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Associate Director, Group Lead, Data Management Reporting and Analytics
Associate Director, Group Lead, Data Management Reporting and AnalyticsPfizer • La Jolla, California, USA
Associate Director, Group Lead, Data Management Reporting and Analytics

Associate Director, Group Lead, Data Management Reporting and Analytics

Pfizer • La Jolla, California, USA
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ROLE SUMMARY

As part of the Clinical Data and Information Sciences (CDIS) group an integral delivery unit within the Clinical Development & Operations (CD&O) organization the Group Lead is responsible for the collection documentation and programming of study and asset level data cleaning and monitoring report requirements. The Group Lead works closely with the Program Lead (Reporting and Analytics) and CDS Therapeutic Area (TA) Leads to ensure the CDS team functions as a harmonized unit with consistent timely and high quality application of process and delivery of CDS Group Lead will also support CDS and Statistical Data Sciences & Analytics (SDSA) data deliverables from acquired companies. This role has additional line management responsibilities supporting development system / technical processes resources and colleague development. The Group Lead will also be accountable for the timely and high quality deliverables supporting the Pfizer portfolio.

ROLE RESPONSIBILITIES

  • Works closely with CDIS and SDSA department roles and cross-functional study team members to create reporting and analytics solutions that support the quality and timely delivery of data management reports and visualizations required per standard and study specific data review plans.
  • Delivers data analysis reporting operational services to CD&O and other groups within Pfizer
  • Supports business reporting solutions for CD&O inclusive of presenting and communicating results that improve performance
  • Creates any needed documentation for reports throughout the lifespan of the study and or asset for all DMRA deliverables and ensures proper filing in the Trial Master File filings when appropriate.
  • Complies with applicable SOPs and work practices
  • Serves on the data standards board as needed and leads as needed implementation and where needed development of data management reporting standards.
  • Serve as a technical resource to the study teams for data visualization and reporting tools
  • Ensure operational excellence in collaboration with partners and colleagues for application of standards and develop data cleaning reports in support of the data review plan in collaboration with the Clinical Data Scientist ensure operational excellence across all CDIS and SDSA deliverables
  • Directly supports knowledge development of others on reporting and analytics tools that support the accuracy and integrity of study data
  • 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 results
  • Recognizes development needs and identifies / creates development opportunities within own team
  • Develops a talent base and anticipates development needs within the area of responsibility

BASIC QUALIFICATIONS

  • Bachelors degree in Statistics Biostatistics Mathematics Computer Science or related field with 5 to 7 years relevant experience in a pharmaceutical biotech CRO or Regulatory Agency OR Masters or doctoral degree w Five or more years of relevant experience in a pharmaceutical biotech CRO or Regulatory Agency
  • 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
  • Strong communication (written and oral) leadership decision-making influencing negotiation and project management skills
  • Supervisory experience required with emphasis on managing employees remotely located
  • Demonstrated experience managing complex projects and developing successful partnerships within and across functional areas
  • Technical skills and experience using relational databases (e.g. MS SQL Server MS Access or Oracle) SAS and data visualization tools (e.g. Spotfire jReview)
  • Proficiency in the use of Microsoft Office Suite of tools (Outlook Word Excel etc.)
  • PREFERRED QUALIFICATIONS

  • Preference provided to those with programming specifically SQL Python and other visualization tools hands-on experience
  • Candidate demonstrates a breadth of diverse leadership experiences and capabilities including : the ability to influence and collaborate with peers develop and coach others oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
  • PHYSICAL / MENTAL REQUIREMENTS

  • Flexibility to accommodate different time zones within International Units
  • Primarily an office-based position involving sitting in front of a computer for large periods of work time making presentations etc.
  • Work Location Assignment : Hybrid must be on site an average of 2.5 days per week.

    The annual base salary for this position ranges from $120800.00 to $201400.00.

  • In addition this position is eligible for participation in Pfizers Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of lifes moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution paid vacation holiday and personal days paid caregiver / parental and medical leave and health benefits to include medical prescription drug dental and vision coverage. Learn more at Pfizer Candidate Site U.S. Benefits (). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa FL or any location outside of the United States.
  • The annual base salary for this position in Tampa FL ranges from $108700.00 to $181100.00.
  • Relocation assistance may be available based on business needs and / or eligibility.

    Sunshine Act

    Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care providers name address and the type of payments or other value received generally for public disclosure. Subject to further legal review and statutory or regulatory clarification which Pfizer intends to pursue reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse your name address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter please do not hesitate to contact your Talent Acquisition representative.

    EEO & Employment Eligibility

    Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race color religion sex sexual orientation age gender identity or gender expression national origin disability or veteran status. Pfizer also complies with all applicable national state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.

    Pfizer endeavors to make to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and / or interviewing please email . This is to be used solely for accommodation requests with respect to the accessibility of our website online application process and / or interviewing. Requests for any other reason will not be returned.

    Medical

    Required Experience :

    Director

    Key Skills

    Business Development,Information Technology,Oversight,Professional Development,Account Management,Client Relationships,Project Management,Strategic Initiatives,Ensure Compliance,Program Development,KPI,Product Development,Direct Reports,Strategic Development,Special projects

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

    Monthly Salary Salary : 120800 - 201400

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