Contract Specialist Info Session - Europe - November 30th

Medpace; Belgique; Remote; EUR 53,000 - 80,000; Full time

Benefits offered by this job

Competitive compensation programs

Comprehensive health, wellness, and 1/

Office based culture with occasional W

Company-sponsored social events

Job summary

Medpace is hosting a virtual information session about Contract Specialist roles across Europe, including London, Munich, Warsaw, Prague, and Leuven. The office-based opportunities target individuals with diverse backgrounds in contracts, law, or procurement and aim to advance clinical research contracts.

Selected candidates may receive a Teams invite for the online event. Responsibilities include drafting and negotiating agreements, managing risk, and coordinating with internal departments to

Qualifications

• Strong language proficiency in English and the local language.
• Office-based work readiness.

Responsibilities

• Drafting, reviewing, negotiating, and finalizing contracts and related documents for clinical studies.
• Negotiate within client-approved templates and parameters.
• Identify legal, financial, and operational risks and escalate as needed.
• Provide recommendations and alternative resolutions during negotiations.
• Coordinate with internal teams to align site start-up activities with contractual timelines.
• Stay updated on local regulations affecting clinical trial contracts.

Skills

Language proficiency

Education

Bachelor's/Master's/PhD in Business or Law

Job description

Interested in a career where contracts, negotiation, and clinical research come together?

Medpace is hosting a virtual information session for individuals interested in learning more about our Contract Specialist opportunities across Europe. During this session, you'll learn more about our office-based Clinical Contract Specialist opportunities at Medpace, with openings in London, Munich, Warsaw, Prague, and Leuven. Whether you are an early-career professional or bringing transferable experience from another industry, join us to learn more about a career in clinical research contracts.

WHEN: November 30th at 11:00 AM

A first pre-screening will be done and if you're selected you will receive a MS Teams invite to follow the online event.

Responsibilities

The Contract Specialists are in charge of

• Drafting, reviewing, negotiating, and finalizing agreements, termination letters or other legal documents required for a clinical study;
• Negotiate within client approved contract and budget templates and negotiation parameters;
• Identify and assesses legal, financial, and operational risks and escape to appropriate Contract Lead or Contract Manager;
• Provide recommendations and alternative resolutions throughout negotiations using established escalation channels;
• Coordinate with internal functional departments to ensure various site startup activities are aligned with contractual process and mutually agreed up timelines; and
• Keep up to date with applicable local regulations impacting clinical trial contracts.

Qualifications

• Bachelor's, Master's or PhD graduate in Business, Law or related fields;
• or an experienced professional with transferable contract, legal, procurement or commercial experience;
• Strong language proficiency in English and the local language;
• Willing to work office-based.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.

Why Medpace?

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

Purpose-Driven Work

• Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture

• Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
• Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development

• Office based environment with on-site mentors
• Defined career paths with clear advancement opportunities
• Industry renowned onboarding and training programs designed to accelerate professional development
• Ongoing training and continuous learning opportunities throughout your career
• An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits

• Competitive compensation programs that recognize and reward performance
• Comprehensive health, wellness, retirement, and PTO benefits
• Office based culture with occasional WFH that provides flexibility for eligible positions after training
• Company-sponsored social events

Please note benefits may vary based on country.

What to Expect Next

A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.