Site Contracts Lead

🔥 40 minutes ago

🌐 China, Taiwan – Remote

🇨🇳 China – Remote 🇹🇼 Taiwan – Remote

⏰ Full Time

🟠 Senior

👻 Ghost score 10%

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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

• Oversee negotiations of clinical study agreements at study level • Drive CTA document finalization and execution, including contractual language and terms, financial attachments, and investigator grant budgets • Provide oversight of contract and budget negotiation status • Manage escalation of out-of-parameter budgetary and contractual queries to sponsor decision-makers • Act as first-line subject matter expert for CTA elements on assigned studies • Advise stakeholders on issue resolution • Plan contract execution strategy and forecast site-specific contractual execution timelines • Coordinate with internal study team stakeholders to align CTA strategy with study start-up plans • Manage expectations regarding global CTA negotiations • Coordinate communications between study stakeholders and global site contract and budget negotiators • Participate in regular study calls • Prepare site contractual templates, payment terms, study-level negotiation parameters and processes • Establish working relationships with Sponsors to align contractual templates with global program strategy • Create and maintain document status reports and update department tools, systems and team members • Collaborate with legal, finance and clinical operations departments • Manage discussions regarding fair market value of investigator budgets and payment terms • Support business units and the organization through help desk and other defined pathways • Perform other work-related duties as assigned

🎯 Requirements

• BS degree in life sciences, a health related field, or equivalent combination of education and experience • Preferred 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 • Good presentation, documentation and interpersonal skills • Proficient in MS Office (Word, Excel and PowerPoint), MS Project, Outlook and Internet • Ability to handle multiple tasks to meet deadlines and deliver high quality work in a dynamic environment • Attention to detail • Effective oral/written communication skills • Ability to work independently to meet deadlines • Strong leadership skills • Ability to teach/mentor team members

🏖️ Benefits

• Career development and progression • Supportive and engaged line management • Technical and therapeutic area training • Peer recognition • Total rewards program • Inclusive culture • Minimal travel may be required (up to 25%)

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