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Are you ready to make your mark in the healthcare industry using your ingenuity and technical expertise? At Parexel, there's no limit to what you can accomplish. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. With a role in our Information Technology group, you'll work with cutting-edge technology on internal and client-facing projects. Collaborating with people from all over the world and touching everything from enterprise systems and clinical applications to infrastructure and networking, you'll keep our data safe and confidential. You'll have the chance to develop your skills and pursue advancement opportunities that include managerial and technical tracks. If you have stellar coding and design experience and a passion to learn more about healthcare, Parexel invites you to discover our rewarding opportunities in Enterprise Architecture, Software Development, Project Management and Business Analysis, and more. In a global clinical trial environment, business-focused applications, connectivity, and data security are critical to a trial's outcome. Find out how you can be an invaluable part of our success story.

Manager, Clinical Site Contracts and Budgets - Spain - FSP

Job ID R0000044238 , Spain

At Parexel FSP, people make a difference. We have a key mission: to prevent and treat disease by bringing important new medicines and therapies to patients in need. We achieve this important goal through the expertise, experience, innovation, and commitment of our employees around the world.


Our employees have the opportunity to do meaningful things around the world, while we support them locally in environments of challenge, collaboration, flexibility and industry-leading growth potential.


Parexel FSP is looking for a SiteContracts Lead in Spain, 100% remote. 

A single sponsor dedicated.


In this position, you will be responsible for drafting, negotiating, and implementing global investigative site budgets and contracts for assigned studies, including reviewing sites’ proposed changes/requests, to ensure the timely and compliant delivery of site clinical trial agreements while developing and maintaining positive relationships with sponsor´s investigative sites.The role will involve collaborating with stakeholders internally as well as with external partners.


Expect exciting professional challenges, but with a healthy work-life balance. Your wellbeing is as important to us as our patients.


For each role, we look for professionals who have the determination and courage to always put the patient's wellbeing first. For us, this is a job with heart.


Some details of the role:

  • Serve as the site contracts and budgets lead across assigned studies accountable for ensuring the timely, high quality and compliant execution of the site budget and contract negotiation process
  • Collaborate with key stakeholders on the study team from early planning and throughout the contract lifecycle to prioritize, plan and execute in alignment with operational objectives
  • Actively and regularly drive prioritization and progress on site contracts within the clinical trial working group
  • Develop or oversee budget setup including study-specific parameters for assigned studies using industry tools and data sources
  • Manage site contracting related issues efficiently and according to escalation pathways
  • Communicate effectively internally and with external partners to ensure alignment and excellence in coordination of study start-up activities (i.e. SIV scheduling)
  • Ensure that all relevant systems and trackers are accurate and timely with regard to the disposition of site budgets and contracts
  • Apply standards to the site budgeting and contracting process across studies/programs
  • Manage all changes to study scope ensuring timely implementation of amendments.
  • Lead site budget and contract process improvement initiatives, as required
  • Manage against study-level KPIs and metrics for site budget and contract negotiation
  • Train and mentor peers and stakeholders, as required.
  • Partner with Legal, Compliance and other collaborating functions on continuous improvement to site budgeting and contracting processes.
  • Complies with required training curriculum
  • Completes timesheets accurately as required
  • Submits expense reports as required
  • Updates CV as required
  • Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements

Experience required for this role:

  • At least 5 years of experience with leading clinical budgets and contracts negotiation.

  • Fluent in Spanish and English is a must.

  • Skills:

  • Strong relationship building, negotiation, and conflict resolution skills
  • Demonstrated excellent verbal, written, and interpersonal communication skills
  • Demonstrated understanding of clinical operations and study start-up
  • Demonstrated experience with driving global site budget and contract strategies
  • Familiar with common budget development and data tools (e.g. Grant Plan)
  • Demonstrated understanding of regulatory and legal issues related to the conduct of clinical trials
  • Education:
  • A bachelor’s degree is required
  • JD or MBA preferred

We will offer you

  • Premium salary.

  • Attractive benefits.

  • Medical care plan: Health, Dental & Vision.

  • Life Assurance.

  • Excellent work environment.

  • Culture of teamwork and collaboration.

  • People who motivate and face challenges together.

  • Innovative technology.

  • Excellent training.

For more information, please contact marta.kuniewicz@parexel.com


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