Contract Specialist, Study Start-up
il y a 4 jours
Job Summary:
Our Site Contracts Team is growing rapidly, and we are currently seeking a full-time, office-based
**Contract Specialist** to join our Site Contracts Team in France. This position plays a key role in the study start-up and clinical trial management processes at Medpace. As a Site Contract Specialist, you will have full responsibility for the life cycle of each contract through the preparation, negotiation, and finalization of contracts. If you want an exciting career where you use your previous expertise and can develop and grow your career even further within a global environment, then this is the opportunity for you
Responsibilities:
- 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 escalate 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 degree; preferably in Law or Sciences.
- At least 1 year of relevant work experience;
- Prior contract negotiation experience preferred but not required;
- Strong attention to detail; and
Strong French and English written and spoken communication skills
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?:
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
**Perks**:
- Flexible work hours
- WFH opportunities
- Career development
- Annual salary review
- Working environment: join a motivated team in our new offices based near Lyon Part-Dieu station
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