Junior Contract Specialist, Clinical Trials Start-Up

Medpace; Vlaams-Brabant; Vor Ort; EUR 45.000 - 65.000; Vollzeit

Benefits dieser Stelle

Competitive compensation

Comprehensive health, wellness, and 退休

PTO benefits

Office-based with occasional WFH after

Zusammenfassung

Medpace Leuven is seeking a Contract Specialist to manage the full life cycle of Clinical Site Agreements for our trial programs. You will draft, negotiate, and finalize CSA for studies and act as the country expert on strategy and timelines in a global CRO setting.

Entry and experienced candidates are invited to apply. This role emphasizes strong Dutch and English communication, attention to detail, and the ability to collaborate with internal teams and external partners.

Qualifikationen

• Bachelor's degree in Law or Sciences.
• 1 year of relevant work experience preferred.
• Prior contract negotiation experience preferred but not required.
• Strong Dutch and English written and spoken communication skills; French is a plus.
• Ability to work in a team environment and independently.
• Strong attention to detail.

Aufgaben

• Drafting, reviewing, negotiating, and finalizing Clinical Site Agreements or other Site-specific legal agreements required for a clinical study.
• Act as first-line subject matter expert for your country regarding CSA strategy, timelines and expectations for all such CSA execution elements and challenges.
• Negotiate within client approved contract and budget templates and negotiation parameters.
• Build strong site/external stakeholder relationships to accelerate Site contract negotiations.
• Identify and assesses legal, financial, and operational risks and elevate to appropriate Contract Lead/Contract Manager or other internal stakeholders.
• 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 timelines.
• Keep up to date with applicable local regulations impacting clinical trial contracts.

Kenntnisse

Dutch & English

Attention to detail

Communication skills

Organizational skills

Teamwork

Independent work

Negotiation

French a plus

Ausbildung

Bachelor's degree in Law or Sciences

Jobbeschreibung

Medpace Leuven is seeking a Contract Specialist to manage the full life cycle of Clinical Site Agreements for our trial programs. You will draft, negotiate, and finalize CSA for studies and act as the country expert on strategy and timelines in a global CRO setting.

Entry and experienced candidates are invited to apply. This role emphasizes strong Dutch and English communication, attention to detail, and the ability to collaborate with internal teams and external partners.