Contract Manager

Medpace; Greater London; On-site; GBP 45,000 - 65,000; Full time

Benefits offered by this job

Flexible work environment

Competitive compensation and benefits package

Competitive PTO packages

Structured career paths with opportunities for professional growth

Company-sponsored employee appreciation events

Employee health and wellness initiatives

Job summary

Medpace is seeking a Contract Manager to join their Clinical Operations team in London. In this role, you will manage clinical study agreements (CSA) for global trials, develop strategies and templates, and ensure timely deliverables are met. The ideal candidate will have a Bachelor's degree in life sciences or a related field, extensive clinical trial experience, and strong negotiation skills. This position offers a flexible work environment, competitive compensation, and structured career development opportunities.

Qualifications

• 3+ years of management or oversight experience.
• CRO experience preferred.
• International Contract and budget negotiation experience.

Responsibilities

• End-to-end management of the clinical study agreement (CSA) process for global, multi-site clinical trials.
• Develop the study-specific CSA strategy with the Sponsor and internal stakeholders.
• Develop country-specific CSA templates.
• Present progress to internal and external stakeholders ensuring deliverables are met within agreed upon timelines.

Skills

Clinical Trial experience

Ability to effectively influence others

Exceptionally strong communication skills

Advanced knowledge of Microsoft Word

Advanced knowledge of Excel

Advanced knowledge of PowerPoint

Education

Bachelor’s degree in life-sciences or relevant legal or business field

Job description

Our clinical operations activities are growing rapidly, and we are currently seeking a Contract Manager to join our Clinical Operations team in London. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you!

Responsibilities

• End-to-end management of the clinical study agreement (CSA) process for global, multi-site clinical trials
• Develop the study-specific CSA strategy with the Sponsor and internal stakeholders
• Develop country-specific CSA templates
• Present progress to internal and external stakeholders ensuring deliverables are met within agreed upon timelines

Qualifications

• Bachelor’s degree in life‑sciences or relevant legal or business field
• Clinical Trial experience
• CRO experience preferred
• International Contract and budget negotiation experience
• 3+ years of management or oversight experience
• Ability to effectively influence others
• Exceptionally strong communication skills
• Advanced knowledge of Microsoft Word, Excel, and PowerPoint

Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives