Track This Job
Add this job to your tracking list to:
- Monitor application status and updates
- Change status (Applied, Interview, Offer, etc.)
- Add personal notes and comments
- Set reminders for follow-ups
- Track your entire application journey
Save This Job
Add this job to your saved collection to:
- Access easily from your saved jobs dashboard
- Review job details later without searching again
- Compare with other saved opportunities
- Keep a collection of interesting positions
- Receive notifications about saved jobs before they expire
AI-Powered Job Summary
Get a concise overview of key job requirements, responsibilities, and qualifications in seconds.
Pro Tip: Use this feature to quickly decide if a job matches your skills before reading the full description.
Title: Functional Project Manager (Pharmacology &Toxicology and Bioanalytics)
Company: Global Leading CRO/Biotech
Location: Hybrid - Flemish Region, Belgium
Type: 8 months contract - full-time (40 hours per week)
Main Responsibilities
- Track and manage internal and external vendor activities, ensuring delivery against timelines, budgets, and quality expectations.
- Develop and maintain progress, budget, and risk tracking tools; proactively identify and mitigate risks.
- Act as the primary point of contact for external vendors, including meeting coordination and oversight, with occasional site visits.
- Coordinate sample shipments and specialty lab data delivery aligned with clinical trial milestones.
- Drive preparation of source data reports and present progress updates to cross-functional teams and management.
- Ensure accurate financial and procurement system entries and support contracting activities with sourcing and vendor management teams.
Main Requirements
- Degree in life sciences (PhD or MSc, or equivalent experience); level dependent on experience.
- Strong vendor management experience and have a background/education in Labs/bioanalytical technique.
- Background or exposure to animal science, laboratory science, or clinical trials preferred; industry experience a plus.
- Strong organizational and documentation skills with excellent computer proficiency; experience or willingness to learn project planning tools (e.g., MS Project, Planisware).
- Understanding of or willingness to learn GLP/GCP requirements.
Interested? Apply now for immediate consideration or contact Maria Tsalpatourou at [email protected]
ABOUT PLANET PHARMA
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency.
We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
www.planet-pharma.com
Ready to apply?
Join Planet Pharma and take your career to the next level!
Application takes less than 5 minutes

