years
    $72,540- 145,000
    Remote, USA
    10 Nov. 29, 2024
    Job Description
    Job Type: Full Time Education: BS/BA 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

    Senior Global Feasibility Lead

    Company: Syneos Health
    Location: Flexible, with potential travel requirements

    About Syneos Health

    Syneos Health is a leading biopharmaceutical solutions organization that drives customer success by accelerating the development and delivery of life-changing therapies. With a presence in 110 countries and a team of 29,000 employees, Syneos Health integrates clinical, medical, and commercial expertise to help address the evolving market needs.

    Why Syneos Health?

    • Career Growth: Opportunities for professional development and career progression in a dynamic and collaborative work environment.
    • Inclusive Culture: Syneos Health fosters a culture of diversity and inclusion, where all employees are encouraged to bring their authentic selves to work.
    • Global Impact: Join a team that works together to bring innovative solutions to the pharmaceutical and biopharmaceutical industries.

    Role Overview

    As a Senior Global Feasibility Lead, you will be responsible for managing and executing feasibility assessments across various therapeutic areas. You will work closely with internal stakeholders and clients, leveraging your expertise in clinical research to provide strategic guidance on site identification, recruitment support, and protocol feasibility.

    Key Responsibilities

    • Feasibility Assessments: Manage standalone paid feasibility assessments and RFPs (Requests for Proposal) for multiple projects across therapeutic areas.
    • Stakeholder Collaboration: Liaise with internal and external stakeholders, including Business Units, Medical Directors, and Business Development, to review sponsor requirements, protocols, and timelines for individual RFPs.
    • Research & Analysis: Conduct research using scientific literature, internal metrics, and tools to gather background information for feasibility assessments.
    • Data Management: Develop and maintain systems for the collection and analysis of historical feasibility data and metrics to support current RFPs.
    • Bid Defense: Support the preparation of materials for bid defense teleconferences and meetings.
    • Site Feasibility & Selection: Lead pre-award site-level feasibility assessments and deliver the findings in presentations or written reports to stakeholders.
    • Mentoring: Provide limited mentoring and guidance to junior team members, supporting their personal and professional development.
    • Technology Evaluation: Evaluate new technologies related to clinical trial registry search tools, enrollment modeling, and protocol feasibility tools.

    Qualifications

    Required Experience & Skills:

    • BS/BA in Science with a focus on medical research or a related field.
    • Experience: Ability to work independently and manage multiple assignments of varying complexity across any therapeutic area.
    • Research Skills: Knowledge of scientific research methodologies, clinical data analysis, and bid development.
    • Technology Proficiency: Strong skills in Microsoft Office Suite (Excel, Word, PowerPoint) and internet research tools.
    • Communication Skills: Excellent verbal and written communication skills in English, with the ability to present complex data clearly.
    • Attention to Detail: Strong organizational and attention-to-detail skills to ensure accuracy in feasibility assessments and reporting.
    • Team Collaboration: Ability to work effectively in a virtual team environment and collaborate across departments.

    Preferred Skills:

    • Mentorship: Experience in mentoring and training team members.
    • CRO Industry Knowledge: Familiarity with principles, concepts, and practices in the CRO (Contract Research Organization) industry.

    Compensation & Benefits

    Syneos Health offers a competitive salary based on experience, along with a comprehensive benefits package that includes:

    • Health, dental, and vision insurance.
    • 401(k) with company match.
    • Eligibility for Employee Stock Purchase Plan and performance-based commissions/bonuses.
    • Flexible paid time off (PTO) and sick leave.

    The annual base salary for this position ranges from USD $72,540 - $145,000 depending on qualifications and experience.

    Apply Now to join Syneos Health in shaping the future of global clinical trials and making a meaningful impact on patients' lives.

    Syneos Health is an equal opportunity employer, welcoming applicants from all backgrounds to apply.

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