Sr Data Ops Technical Specialist
Full Job Posting
Job Responsibilities
- Required: 7+ years of Data Management experience, with at least 2 years of hands-on experience leading PDM activities/projects.
- Supports DM to ensure processes in relation to systems/databases are consistent and that best
- practices are maintained globally. Can consult with internal functional teams and sponsors as a SME
- Assists with developing, monitoring and enforcing productivity, quality standards and efficiencies, input into the development of project and timeline metrics
- Maintains awareness of potential out of scope work for assigned projects and supports Lead Clinical Data Manager (LCDM) as appropriate
- Participates in and presents at internal, sponsor, third-party, and investigator meetings
- Participates in and supports internal and external audits and inspections
- Supports the development of User Test Plans for data entry screens, electronic edit checks, data listings, import/export programs and medical coding
- Supports the release of tested clinical data databases and updates to the production environment
- Supports the development of CRF and eCRF completion guidelines
- Supports the development and review of specifications for listings and summaries (other than for statistical reporting requirements) from CRF databases and external sources
- Participates in the development of departmental technologies, SOPs, processes and procedures
- Supports and participates in the testing and integration of new technologies within Data Operations
- Maintains documentation on an ongoing basis and ensures that all TMF filing is correct and up to date
- Train and mentor Data Management staff
- Maintains proficiency in Data Management systems and processes through regular training.
- May represent Data Operations in company-wide initiatives
- Performs other work-related duties as assigned. Minimal travel may be required (up to 25%)
Get to know Syneos Health
Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.
http://www.syneoshealth.com
Additional Information
Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
About Syneos Health
Integrated biopharmaceutical solutions from lab to life.
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