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Syneos HealthVerified from Syneos Health's careers page · Workday

Sr. Site Grant Analyst/Grant Analyst II (Serbia) hybrid, sponsor dedicated

  • Srb-Belgrade-Hybrid
  • 5 Years
  • Posted Nov 3, 2026

At a glance

Sr. Site Grant Analyst/Grant Analyst II (Serbia) hybrid, sponsor dedicated at Syneos Health, based in Srb-Belgrade-Hybrid. Experience level: 5 Years. Posted on 3 November 2026, read from Syneos Health's own careers page (Workday), which RealAnalystJobs re-checks daily and removes the role when it closes.

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About this role

Sr. Site Grant Analyst/Grant Analyst II (Serbia) hybrid, sponsor dedicated 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. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. 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 deliver – for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know: 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 building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress. Job Responsibilities Core Responsibilities Establishes, maintains and updates training material for investigator budget team and site contract negotiators. Serves as subject matter expert equipped to help resolve global site budgeting issues, and escalation point within the Company for internal customers to seek assistance. Proposes site budgeting solutions to issues that may arise during a project or contract/budget life cycle to enhance negotiation strategy and ensure deliverables are met. Establishes project strategies around investigator budget template development and/or budget negotiation parameters to reflect sponsor's specifications, communications and required processes. Initiates and introduces creative ideas and solutions. Develops detailed investigator grant budget estimates and country budget templates according to protocol specifications through currently available software package/resources. Updates detailed investigator grant budget estimates and country budget templates according to protocol amendment specifications through currently available software package/resources. Works closely with internal stakeholders to draft, collaborate with Sponsor and harmonize investigator budget templates, investigator budget parameters and payment terms within Company processes. Ensures investigator budget templates are drafted and updated taking into consideration fair market value and key operational aspects indicated in the relevant operational documents (e.g. protocol, Integrated Site Activation and Maintenance Plan, etc.), as well as in the customer agreement documents at a project and organizational level. Establishes strong working relationships and collaboration with Sponsor to ensure site budget templates fit into the global strategy set for the program. Validates investigator grant budget estimates against available internal and external benchmarking data. Identifies possible investigator budget or process operational risk and works to provide solutions. Establishes strong working relationships with customer and internal project teams. Escalates deviations to senior management and is equipped to resolve issues with Quality Assurance. Creates and maintains document status reports, and updates department tools/systems and team members on a regular basis; ensures appropriate documentation is maintained. Collaborates with internal and external legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues. Researches, compiles and creates necessary information as required in support of obtaining fair market value and developing investigator budget templates. Identifies best practices, investigates root causes of fundamental issues and problems for projects and recommends solutions. Recognizes and develops opportunities for continuous process improvement within investigator budget template development, which lead to greater efficiencies and/or leading best practices. Trains and mentors less experienced staff members on department Standard Operating Procedures (SOPs), processes, tools and templates and ensures quality of teamwork products. May support BU and organization through help desk and other defined pathways to resolve and deescalate issues. May identify and lead internal team training and/or process improvement initiatives. Participates in business development presentations as a subject matter expert in budget development and Fair Market Value (FMV) within the Company. Performs other work-related duties as assigned. Minimal travel may be required (up to 25%). Qualifications Education Requirements Min/Preferred Education Level Description BS degree in life sciences, a health related field, or equivalent combination of education and experience. Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise (Study Coordinator, CRA, Pharmacy, Nursing, Healthcare Administration) or site start-up experience. Thorough knowledge of applicable regulations, drug development and clinical project management procedures. Strong presentation, documentation and interpersonal skills. Proficient in MS Office (Word, E

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