FREE ACCESS
5,000–10,000 jobs/day
See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Tech Stack
Tools & technologiesGoogle Cloud PlatformMS SQL ServerOracleSQL
About the role
Key responsibilities & impact- Serves as Clinical Data Scientist and Trial Lead for one or more clinical trials
- Responsible for all CDIS activities including selection and application of data acquisition standards
- May functionally manage a team of Associate Data Managers, Senior Data Managers
- Works with Asset Leads to establish strategy, timelines, and adequate resourcing of DMs
- Ensures appropriate documentation across the lifespan of the study/asset for all DM deliverables
- Provides project management leadership to DM teams
- Acts as the key scientific and technical data management expert
- Serves as Subject Matter Expert (SME) for and oversees the design, documentation, testing and implementation of clinical data collection tools.
- May act as data management contact for regulatory inspections/audits in liaison with the appropriate Quality and Safety groups.
Requirements
What you’ll need- Bachelor’s degree required
- Degree in scientific field preferred
- Minimum 7 years Data Management experience required
- Demonstrated successful experience in all relevant clinical data management activities in a Biopharmaceutical or CRO setting
- Working knowledge of all phases of clinical trials
- Strong Project and Risk Management
- CRO and vendor oversight experience preferred
- Strong verbal and written communication skills
- Knowledge of clinical research, FDA & ICH, GCP, GCDMP, and related regulatory requirements
- Proficient experience using commercial clinical data management systems and/or EDC products (Medidata RAVE, Oracle RDC, Inform preferred)
- Experience using relational databases (e.g. MS SQL Server, MS Access, or Oracle) and data visualization tools (e.g. Spotfire, jReview)
- Strong knowledge of MedDRA/WHO-Drug
- Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.).
Benefits
Comp & perks- Flexible working hours
- Professional development opportunities
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical data managementdata acquisition standardsproject managementrisk managementclinical trial phasesrelational databasesdata visualization toolsMedDRAWHO-Drugclinical data collection tools
Soft Skills
leadershipcommunicationteam managementstrategic planningdocumentationproblem-solvinginterpersonal skillsorganizational skillscollaborationattention to detail