Senior Contracts Associate

Beigene

Alcobendas

Presencial

EUR 58.000 - 72.000

Jornada completa

Hace 6 días
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Descripción de la vacante

BeOne is seeking a Senior Contract Associate in Spain to draft, negotiate, and finalize complex Clinical Site Contracts for our clinical trials, ensuring timely data entry into CMS and related systems.

You will coordinate with Global Clinical Operations, Legal, Investigator Sites, and external providers to meet deadlines while upholding BeOne policies and regulatory requirements. Prior experience in pharma contract management is preferred.

Responsabilidades

  • Prepare, negotiate, and finalize clinical trial agreements with sites.
  • Manage budget grid in the contract; ensure cost calculations align with protocol.
  • Execute contracts on time and within targets across the trial lifecycle.
  • Coordinate with Legal, GCO, IPM, investigator sites and external providers.
  • Maintain CMS records and real-time trackers; perform quality checks on final documents.

Descripción del empleo

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description:

The Senior Contract Associate is responsible for drafting, negotiating, and finalizing complex Clinical Site Contracts related to clinical trials throughout the lifecycle of the study, and performs timely and accurate data entry into all Clinical Business Operations operating systems, including but not limited to the company Contract Management System (CMS). The Contract Associate is also responsible for meeting deliverables with high quality and within the project timelines. The contracting activity supported by the CBO team is fast-paced, with short deadlines and quick turnaround times therefore Contract Associate must be capable of managing priorities effectively, proactively communicating issues and working in a fast-paced environment.

Essential Functions of the job:
  • Prepare, negotiate, and finalize clinical trial agreements, ancillary agreements and amendments of company sponsored studies through direct communication with sites.
  • Responsible for execution of contracts against planned timelines and targets.
  • Manage budget grid in the contract. Ensure the cost calculation are consistent with protocol and agreed with site.
  • Demonstrates an understanding of records management requirements for contract documents
  • Complete quality check (QC) of final approved contract and budget documents, and initiates signature process of assigned contracts to the responsible signing parties.
  • Ensure final contracts are delivered to agreed timelines, within Fair Market Value & in compliance with relevant legal and regulatory requirements
  • Serve as the primary point of contact between CBO and Global Clinical Operations (GCO), Legal, Investigator Sites and external service providers in accordance with the study related activities to meet business needs;
  • Collect and maintain country and site intelligence information for each country and/or site, and prepares country/site specific contract process flows as needed;
  • Forecast, set, track and communicate fully executed contract planned dates, and make all efforts to achieve the set planned date, ensuring the CM and study teams are proactively informed of changes and/or risks to the projected dates;
  • Liaise with CM and BeOne legal to review and update contract template(s) as needed, including Master Clinical Trial Agreements/Clinical Trial Agreements/Project Agreements or any other Site agreement template(s);
  • Liaise with CM and BeOne legal to contribute updates to the BeOne Legal Playbook guidance document as needed;
  • Liaise with Investigator Payment Management (IPM) team to ensure site contracts, including investigator site budgets, are approved and executed in accordance with CBO guidelines and BeOne policies;
  • Ensure all investigator contracts are reviewed and approved by legal and/or delegate prior to execution, and in accordance with CBO and BeOne legal guidelines;
  • Communicate legal and budgetary issues to internal and external parties per department guidelines, as needed;
  • Perform legal translation of contract language for Sites, as needed;
  • Maintain active and regular communication with site personnel and internal BeOne partners, with regular progress tracking and updates provided throughout the contract lifecycle;
  • Prepare subsequent contract amendments, note to files and other related contract documents, as needed;
  • Escalates contracting issues and/or potential delays to internal and external stakeholders, as necessary;
  • Attend and actively participate in Investigator Site, project related, CBO, and other meetings, as necessary;
  • Update and maintain CBO trackers with real-time updates on a regular basis, complete CBO related filing and distribution of contract documents, and maintain Contract Management System (CMS) records, in accordance with CBO and BeOne policies;
  • Provides a handoff to the project/payment

Salary Range Spain: 57,600.00 EUR - 72,000.00 EUR

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity
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