Site Contract Lead, FSP

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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

• Establish, maintain and update training material for the site contracts lead team and site contract negotiators • Serve as subject matter expert for global site contracting issues and escalation point for internal customers • Oversee clinical study agreement negotiations and drive document finalization and execution • Provide oversight of contract and budget negotiation status and manage escalations • Advise study teams and Sponsor stakeholders on industry trends, norms, risks and mitigation tactics • Act as first-line subject matter expert for CTA elements on assigned studies and advise on issue resolution • Plan contract execution strategy and forecast site-specific contractual execution timelines • Coordinate communications between study stakeholders and global site contract and budget negotiators • Prepare site contractual templates, payment terms, negotiation parameters and processes • Build working relationships with Sponsors and internal project teams • Identify contractual, budgetary and process risks and provide solutions • Create and maintain document status reports and update department tools, systems and team members • Collaborate with legal, finance and clinical operations departments • Manage discussions around fair market value of investigator budgets and payment terms • Identify best practices, investigate root causes and recommend solutions • Train and mentor less experienced staff on SOPs, processes, tools and templates • Support business units and the organization through help desk and other issue-resolution pathways • Lead internal training and process improvement initiatives as needed • Participate in business development presentations as a subject matter expert • Perform other work-related duties as assigned • Minimal travel may be required, up to 25%

🎯 Requirements

• BS degree or above • Legal background is a must • Strong experience in a CRO/pharmaceutical industry and related clinical trial expertise, 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, MS Project, Outlook and Internet • Ability to handle multiple tasks and meet deadlines in a dynamic environment • Above-average attention to detail • Effective oral and written communication skills • Ability to work independently to meet deadlines • Strong leadership skills • Ability to teach and mentor team members • Ability to coach employees to reach performance objectives • Strong background in issue resolution, meeting customer deliverables and driving best practices at organization or customer portfolio level • Equivalent experience, skills, and/or education will also be considered

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Total Self culture • Diversity and inclusive workplace • Comprehensive resources including emerging technologies, data, science and knowledge sharing • Multiple career paths and employment opportunities