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Project Manager

3 months ago

Chennai, India Pfizer Full time

About the Company:

Works closely with department roles, assigned mentor, and cross-functional study team members to manage the development cycle of data capture solutions that support the quality and timely delivery of data required per standard and study specific data review plans. Sets objectives for and manages multiple projects/ ongoing work activities of moderate complexity within CDS. Leads cross-functional initiatives as needed; represents CDS/Database Management on cross-divisional initiatives. Solves complex problems, applies previous experience outside of own area. Demonstrates comprehensive industry knowledge; acts as SME. May help to define and/or influence applicable SOPs and work practices. Solves complex problems, applies previous experience outside of own area. Oversees operational activities/projects of professional Work Teams to support short / long-term Department goals. Leads internal initiatives, working with other roles within CDS to improve processes. Represents Database Management on CDS initiatives. Complies with applicable SOPs and work practices. Serve as a project management resource to the study teams for developing and implementing database development project plans. Ensure proper planning of study activities in DBM and proactively alert risk and plan mitigation. Independently, perform Impact analysis for proposed solutions to existing tools and processes and convey the same to technical and non-technical stakeholders. Act as an expert in the area, applying best practices according to documented processes. Participate in Standards meetings as appropriate. Ensure compliance always. Ensure seamless functioning and collaboration of CDS activities between the DBM and Clinical Data Scientist functions. Ensure operational excellence in collaboration with partners and colleagues for application of standards within data capture methods in support of the data review plan, in collaboration with the Clinical Data Scientist, ensure operational excellence across all DMM deliverables. Ensure Quality of DBM Deliverables are on par with Organizational and Department level objectives. Assess impacts of Change Control and develop mitigation plans for emerging risks and issues. Identifies existing process/product improvements. Develops innovative, advanced new concepts that improve processes / products across own and related disciplines. Takes appropriate risks to achieve desired result.


Qualifications:

  • Bachelor's degree in Life Sciences, Computer Science, or equivalent
  • Minimum of 11 years of relevant project management experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions
  • Strong project management, communication (written and oral), decision-making, influencing, and negotiation skills
  • Familiarity with Electronic Data Capture systems, Clinical Data Management Systems/relational databases (e.g. Oracle InForm and Data Management Workbench, MS SQL Server or MS Access) and data visualization tools (e.g. Spotfire, J-Review)
  • Experience with Advanced features of MS Project or other enterprise project management tools


Preferred Skills:

  • Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.)
  • Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable
  • Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
  • PMP Certification