Title:
Sr. Clinical Data Manager
Company:
i3 Statprobe (a UnitedHealth Group company)
Location:
any i3 Statprobe office - Ann Arbor, MI, Austin, TX, Basking Ridge, NJ, Cary, NC, Eden Prairie, MN, Lexington, KY, San Diego, CA or Burlington, Ontario, Canada.
Salary:
dependent upon experience
Job Description:
i3 Statprobe focuses exclusively on providing the pharmaceutical and biotechnology industries with comprehensive, integrated data service solutions that include data capture, summary, analysis and reporting for clinical trials across all phases of research.
The Sr. Clinical Data Manager leads data management activities for projects involving multiple and/or complex clinical studies, including global studies.
Responsibilities
- Assumes overall responsibility for the successful execution of the clinical data management projects assigned to them
- Creates, reviews and / or approves all required study documentation
- Performs any data management activities related to projects, as needed
- Provides leadership and supervises data management staff assigned to work on their projects
- Monitors the progress and quality of all data management activities for the project to ensure project timelines are met
- Serves as data management contact with Sponsor, managing expectations and responding to out-of-scope work
- Provide input into proposals and client presentations as needed
Qualifications
- Bachelor's degree and 3 -5 years of Data Coordination experience required, including a working knowledge of clinical trial processes with emphasis on data collection and reporting of clinical trial data
- Knowledge of disease states and medical terminology
- Demonstrated ability to manage multiple tasks with strong attention to detail and accuracy of work
- Demonstrated teamwork skills and ability to influence others
- Demonstrated ability to quickly learn technical databases
- Excellent written and verbal communication skills
- Strong knowledge of MS Office suite is required and knowledge of ClinTrial and/or Inform is preferred
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