FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Consultant, Preclinical Pharmacokinetics
Ividata Life SciencesConsultant en Pharmacocinétique (PK) Préclinique au sein d'IVIDATA Life Sciences. Évoluer dans un environnement stimulant et collaboratif, avec un fort impact sur les missions.
About the role
Key responsibilities & impact- Draft and review preclinical study synopses
- Coordinate the operational execution and logistics of studies with CROs
- Analyze and interpret bioanalytical data
- Ensure compliance with protocols and timely delivery of study reports
- Assess CRO technical capabilities, negotiate and manage contracts
- Contribute to the collection of PK/PD data and the nonclinical PK strategy
- Review and validate TK/PK documents for regulatory submissions
Requirements
What you’ll need- Minimum 2 years' experience managing preclinical studies
- Expertise in in vivo PK analysis and CRO management
- Master's degree (or equivalent) or Ph.D. in a scientific discipline
- In vivo pharmacokinetic analysis of small molecules
- Proficiency with PK software (e.g., Phoenix)
Benefits
Comp & perks- Stimulating work environment
- Collaborative team environment
- Significant impact on project outcomes
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
preclinical study managementbioanalytical data analysisin vivo pharmacokinetic analysisPK/PD data collectionTK/PK document validationCRO managementcontract negotiationregulatory submission preparation
Soft Skills
coordinationcommunicationorganizational skills
Certifications
Master's degreePh.D.