
Clinical Trial Manager
Posted 1 day ago

Posted 1 day ago
This is a fully remote position, open to applicants in Connecticut.
• Ensure that the budgets for clinical trials and sites are of high quality and that allocations align with fair market values.
• Develop and sustain the Sites Fee Framework.
• Coordinate, process, oversee, and manage site payments in accordance with budgets and stipulated terms.
• Prepare, negotiate, and finalize agreements.
• Review contract language and draft responses to negotiate modifications to contracts.
• Maintain organized contract files and systems.
• Construct clinical trial site budgets and analyze protocol flowcharts to devise costing, payment strategies, budget estimates, and negotiation parameters that comply with fair market value.
• Set up, close, re-open, and submit payments related to grants.
• Utilize budget-specific and trial metrics and tools to report on, provide visibility into, and analyze performance and deliverables.
• Identify and implement continuous improvement strategies to enhance operational effectiveness.
• Stay updated with industry standards, trends, competitive intelligence, and best practices related to budgets.
• Collaborate with Medical, therapeutic areas, Finance, Legal, investigators, site personnel, and third-party vendors.
• Communicate with Clinical Trial Managers and TA Leads for budget review and approval.
• Work in conjunction with Clinical Finance/Accounting, Legal, and Clinical Operations leadership on decisions and documentation related to payments.
• Represent the Contract/Budget group processes in local and global working groups.
• Maintain a customer-centric approach and responsiveness to both internal and external requests.
• Bachelor's degree.
• At least five (5) years of pertinent business experience in the regulated pharmaceuticals or healthcare sector.
• Strong clinical background with an understanding of cost drivers and benchmarks for clinical site budgets.
• Ability to think strategically and formulate strong, persuasive contractual arguments to support business policies and objectives.
• Proven track record in prioritization, organization, and problem-solving skills that foster sound decision-making.
• Excellent customer service abilities and meticulous attention to detail.
• Demonstrated analytical and critical thinking skills to resolve complex issues that require innovative solutions.
• Outstanding written and verbal communication skills, with the ability to convey information clearly and concisely across varied communication settings.
• Experience with systems and applications related to clinical and/or project management planning and reporting.
• Proficient in Excel, Word, and Access.
• Familiarity with Veeva is a plus.
• 12 Months Contract
Thermo Fisher Scientific
Fortrea
Fortrea
Worldwide Clinical Trials
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