With direction from manager, initiate workload, weekly summaries and other reports from CRM.
Meets timelines by establishing priorities and target dates for information gathering, writing, review, and approval; enters and monitors tracking data;
With direction from manager, may assist with follow-up to various internal departments to coordinate contract management activities as needed
Maintains all contracts and related documents in MMS databases/secure repository.
Tracks and follows-up on pending contracts as needed and updating tracking system with each status change.
Minimum Requirements
Master s degree in science, or similar is preferred or relevant work experience.
3-5 years experience in contract management in CRO or similar field required.
Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
Prior experience in CROs/ Pharmaceutical Services and scientific and clinical data/terminology, and the drug development required.
Budget preparation experience preferred
Strong organizational skills and extremely detail oriented.
Efficient time management skills; Ability to handle multiple work assignments concurrently; Ability to coordinate and prioritize conflicting deadlines.
Strong computer skills in Microsoft Office Suite, Adobe, etc.
Strong written and verbal communication skills and the ability to work with many unique personalities.
Familiarity with current ISO 9001 and ISO 27001 standards preferred.
Familiarity with 21 CFR Part 11, FDA, and GCP requirements.