Reports to: Project Manager
Location: West Central Indiana
Position Summary (non-exhaustive list):
Missions:
- To ensure R&D studies direction according to the Amatsigroup Inc SOPs and the GLP, 21 CFR Part 58, including multisite studies (OECD Principles of Multisite studies, Chapter no. 13)
- To ensure the completion and the follow-up of R&D studies according to the GLP, 21 CFR Part 58
- To ensure a scientific and technical assistance
- To contribute to the compliance with legislation related to the animal experimentation
- To participate to the management of the In-life unit
Main Responsibilities:
- To perform the CRO studies as Study Director
- To ensure the set-up and the completion of the study according to the Master schedule and according to the GLP, 21 CFR Part 58
- To ensure the drafting and finalization of the study documents (study protocols, reports, …)
- To ensure the customers care during the studies
- To ensure the animal welfare (according to the IACUC and the USDA requirements)
- To ensure or oversee the animal clinical examinations, the treatments and the samplings
- To work with companion and farm animals
- To participate to the choice of new equipment and materials
Skills:
- Higher education (College or University) / DVM or relevant professional experience
- R&D (Research & Development) experience on medical products
- Experience in performing studies according to GLP, 21 CFR Part 58 and OECD Principles of Multisite studies, Chapter no. 13
- Organization, good interpersonal skills, meticulousness, preciseness and good writing skills (Good knowledge of Microsoft Office)
- US legislation on the animal experimentation
Salary:
Negotiable based on the experience
Position Deadline:
ASAP
