Role Description Site Contracts Specialist with clinical trials experience Home-Based in Argentina. - 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. Reviews and 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, and ensures that corrections are appropriately made and documented. - Administers all contract management processes, including coordination 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 they are complied with 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 internal and external teams aware of all contract statuses or pending issues. Prepares correspondence as necessary. - Trains and mentors less experienced staff members on departmental Standard Operating Procedures (SOPs), and ensures quality of team work products. Maintains and updates training material for site contract team. - 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 Standard Operating Procedures (SOPs) and Work Instructions (WIs) in a timely manner, keeps training records updated accordingly and ensures timesheet compliance. Qualifications - BA/BS degree in Business Administration, Public Administration, Public Health, related field, or equivalent combination of education and experience. Advanced degree preferred. - Moderate contracts management experience that includes 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 ability to manage challenging priorities and to remain flexible and adaptable in stressful situations. - Excellent understanding of clinical trial process across Phases II-IV and ICH GCP. - Good understanding clinical protocols and associated study specifications. - Excellent understanding of clinical trial start-up processes. - Project management experience in a fast-paced environment. - Good vendor management skills. - Strong organizational skills with proven ability to handle multiple projects. - Excellent communication, presentation and interpersonal skills. - Quality-driven in all managed activities. - Strong negotiating skills. - Strong problem-solving skills. - Ability to mentor and motivate more junior staff. - Demonstrate an ability to provide quality feedback and guidance to peers. - Contribute to a training and Quality assurance plan within SSU and update SOPs/WI. Benefits - 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 building an inclusive culture – where you can authentically be yourself. - We are continuously building the company we all want to work for and our customers want to work with. Company Description Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

• Develop and expand long-term customer relationships • Actively identify and acquire new B2B customers in Eastern Austria, Slovenia, Croatia, and Hungary • Plan, implement, and achieve the regional sales budget • Manage and close sales projects • Prepare quotations and follow up on offers • Conduct customer loss analyses and develop win-back strategies • Ensure customer satisfaction through professional handling of feedback and complaints • Prepare sales reports and analyses to guide sales activities • Represent the company at trade fairs and industry events

• Develop and expand long-term customer relationships • Actively identify and acquire new B2B customers within Eastern Austria, Slovenia, Croatia, and Hungary • Plan, implement, and achieve the regional sales budget • Manage and close sales projects • Conduct customer loss analyses • Ensure customer satisfaction through professional handling of feedback and complaints

Role Description Site Contracting is an essential function within any CRO, and our seasoned team spans decades of experience within the industry and possesses robust legal experience as well. The department is responsible for reviewing, analyzing, and drafting clinical research site contracts, investigator contracts, and other project-related contracts. Our global team is familiar with the specific laws for the countries and sites we occupy. We negotiate and finalize clinical trial contracts and services contracts with the Worldwide Legal Department, study teams, Sponsors, investigators, and/or clinical sites. - Prepare country contract templates; - Draft and send Site Agreements or any contracts associated to sites to begin negotiations; - Negotiate contract(s) language and budget(s) with each assigned site to finalization/execution; - Review study budgets and costs pertaining to contract negotiation; - Perform quality check of Site Agreements or any documents associated before signature process starts; - Liaise with Worldwide Legal Department, Data Privacy team, study teams, Sponsor, sites, investigators, etc.; - Send Fully Executed Site Agreements or any document associated to: site, eTMF, payment team, Sponsor, post to internal Sharepoint, as applicable; - Negotiate Site Agreements Amendment language and budget with sites; - Create termination letter or any other type of documents related, and send to sites for signature, as applicable; - Maintain tracking tool with live/real-time/regular updates for functional activities; Qualifications - Bachelor's Degree or equivalent in business administration, finance, science or related field. - 1 to 3 years of experience in Clinical Research Pharmaceutical or CRO industry working with investigator/site contracts or related legal field. - Excellent verbal and written English, along with proficiency in either Spanish, French, Polish, or German. - Proficiency with MS Word, Excel and Outlook. Requirements - Proficient in negotiating contract terms with clinical sites and vendors. - Ability to identify and address contract issues and disputes efficiently. - Good understanding of international and local regulatory requirements for clinical trials (e.g., FDA, EMA, ICH-GCP). - Solid analytical skills to review and interpret contract terms and financial data. - Ability to identify risks and develop mitigation strategies. Benefits - We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.