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Senior Contracts Associate

Remote from Spain·Full-time·Added 8 days ago (last checked 15 Oct)

Overview

Salary
€57,600 - €72,000 a year

About €3,340 - €4,050 a month after tax, or €3,340 - €4,240 under the Beckham regime.

Work mode
Remote from Spain
Contract
Permanent contract, full-time hours
English
Required

Visa options

  • The ad doesn’t mention sponsorship

    Not a refusal, but not a yes. Worth asking in your first message.

  • Pay clears the EU Blue Card threshold

    The advertised pay is over the €41,356 bar, so the route exists if BeOne Medicines uses it.

More jobs over the Blue Card threshold

Skills

Requirements

Nice to have

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

Pay & benefits

What you'll get

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

The role

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.

What you'll do

  • 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

About BeOne Medicines

BeOne Medicines, formerly known as BeiGene, is a global biotechnology company focused on developing and commercializing innovative cancer treatments. With a mission to make oncology medicines more accessible and affordable worldwide, the company operates across the entire value chain, from research and development to manufacturing and commercialization. BeOne Medicines has a significant global footprint, with teams across North America, Europe, Asia, and other regions, and is recognized as a key player in the oncology space.

In Spain, BeOne Medicines has established a presence to support its clinical development and commercial activities, with roles based in Madrid and Barcelona. The company is actively expanding its operations in Europe, and its Spanish offices contribute to global clinical trials and medical affairs. For international professionals, BeOne Medicines offers an opportunity to work in a fast-paced, science-driven environment with a mission to impact cancer care globally. The company values diversity and collaboration, and its Spanish teams work closely with global counterparts, making it an attractive option for those looking to advance their careers in the biotech industry.

Founded
2010
Employees
10,000+
Headquarters
Basel, Switzerland
In Spain
Madrid, Barcelona

Good to know if you are moving

  • BeOne Medicines has a global presence with offices in multiple countries, including Spain, offering opportunities for international mobility.
  • The company is focused on oncology, a high-impact therapeutic area, providing meaningful work for professionals in clinical research and medical affairs.
  • Spain is a key market for clinical trials, and the company's Spanish offices are involved in global studies, offering exposure to international projects.
  • The company offers a collaborative and science-driven culture, with a strong emphasis on innovation and patient impact.
  • As a global biotech, BeOne Medicines provides competitive compensation and benefits, and supports professional development in a growing industry.

In their own words

About the company & team

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.

Additional information

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

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