Clinical Contracts Manager

il y a 1 semaine


Bruxelles, Région de Bruxelles, Belgique CK Group Temps plein

Job Title: Clinical Contracts Manager

Location: Brussels, Belgium.

Job Type: Full-time, Permanent.

Introduction:

Are you an experienced professional in clinical contracts management? Do you have a passion for ensuring the smooth operation of clinical trials through effective contract negotiation and management? We are seeking a highly motivated Clinical Contracts Manager to join our dynamic team in Brussels, Belgium.

As a Clinical Contracts Manager, you will play a pivotal role in managing and negotiating clinical trial agreements (CTAs) with a variety of stakeholders including clinical research organizations, vendors, and academic institutions. You will contribute to the success of our clinical trials and ensure compliance with local and international regulations.

Key Responsibilities:

  1. Manage the entire lifecycle of clinical trial agreements, including drafting, reviewing, and negotiating contracts.
  2. Collaborate with internal stakeholders (clinical operations, legal, finance) to ensure contract terms are aligned with the company's policies.
  3. Coordinate and negotiate with external parties (investigators, institutions, vendors) to finalize agreements.
  4. Ensure that all contracts comply with legal, regulatory, and ethical standards.
  5. Provide guidance and support to clinical operations teams regarding contractual obligations and amendments.
  6. Monitor contract performance and resolve any issues or disputes in a timely manner.
  7. Assist in preparing and reviewing budgets associated with clinical trials.
  8. Track and report on the status of contract negotiations and renewals.

Required Qualifications:

  1. Bachelor's degree in Law, Life Sciences, or a related field.
  2. Minimum of 5 years of experience in clinical contract management, preferably within a pharmaceutical, CRO, or healthcare environment.
  3. Strong knowledge of clinical trial agreements, clinical operations, and regulatory requirements.
  4. Excellent negotiation, communication, and interpersonal skills.
  5. Fluency in English, with additional language skills in French or Dutch considered a plus.
  6. Detail-oriented with strong organizational skills and the ability to manage multiple priorities.
  7. Ability to work both independently and as part of a team in a fast-paced environment.

What We Offer:

  1. A competitive salary and benefits package.
  2. The opportunity to work with a dynamic and growing team in an innovative company.
  3. A supportive work environment that values professional development and work-life balance.
  4. The chance to be part of exciting and cutting-edge clinical research projects.

How to Apply:

If you are ready to take the next step in your career and join an industry leader, we would love to hear from you Please submit your CV and a cover letter outlining your qualifications and motivation for the role to rangrave@ckqls.ch

Equal Opportunity Employer:
We are an equal opportunity employer and welcome applications from all qualified candidates regardless of race, ethnicity, gender, sexual orientation, disability, or any other characteristic.

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