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Manager, Clinical Data Scientist, Clinical Data Sciences

5+ years
Not Disclosed
10 Dec. 26, 2024
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Manager, Clinical Data Management
Department: Medical
Work Location Assignment: On Premise


Why Patients Need You

Pfizer Worldwide Medical and Safety teams are essential in delivering evidence-based medical support and enabling better health and treatment outcomes. By ensuring our data and evidence are scientifically sound, unbiased, and comprehensive, these teams empower healthcare decisions for the safe and appropriate use of medicines, ultimately improving patient care worldwide.


What You Will Achieve

As a Manager, Clinical Data Management, you will lead efforts to ensure strong ownership, control, and visibility of clinical data. You will play a key role in organizing and validating patient data, ensuring its accuracy and timely delivery to relevant teams. Additionally, you will guide operational teams, forecast resource requirements, and advance new methodologies. Your leadership and planning skills will support Pfizer’s mission to achieve new milestones and transform patients' lives.


How You Will Achieve It

  • Lead and manage projects, providing guidance and planning resource requirements for divisional initiatives.
  • Ensure compliance with Standard Operating Procedures (SOPs) and working practices, including work performed by external providers.
  • Promote the use of efficient, high-quality processes to meet deliverables and timelines.
  • Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials, overseeing all Data Monitoring and Management (DMM) activities.
  • Act as a technical resource for study teams, providing expertise in data visualization, reporting tools, and technology systems.
  • Collaborate with partners to ensure operational excellence in standards application, data acquisition, proactive data review, and data integrity.
  • Partner with research units and external DM service providers to deliver high-quality data management for assigned studies.
  • Conduct central monitoring activities, including system output reviews, proposing signal management actions, and tracking resolutions with study teams.
  • Plan and execute effective communication strategies for engaging customer populations.

Qualifications

Must-Have:

  • Bachelor’s Degree.
  • 5+ years of experience in the pharmaceutical industry or a health information management role.
  • Knowledge of all clinical trial phases and ability to interpret study requirements from protocol reviews.
  • Understanding of FDA and ICH GCP standards and related regulatory requirements.
  • Strong project and risk management skills.
  • Proficient in Windows and associated applications.
  • Exceptional verbal and written communication skills, with the ability to handle multiple tasks and projects.

Nice-to-Have:

  • Master’s Degree.
  • Experience with Contract Research Organizations (CROs) and vendor oversight.
  • Proficiency with commercial clinical data management systems and/or Electronic Data Capture (EDC) products.

About Pfizer

Purpose:
Pfizer is committed to breakthroughs that transform patient lives. Guided by our values—courage, joy, equity, and excellence—we aim to lead in innovation and deliver exceptional outcomes globally.

Equal Employment Opportunity:
Pfizer celebrates diversity and inclusivity, fostering a culture that empowers employees and drives excellence in patient care.


Medical
#LI-PFE

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