Entry/Senior Contract Specialist

Medpace; London; On-site; GBP 35,000 - 55,000; Full time

Job summary

An established industry player is looking for a dedicated Contract Specialist to join their dynamic Clinical Operations team in London. This full-time role offers the chance to play a vital part in the study start-up and clinical trial management processes. You will oversee negotiations, finalize contracts, and collaborate with various internal stakeholders to ensure successful project execution. If you are detail-oriented and passionate about making a difference in the clinical research field, this is the perfect opportunity for you to grow your career in a supportive environment that values professional development.

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

Qualifications

• Bachelor's degree in Business Administration, Management, Life Science, or Law required.
• Strong attention to detail and excellent communication skills are essential.

Responsibilities

• Oversees negotiations of clinical study agreements and drives document finalization.
• Acts as subject matter expert for CSA elements and advises stakeholders.

Skills

Contract Negotiation

Communication Skills

Attention to Detail

Education

Bachelor's degree in Business Administration

Bachelor's degree in Management

Bachelor's degree in Life Science

Bachelor's degree in Law

Job description

Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Contract Specialist to join our Clinical Operations team in London. This position plays a key role in the study start-up and clinical trial management processes at Medpace. The Site Contract Specialist will advance the start-up of our projects. 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

• Oversees negotiations of clinical study agreements (CSA´s) on a study level and drives CSA document finalization and execution, including contractual language & terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract & budget negotiators.
• Acts as first-line subject matter expert for all such CSA elements on assigned studies for internal stakeholders. Advises stakeholders on issue resolution within the context of assigned studies.
• Plans contract execution strategy for assigned studies-including forecast of site-specific contractual execution timelines with as much accuracy as possible and coordinates with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations overall.
• Works closely with internal stakeholders to prepare site contractual templates, including payment terms, in order to drive successful negotiation of contracts and budgets.
• Maintains document status reports, and updates department tools/systems and team members on a regular basis;
• Collaborates with internal legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues.
• Manages site level discussions with internal team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites.

Qualifications

• Bachelor's degree in Business Administration, Management, Life science or Law.
• Relevant work experience within the industry or similar preferred but not necessary.
• Prior contract negotiation experience preferred.
• Strong attention to detail and excellent communication skills;

Travel:None

We kindly ask to submit applications in English. We would appreciate if you could indicate the status of your work permit if needed.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• 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

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

EO/AA Employer M/F/Disability/Vets

• Bachelor's degree in Business Administration, Management, Life science or Law.
• Relevant work experience within the industry or similar preferred but not necessary.
• Prior contract negotiation experience preferred.
• Strong attention to detail and excellent communication skills;

Travel:None

We kindly ask to submit applications in English. We would appreciate if you could indicate the status of your work permit if needed.

• Oversees negotiations of clinical study agreements (CSA´s) on a study level and drives CSA document finalization and execution, including contractual language & terms, financial attachments, and investigator grant budgets in collaboration with a global team of site contract & budget negotiators.
• Acts as first-line subject matter expert for all such CSA elements on assigned studies for internal stakeholders. Advises stakeholders on issue resolution within the context of assigned studies.
• Plans contract execution strategy for assigned studies-including forecast of site-specific contractual execution timelines with as much accuracy as possible and coordinates with internal study team stakeholders to ensure that CTA strategy is aligned with overall study start-up plans and expectations overall.
• Works closely with internal stakeholders to prepare site contractual templates, including payment terms, in order to drive successful negotiation of contracts and budgets.
• Maintains document status reports, and updates department tools/systems and team members on a regular basis;
• Collaborates with internal legal, finance and clinical operations departments, including communicating and explaining legal and budgetary issues.
• Manages site level discussions with internal team stakeholders around fair market value of investigator budgets and payment terms within corporate and industry standards during negotiation with sites.