Senior Site Contracts Manager - GSK - Oncology Focus - High Visibility

Morrisville, NC
Senior Site Contracts Manager - GSK – Oncology Focus - High Visibility

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.

Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Discover what our 29,000 employees, across 110 countries already know:

WORK HERE MATTERS EVERYWHERE

Why Syneos Health

  • We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
  • We are committed to our Total Self culture – where you can authentically be yourself. Our Total Self culture is what unites us globally, and we are dedicated to taking care of our people.
  • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives – we’re able to create a place where everyone feels like they belong.

Job Responsibilities

Minimum of 4 years experience

  • Develops and builds the US budget, site budget & language templates for Pharma & Vaccine studies.

  • Build US Site Budget Template

  • Provides expert guidance to develop detailed specifications and negotiate content of clinical trial agreements that are robust, timely, and add significant opportunity for value generation to the business while minimizing legal, operational, and financial risk during the contract life cycle.

  • Participates in creating and delivering solutions for simplifying work practices to increase productivity and reduce waste.

  • In the event the contracting party does not proceed forward with the initial offer the Contract Manager is responsible for performing due diligence checks which includes but is not limited to Fair Market Value and review of site justifications.

  • Determine if the contracting party’s requested changes warrant a budget and/or language escalation and to seek the appropriate approvals.

  • Escalate delays, impact to timelines, or risks that limit the ability to deliver a fully executed CTA within the timelines specified.

  • The Contract Manager should be very proficient in excel and other clinical trial management tools.

  • Demonstrate effectiveness in both oral and written communication. Effectively express ideas and incorporate feedback into deliverables to generate quality output.

  • Continuously development of knowledge of GCP, sponsor guidelines, SOPs, Work Instructions, Ways of Working, new technologies and capabilities.

  • The Contract Manager should have experience with clinical study protocols and study timelines and milestones (i.e. SIV).

  • Leads and supports diverse projects and initiatives as needed.

  • Effectively builds and maintains relationships with internal and external stakeholders.

  • Drives a culture of trust, respect, transparency, and accountability.

  • Timely and accurate updating of all departmental databases and trackers.

  • Ad hoc requests as needed.

  • Train and support additional team members as required.

Additional Preferred

  • Experience in oncology therapeutic area

  • Experience working in pharma and/or site

  • Project management skills

This is a US based remote position.

Salary Range

  • $79,800 – $139,600

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.

Salary Range:

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.

Get to know Syneos Health


Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

Additional Information


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. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Posted 2026-01-26

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