Site Contracts Specialist with experience in Clinical Trials, Home-Based Mexico, Brazil and Arg[...]

Site Contracts Specialist 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 we do. We are continuously looking for ways to simplify and streamline our work to make Syneos Health easier to work with and 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. Job Responsibilities May lead multi‑country projects, including negotiating and preparing contracts, budgets, and related documents for participation in industry‑sponsored clinical trials. Produces site‑specific contracts from country clinical trial agreement (CTA) template and reviews/owns site‑specific contracts from country template. Submits proposed CTA and investigator budget for site review. Negotiates budget and contract with site and via Site Contracts Service Centre and SSUL with Sponsor until resolution of issues. Performs quality control and arranges execution of CTAs as well as archival of documents into repositories and capture of metadata; reviews contracts for completeness and accuracy. Administers all contract management processes, coordinating with relevant protocol, informed consent, institution, investigator, vendor, consultant, and customer agreement documents at a project level. Generates amended contract and/or budget documents as necessary, preparing contract‑management documentation for projects and streamlining the contract/proposal or internal processes; initiates and introduces creative ideas and solutions. Works closely with Site Contract Service Center and Legal to harmonize site contract to reflect sponsor's master service agreement terms. Works closely with SSU lead, Clinical Operations and Finance to validate the load of departmental budgets and corresponding backlog. Identifies possible contract or process operational risk and proactively works within the team to provide solutions. Establishes strong working relationships with SSU lead, customer and internal project teams; escalates deviations to department leadership and/or Site Contract Service Center and/or Legal Department. Provides support to business development and represents site contracts/Site Start‑Up (SSU) at internal or customer meetings. Works within the forecasted country/site contracting timelines, ensures compliance, and tracks milestone progress in agreed‑upon SSU tracking system in real time. Collaborates with internal and external legal, finance, and clinical operations departments, including communicating and explaining legal and budgetary issues. Maintains and actively supports review and development of contract templates, budget templates and site‑specific files and databases. Serves as key communication liaison between site contracts staff and internal and external customers; provides functional guidance and keeps teams aware of all contract statuses or pending issues. Trains and mentors less experienced staff members on departmental Standard Operating Procedures (SOPs) and ensures quality of team work products. Actively participates in higher‑level discussions about overall company goals, departmental objectives, and specific project aims. Facilitates the execution of contracts by company signatories. Monitors basic financial aspects of the project and the number of hours/tasks available per contract; escalates discrepancies in a timely fashion. Reviews and complies with SOPs and Work Instructions (WIs) in a timely manner, keeps training records updated and ensures timesheet compliance. Qualifications BA/BS degree in Business Administration, Public Administration, Public Health, or related field (advanced degree preferred). Moderate contract management experience, including experience in a contract research organization or pharmaceutical industry. Management experience preferred. Strong knowledge of the clinical development process and legal and contracting parameters. Strong computer skills in Microsoft Office Suite. Customer‑focused and able to manage challenging priorities while remaining flexible and adaptable in stressful situations. Excellent understanding of clinical trial process across Phases II‑IV and ICH GCP. Good understanding of clinical protocols and associated study specifications. Excellent understanding of clinical trial start‑up processes. Project management experience in a fast‑paced environment. Vendor‑management skills and strong organizational skills with proven ability to handle multiple projects. Excellent communication, presentation and interpersonal skills. Quality‑driven in all managed activities. Strong negotiating and problem‑solving skills. Ability to mentor and motivate more junior staff and provide quality feedback and guidance to peers. Contribute to a training and quality‑assurance plan within SSU and update SOPs/WI. Salary range: $56,000 – $95,000 (actual salary will vary based on qualifications and other factors). Location This is a remote/home‑based position open to candidates located anywhere within the United States. Additional Information Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications may differ from those listed. The Company will determine what constitutes as equivalent to the qualifications described here. Nothing herein should be construed to create an employment contract. The Company is committed to compliance with the Americans with Disabilities Act and provides reasonable accommodations when appropriate. #J-18808-Ljbffr