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Contract & Budget Specialist

Work mode:  Hybrid
Onsite Location(s): 

Hemel Hempstead, HRT, GB

Additional Locations: United Kingdom-Hemel Hempstead

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

 

 

About the role

As a part of Boston Scientific's Global Clinical Contract Operations, you will develop, negotiate, and finalize Clinical Site Agreements and Budgets for medical device clinical trials in a variety of therapeutic areas by collaborating with internal key stakeholders and working with external health care institution staff. This role is a key element on the study start-up process to allow sites to participate on Boston Scientific’s Clinical Studies and ensure study enrollment.  

 

 

Your responsibilities will include:

 

  • Preparation, negotiation, analysis, escalation, and finalization of all site agreements and budgets.
    • Customizes Agreement and Budget Templates: Leverages historical site data to tailor the agreement and budget templates specifically for each site, ensuring relevance and accuracy.
    • Coordinates with Site for Contract Execution: Engages with site representatives to align on expectations and timelines for contract execution, aiming to meet the targeted authorization date efficiently.
    • Conducts Budget Analysis and Negotiation: Reviews and analyzes the proposed budget against Fair Market Value (FMV) parameters. Utilizes historical data to negotiate site requests, ensuring consistency and fairness across site and study budgets.

 

  • Accelerate negotiations by using budget parameters.
    • Negotiates Site Budgets: Utilizes the fair market value established at the study’s inception to negotiate budgets with sites, ensuring financial alignment and transparency.
    • Reviews and Analyzes Costs: Examines requested costs to determine their applicability to the specific phase and indication of the trial, ensuring budgetary compliance and relevance.
    • Escalates Unresolved Fees: Escalates any fees that sites refuse to decrease or waive, gathering all necessary cost justifications to present to the Fair Market Value team for further review.
    • Engages in Site Discussions: Participates in calls with site representatives to gain a deeper understanding of their requests, fostering clear communication and effective negotiation.

 

  • Working with legal stakeholders to negotiate contracts.
    • Collaborates with BSC Legal Team: Works closely with the BSC legal department to negotiate and establish mutually agreeable terms between the institution and the sponsor, ensuring all parties’ interests are adequately represented.
    • Drafts and Finalizes Amendments: Develops necessary amendments for ongoing trials, coordinating with the legal team to finalize these documents for site execution during the maintenance phase, ensuring compliance and smooth operation.
    • Manages Contract Concerns: Addresses and resolves contract-related issues by liaising with various divisions, effectively navigating potential standoffs and facilitating successful contract negotiations.

 

  • Maintain regular communication and escalation to expedite the planning, execution, issue resolution, and management of Site/Investigator agreements.
    • Communicates Site Concerns with Trial Managers: Engages in discussions with trial managers to address and resolve any concerns raised by sites, ensuring smooth and effective trial operations.
    • Highlights Contract and Budget Issues: Proactively brings any contract and budget-related concerns to the attention of trial managers as they arise during the study, facilitating timely resolution and maintaining financial integrity.
    • Monitors and Supports Site Performance: Identifies sites that are not meeting established timelines and coordinates calls with the trial team to set clear goals and strategies for getting the site back on track, ensuring adherence to project schedules.

 

  • Understand Site Activation requirements versus contracting turnaround times to support study site authorization.
    • Coordinates with TCRAs for Contract Timelines: Works closely with TCRAs to establish a timeline for contract execution, facilitating the planning of site authorization and enabling timely patient enrollment in critical trials.
    • Routinely Reassesses Timelines with Study Team: Regularly checks in with the study team throughout the study start-up phase to reassess contract and budget timelines, identifying and navigating potential barriers to ensure adherence to target dates.

 

 

What are we looking for in you:

 

  • Bachelor’s degree, or equivalent experience.
  • Minimum of 5 years Industry experience managing clinical site contracts & budgets.
  • Demonstrates effective time management skills, including the ability to prioritize multiple tasks independently.
    • This ensures that all aspects of the negotiation process are handled promptly and deadlines are consistently met.
  • Demonstrates the ability to work independently and take initiative to prevent and resolve issues
    • This includes anticipating potential challenges and implementing solutions without needing constant supervision.
  • Demonstrates the ability to have strong analytical and organizational skills.
    • Strong organizational skills are essential for managing various documents, tracking progress, and maintaining detailed records throughout the negotiation process.
  • Demonstrates the ability to communicate effectively in English, both in writing and orally.
    • This includes drafting precise contract language, articulating budgetary concerns, and negotiating terms with clarity and professionalism.
  • Demonstrates interpersonal skills demonstrated by being proactive, customer-focused, and independent critical thinker.
    • This involves understanding the needs and concerns of all parties involved, fostering positive relationships, and thinking strategically to achieve mutually beneficial outcomes.

 

 

As a Disability Confident employer, we welcome applications from all backgrounds and are committed to providing reasonable adjustments to support candidates and employees with disabilities.

 

 

 

Requisition ID: 635009

 

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn.


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