
Senior Director, Scientific Affairs
Posted Oct 6

Posted Oct 6
This is a fully remote position, open to applicants in United States.
• Drive and support operational aspects related to RFPs and bid defense meetings.
• Manage global relationships with third-party laboratories.
• Represent Precision lab operations during pre-award, internal, and external kick-off meetings.
• Lead projects that foster innovation and competitive advantages.
• Collaborate with teams across scientific, operational, business development, proposal, and functional leadership.
• Hire, train, develop, and mentor direct reports.
• Own, maintain, and report on staff and department metrics.
• Develop operational specifications based on client protocols, including aspects like enrollment, feasibility, study timelines, and startup timelines.
• Interpret protocols and assay specifications for global laboratories.
• Attend post-award monthly and governance meetings; gather metrics and reconcile invoicing and billing.
• Create specification sheets and acquire quote information.
• Develop and review proposal text, including quotes from third-party labs.
• Ensure that proposals align with strategic, operational, scientific, and clinical development plans.
• Support the budget development for study proposals related to both internal laboratories and third-party lab partners.
• Transition operational strategies to lab operations in preparation for internal kick-off meetings.
• Participate in post-award meetings to facilitate study execution.
• Mentor and train colleagues in scientific affairs and Precision.
• Assist in capabilities presentations and pre-award client meetings.
• Provide insights on feasibility and scientific landscapes for bid defense meetings.
• Collaborate on innovative solutions for clients.
• Support the post-award delivery of data and milestones.
• Represent the company at industry events, speaking engagements, and booth exhibitions.
• Publish articles related to scientific or industry topics.
• Bachelor's degree in a life sciences discipline or equivalent relevant experience.
• Advanced degree, PhD preferred.
• 15+ years of experience in the CRO/Lab industry or equivalent relevant experience and/or demonstrated competencies.
• Proven experience in leading and influencing a global laboratory network, including oversight of multi-site laboratory operations.
• Experience in establishing standardized processes and quality systems.
• Familiarity with aligning regional laboratories to enterprise-wide strategic, operational, and compliance objectives.
• Experience in operational protocol analysis and budget review.
• Strong background in Precision’s target therapeutic area clinical development, focusing on operational delivery, strategy, feasibility, budget development, and execution of all phases of clinical trials.
• Management or oversight experience with third-party lab partners.
• Candidates must be legally authorized to work in the country of employment without requiring employer sponsorship.
• Discretionary annual bonus.
• Health insurance.
• Retirement savings benefits.
• Life insurance.
• Disability benefits.
• Parental leave.
• Paid time off for sick leave and vacation.
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