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Manager, Clinical Data Scientist, Clinical Data Sciences

5+ years
$99,900.00 to $166,500.00
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

This job posting is for a Manager role in Clinical Data Management at Pfizer, focused on the oversight and processing of clinical data to ensure high-quality data management across clinical trials. The position is critical in ensuring accurate, timely, and consistent delivery of clinical data to Pfizer’s medical department and other stakeholders.

Key Responsibilities:

  1. Data Management and Oversight:

    • Lead projects related to clinical data monitoring and management, ensuring alignment with Pfizer’s Standard Operating Procedures (SOPs).
    • Ensure timely data preparation, validation, and reporting, providing guidance to operational teams.
    • Serve as a Clinical Data Scientist and Trial Lead, overseeing all Data Monitoring and Management (DMM) activities.
  2. Collaboration and Communication:

    • Collaborate with study teams, Research/Business Units, and external service providers to ensure data quality and integrity.
    • Engage with customer populations through communication plans and methods for effective data engagement.
  3. Risk and Project Management:

    • Lead risk management activities, including proactive data review and resolving data integrity issues.
    • Plan and manage resource requirements to meet project timelines and objectives.
  4. Technical Expertise and Process Improvement:

    • Serve as a technical resource for data visualization and reporting tools, providing support for technology systems.
    • Promote the use of efficient and consistent processes across all stages of clinical trials.
  5. Operational Excellence:

    • Ensure operational excellence in collaboration with partners, applying standards to data acquisition and management activities.

Qualifications:

  • Must-Have:

    • Bachelor’s Degree and 5+ years of relevant experience, particularly within the pharmaceutical industry or health information management.
    • Knowledge of clinical trials, FDA regulations, Good Clinical Practices (GCDMP), and ICH guidelines.
    • Strong project management and risk management skills.
    • Proficiency in Windows and its applications, along with strong verbal and written communication skills.
  • Nice-to-Have:

    • Master's degree.
    • Experience with Contract Research Organizations (CROs) and vendor oversight.
    • Proficiency in using commercial clinical data management systems or Electronic Data Capture (EDC) products.

Other Job Details:

  • Deadline to Apply: January 17, 2025.
  • Work Location: Hybrid (combination of remote and on-site work).
  • Salary Range: $99,900 - $166,500 annually, with eligibility for a 15% bonus target and participation in Pfizer's share-based long-term incentive program.
  • Benefits: Comprehensive benefits including 401(k) matching, paid vacation, medical, prescription, dental, and vision coverage, among others.

EEO & Employment Eligibility:

Pfizer is an equal opportunity employer, complying with all relevant laws and regulations related to non-discrimination and employment eligibility verification.

Sunshine Act:

Pfizer reports payments and transfers of value to healthcare providers as required by federal and state transparency laws.

This role is pivotal in managing Pfizer’s clinical data, ensuring data quality, integrity, and compliance with regulatory standards to support the development of safe and effective medicines for patients worldwide.