<div><b>Description</b><br/> Senior Site Contracts Manager (Sponsor Dedicated /Remote - US Based)<br/><br/><b>Job Responsibilities</b><br/><br/><b>Senior Site Contracts Manager (Sponsor-Dedicated /Remote - US Based)</b><br/><br/>Are you a contracts expert who thrives on navigating complexity, building strong site partnerships, and driving timelines forward? Syneos Health is seeking a <b>Senior Site Contracts Manager</b> to support a sponsor-dedicated program focused on high-impact Pharma & Vaccine studies. If you're energized by problem-solving, negotiation, and leading projects across multiple therapeutic areas-especially oncology-we'd love to meet you.<br/><br/><b> About the Role: </b><br/><br/>As a <b>Senior Site Contracts Manager</b>, you'll serve as a strategic expert responsible for negotiating and managing US site budgets and clinical trial agreements (CTAs). You'll collaborate closely with internal teams, external stakeholders, and major academic institutions to craft robust contracts that support operational excellence while minimizing risk.<br/><br/>This role is perfect for a communicator, leader, and negotiator who's ready to hit the ground running and make an immediate impact.<br/><br/><b> Key Responsibilities: </b><br/><br/><b>Budgeting & Template Development</b><br/><ul><li>Create US templates and study-specific budget language for Pharma & Vaccine clinical trials.</li><li>Develop and refine templates to support consistency, compliance, and strategic study needs.</li></ul><br/><br/><b>Contract Negotiation & Risk Management</b><br/><ul><li>Lead direct negotiations with <b>large academic institutions</b> and other critical stakeholders.</li><li>Draft and finalize clinical trial agreements that balance business objectives with legal and operational protections.</li><li>Conduct due diligence checks-such as FMV assessments and site justification reviews-when initial offers are declined.</li><li>Determine when requests require budget or language escalation and secure appropriate approvals.</li></ul><br/><br/><b>Project Leadership & Delivery</b><br/><ul><li>Prioritize and lead multiple contracting projects across several therapeutic areas (oncology experience strongly preferred).</li><li>Proactively escalate risks, timeline impacts, or delays that could affect CTA execution.</li></ul><br/><br/><b>Tools, Systems & Communication</b><br/><ul><li>Demonstrate expert proficiency in <b>Excel</b> and clinical trial management systems.</li><li>Communicate effectively in both written and verbal formats, incorporating feedback seamlessly.</li><li>Maintain accurate and timely updates in departmental trackers and databases.</li></ul><br/><br/><b>Compliance, Collaboration & Continuous Improvement</b><br/><ul><li>Deepen and maintain knowledge of GCP, sponsor processes, SOPs, work instructions, and new technologies.</li><li>Build strong working relationships with internal and external partners.</li><li>Support and train additional team members as needed.</li><li>Contribute to process improvement initiatives that simplify workflows and eliminate inefficiencies.</li><li>Take on ad-hoc tasks and diverse projects with a solutions-oriented mindset.</li></ul><br/><br/><b> What You Bring (Minimum qualifications): </b><br/><ul><li><b>4+ years</b> creating US contracts from templates</li><li>Direct experience negotiating budgets and contracts with large academic institutions</li><li>Ability to juggle priorities, lead projects, and deliver results under tight timelines</li><li>Strong understanding of clinical study protocols, timelines, and site-related milestones (e.g., SIV)</li><li>Bachelors degree</li></ul><br/><br/><b> Preferred Qualifications: </b><br/><ul><li>7+ years of experience in clinical site contracting, including significant experience leading US budget and CTA negotiations</li><li>Demonstrated experience supporting oncology clinical trials, with additional exposure to respiratory or vaccine studies strongly preferred</li><li>Prior experience working within a sponsor-dedicated model or directly for a pharmaceutical or biotech company</li><li>Advanced project management capabilities, including leading cross-functional initiatives and influencing stakeholders to meet aggressive timelines</li><li><b>Oncology & Respiratory therapeutic area experience</b></li><li>Prior experience with <b>pharma</b></li><li>Strong <b>project management</b> skills and comfort leading cross-functional efforts</li></ul><br/><br/>If you're ready to elevate your contracting career in a critical sponsor-dedicated role-and join a team driven by trust, transparency, and high performance-this is your opportunity!<br/><br/><b>Salary Range</b><br/><ul><li><b>$79,800 - $139,600</b></li></ul><br/><br/>At Syneos Health, we believe in providing an environment and culture in which Our People can thrive, develop and advance. We reward and recognize our people by providing valuable benefits and a quality-of-life balance. The benefits for this position may include a company car or car allowance, Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock Purchase Plan, Eligibility to earn commissions/bonus based on company and individual performance, and flexible paid time off (PTO) and sick time. Because certain states and municipalities have regulated paid sick time requirements, eligibility for paid sick time may vary depending on where you work. Syneos complies with all applicable federal, state, and municipal paid sick time requirements.<br/><br/>Salary Range:<br/><br/>The base salary range represents the anticipated low and high of the Syneos Health range for this position. Actual salary will vary based on various factors such as the candidate's qualifications, skills, competencies, and proficiency for the role. <br/><br/><b>Additional Information</b><br/><br/>Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.<br/><br/><b>Summary</b> <br/> In need of a Senior Site Contracts Manager. Candidates must have at least 4 years of building contracts from templates and negotiating both budgets and contracts directly with large academic institutions from a Sponsor perspective. Candidates must have ability to prioritize and lead projects and have experience in multiple TAs - preferably oncology & respiratory. Candidates must be able to start ASAP. This is a US based remote position.</div>
