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Associate Data Manager - Clinical Data Sciences

2+ years
$64,600.00 to $107,600.00
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 an Associate Clinical Data Management role at Pfizer, focused on supporting the clinical data management process by ensuring accurate, timely, and consistent clinical data is collected, reviewed, and shared with the relevant teams.

Key Responsibilities:

  1. Data Management and Oversight:

    • Assist with the completion of project milestones and deadlines.
    • Participate in Data Monitoring and Management (DMM) activities, including data review and query management.
    • Ensure quality database design and validation, testing clinical data collection tools.
    • Serve as the first point of contact for Clinical Trial Management System (CTMS) related inquiries.
  2. Collaboration and Problem Solving:

    • Liaise with the Study Team Point of Contact and other relevant team members to resolve document discrepancies and issues.
    • Investigate any potential discrepancies and work with the study team to verify findings.
    • Contribute to process improvements and support other projects.
  3. Quality Assurance:

    • Ensure compliance with Pfizer’s Standard Operating Procedures (SOPs) and working practices.
    • Investigate logic check flags and ensure the integrity of the data.

Qualifications:

  • Must-Have:

    • Bachelor’s degree.
    • Knowledge or experience with ICH/GCP documentation requirements and electronic documentation systems.
    • Understanding of regulatory requirements and clinical development processes.
    • Strong attention to detail, with proficiency in Microsoft Office Suite.
    • Strong communication skills in both oral and written English.
  • Nice-to-Have:

    • Experience in managing clinical study records and documentation.

Other Job Details:

  • Deadline to Apply: January 3, 2025.
  • Work Location: Flexible. Colleagues work 2-3 days weekly on-site and may work offsite as needed.
  • Salary Range: $64,600 - $107,600 annually, with eligibility for a 7.5% bonus based on Pfizer’s Global Performance Plan.
  • Benefits: Comprehensive benefits, including 401(k) matching, medical, prescription, dental, and vision coverage.

EEO & Employment Eligibility:

Pfizer is an equal opportunity employer and complies with all relevant laws regarding non-discrimination, work authorization, and employment eligibility verification.

Sunshine Act:

Pfizer complies with federal and state transparency laws that require the reporting of certain payments and transfers of value to healthcare providers.

This role is a great opportunity for someone with a strong attention to detail and interest in clinical data management, contributing to the overall success of Pfizer’s clinical trials and helping improve patient outcomes.

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