Salary
💰 $136,200 - $197,400 per year
About the role
- Lead End to End Data Management activities with hands on ability to manage outsourced studies
- Represent Data Management function in Clinical Study Meetings
- Work with CRO and Recursion functional groups to complete EDC set up, database migrations /UAT and other systems
- Establish Vendor Oversight Plans for all studies
- Serve as a SME for various operational activities and DM processes
- Leads/Oversee the creation and maintenance of Data Management documents
- Accountable for coordination with other functional groups for submission related activities
- Manage strategic input into the design of data flow across EDC and non-EDC data sources
- Ensure Filing, archival and inspection readiness of all Data Management Trial Master File activities
Requirements
- Bachelor’s degree in science, math or computer science
- 8 - 12+ years’ experience in the biopharmaceutical industry
- Experience managing external data and 3rd party vendors
- Strong knowledge of regulations and guidelines that apply to the conduct of clinical trials
- Excellent written and verbal communication skills and ability to work collaboratively as a part of a team
- Comprehensive benefits package
- Annual bonus
- Equity compensation
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
data managementEDC setupdatabase migrationsUATvendor oversightdata flow designfilingarchivalinspection readinessclinical trial documentation
Soft skills
communicationcollaborationleadershipteamworkaccountabilityproblem-solvingorganizational skillsstrategic thinkingattention to detailstakeholder management