Vacancy expired!
Job Description
· Assist in the preparation of study protocols, amendments, deviations, data capture forms, test article documentation and study reports
· Collaborate with multiple internal partner groups to plan, coordinate, conduct, analyze, and report studies
· Conduct training of Investigators and other study site personnel
· Serve as the principal communication link between the Sponsor and study sites
· Maintain study files in accordance with SOPs and regulatory requirements
· Assist in data management processes including paper and electronic data capture, entry, review, tracking and verification utilizing electronic tools and centralized data management systems.
· Assist in preparation of study files for submission to regulatory agencies
· Provide clinical updates to project teams and sub-teams
· Assist with animal related study activities (i.e. clinical sampling, test material administration and clinical observations)
Additional Information
Position is full-time, Monday-Friday 8:00 a.m.-5:00p.m., with overtime as needed.Candidates currently living in a commutable distance to Kalamazoo, MI are encouraged to apply.
What we Offer:
Excellent full time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
Vacancy expired!