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Clinical Data Team Manager
2 weeks ago
**Life Sciences Team Manager**
**Experience 8to12yrs**
**Mississauga - ON**
**Shift Day GENERAL SHIFT**
**RATE : CAD$60/hr. on Inc/Corp to Corp**
**Required Skills**: Research and Development, Biometrics, Analysis & Reporting of **Clinical trial** data, **Extensive programming in SAS/Equivalent software**
**Technology Life**:
- Sciences
**Job title TEAM MANAGER ( CWR ) - DATA**
**Job summary Team Manager-SP.**
- Graduate/Post Graduate in Mathematics/Statistics/Applied Statistics/Computer Science/Life Sciences.
- This role involves supporting study teams for Analysis & Reporting of Clinical trial data through extensive programming in SAS/Equivalent software, development and validating generalized macros, and to lead single/multiple teams of Statistical Programmers (In team management role) to deliver quality outputs in stipulated timeframe. Mentor, coach & act as SME to the team in develop
**Roles & Responsibilities Team Manager-SP**
- Graduate/Post Graduate in Mathematics/Statistics/Applied Statistics/Computer Science/Life Sciences.
- This role involves supporting study teams for Analysis & Reporting of Clinical trial data through extensive programming in SAS/Equivalent software, development and validating generalized macros, and to lead single/multiple teams of Statistical Programmers (In team management role) to deliver quality outputs in stipulated timeframe. Mentor, coach & act as SME to the team in developing strong analytical and programming skills, troubleshoot technical issue using statistical software SAS/equivalent software. Business / Customer:
- Act as SME for team members in resolving any technical and operational issues.
- Good understanding of the domain and related processes
- Independently interact with client and handle/address any queries from client
- Proactively address issues Technical:
- Programming in SAS for analyzing data and producing Safety and/or Efficacy Tables, Listings and Figures in specified formats as per specifications and in accordance with Statistical Analysis Plan (SAP).
- Creation and review of programming specifications
- Programming in SAS for creation of derived data sets/ADaM as per the specification document
- Performing quality checks for all the reports generated by team members, validation of new/ modified SAS programs and macros
- Ensure the study team is trained on Study documents before initiation of study (as assigned)
- Ability to understand and write complex statistical programming specifications and guide/support other team members in task execution
- Work across cross functional teams to resolve any technical and delivery issues thus ensuring quality of deliverables within stipulated timelines.
- To assist management team in providing status and metrics on deliverables, resource utilization, productivity and quality of deliverable Compliance:
- Adherence to SOPs and GPP
- Ensure teams compliance to organizational policies
**Job Summary/Responsibilities**:
- Participate in developing, reviewing, and providing input for analysis specifications for Real World Data (RWD) analyses;
- Develop and validate statistical analyses and generate outcomes.
- Participate and/or contributes in statistical analysis activities for regulatory authority submissions/inquiries.
- Lead activities of assigned statistical programming, provide guidance to programmers and analysts.
- Participate on global teams that evaluate processes and make suggestions for process and system needs and improvements;
- Work closely with global cross-functional teams;
**Contribute to**:
- Drug research;
- Development of new drugs;
- Approval of new drugs by health authorities;
- The life cycle management and surveillance of marketed drugs;
- Improvement efficiencies in existing data analysis process.
**Regards,**
**Team Compest Solutions Inc**
**D:
+1 647-660-7562
**Job Types**: Full-time, Fixed term contract
Contract length: 12 months
**Salary**: $60.00-$63.00 per hour
Schedule:
- 8 hour shift