Director, Study Quality and Compliance - Nonclinical Safety/Toxicology
Cambridge (USA)onsitedirector$186K – $345K
Posted today · via Workday
About this role
Job Description Summary Location: Cambridge MA Internal: Director LI#-Hybrid This role oversees the Study Quality and Compliance team within the Toxicology line function of PCS. This team is responsible for: handling samples and data associated with both internally and externally conducted toxicology studies; maintaining departmental SOPs, and oversight of training records for departmental personnel; and interfacing with the archives function to ensure proper storage of toxicology-related materials and records. A major part of this role will be to identify and implement a software system that enables effective tracking and analytics of study-related information that this group is responsible for overseeing.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
We compare your skills against the role requirements.
2
Level fit
This role is director-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Cambridge (USA). We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
More at Novartis
- View →AS&T ExpertKundl
- View →QC Analyst IIKundl
- View →Executive Director, Theranostics Platform EnablementEast Hanover
- View →Radioligand Therapies (RLT) Sales Specialist, Prostate – ConnecticutField Sales (USA)
- View →Director, Translational Medicine Expert (Neurodegeneration)London (The Westworks)
- View →Senior Administrative AssistantEast Hanover