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Manager, Clinical Data Scientist, Clinical Data Sciences

5+ years
Not Disclosed
10 Dec. 23, 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

Manager, Clinical Data Management - Pfizer

About the Opportunity:

At Pfizer, Worldwide Medical and Safety teams connect evidence-based, medical decision support with colleagues and stakeholders to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. As a Manager in Clinical Data Management, you will be essential in processing, reviewing, and organizing patient data, ensuring the delivery of accurate, timely, and consistent clinical data to medical teams and other stakeholders. Your role will strengthen clinical data oversight, playing a critical part in advancing healthcare outcomes and the development of life-saving treatments.


What You Will Achieve:

In your role as a Manager, Clinical Data Management, you will:

  • Lead Projects & Guide Teams: Provide guidance and manage project timelines, resource planning, and operational activities to meet objectives and ensure the efficient execution of projects.
  • Data Management: Serve as Clinical Data Scientist and Trial Lead for one or more clinical trials, overseeing all Data Monitoring and Management (DMM) activities, including data acquisition, review, and validation.
  • Technical Expertise: Act as a technical resource for study teams, providing support for data visualization, reporting tools, and system processes.
  • Ensure Operational Excellence: Collaborate with internal and external teams to uphold standards, ensure data integrity, and proactively address data-related issues across clinical studies.
  • Central Monitoring & Analysis: Conduct central monitoring, reviewing system outputs and proposing action management strategies to ensure the resolution of any data discrepancies.
  • Effective Communication: Lead communication strategies to engage stakeholders, ensuring transparency and coordination across study teams and other groups.

Qualifications:

Must-Have:

  • Education: Bachelor’s Degree in a relevant field.
  • Experience: 5+ years of experience in the pharmaceutical industry or health information management.
  • Knowledge: Familiarity with all phases of clinical trials, as well as FDA, ICH-GCP, and related regulatory requirements.
  • Project & Risk Management: Demonstrated ability to manage projects and risks effectively while meeting deadlines.
  • Communication Skills: Strong verbal and written communication abilities, with a proven track record of handling multiple tasks and projects.
  • Technical Skills: Proficiency with Windows applications.

Nice-to-Have:

  • Education: Master's Degree.
  • Experience: Experience in Contract Research Organization (CRO) and vendor oversight.
  • Technical Expertise: Familiarity with commercial clinical data management systems and/or EDC products.

Work Location:

  • On Premise

Why Pfizer:

Pfizer is committed to being an equal opportunity employer and complies with all relevant employment legislation in every jurisdiction we operate. By joining Pfizer, you’ll have the opportunity to play a part in making new milestones in medicine and improving patient outcomes globally.


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