Site Contract Manager, II

🕒 August 11

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $47k - $95.9k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

👔 Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 13%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• Negotiate clinical trial budgets from start to finish directly with clinical sites from a Sponsor perspective • Understand budget and contract language for Pharma & Vaccine clinical trials • Develop and refine templates for consistency, compliance, and strategic study needs • Lead direct negotiations with large academic institutions and other critical stakeholders • Draft and finalize clinical trial agreements balancing business objectives with legal and operational protections • Conduct FMV assessments and site justification reviews when initial offers are declined • Determine when budget or language escalation is needed and secure appropriate approvals • Prioritize and lead multiple contracting projects across several therapeutic areas • Escalate risks, timeline impacts, or delays affecting CTA execution • Maintain accurate and timely updates in departmental trackers and databases • Build relationships with internal and external partners • Support and train additional team members • Contribute to process improvement initiatives • Take on ad-hoc tasks and diverse projects

🎯 Requirements

• 2+ years of experience in a fast-paced and volume-driven work environment • Direct experience negotiating with large academic institutions • Ability to juggle priorities, lead projects, and deliver results under tight timelines • Strong understanding of clinical study protocols, timelines, and site-related milestones, such as SIV • Bachelor’s degree • Expert proficiency in Excel and clinical trial management systems • Knowledge of GCP, sponsor processes, SOPs, and work instructions • Oncology therapeutic area experience preferred • Prior experience with pharma, CRO, or investigative sites preferred • Strong project management skills and comfort leading cross-functional efforts preferred • Experience leveraging AI in contracts and budgets preferred

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition and total rewards program • Inclusive culture • Company car or car allowance • Medical, Dental and Vision health benefits • Company match 401k • Eligibility to participate in Employee Stock Purchase Plan • Eligibility to earn commissions/bonus based on company and individual performance • Flexible paid time off (PTO) • Sick time • Reasonable accommodations, when appropriate • Comprehensive resources including emerging technologies, data, science and knowledge sharing