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Associate Data Manager - Clinical Data Sciences

2+ years
Not Disclosed
10 Dec. 24, 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: Associate, Clinical Data Management
Company: Pfizer
Location: On Premise

About Pfizer:

Pfizer is a global leader in the pharmaceutical industry, committed to advancing the development and use of medicines that improve patient health and treatment outcomes. Worldwide Medical and Safety colleagues at Pfizer work to connect evidence-based medical support with healthcare decisions, ensuring the safe and appropriate use of medicines.

Job Overview:

As an Associate in Clinical Data Management, you will play an important role in overseeing clinical data, ensuring its accuracy, consistency, and timely processing. This position involves managing clinical data across multiple therapeutic areas and will require you to collaborate with both internal and external stakeholders to support clinical teams. You will assist with data management plans, validation, and preparation, contributing to successful project execution.

Key Responsibilities:

  • Data Management: Participate in Data Monitoring and Management (DMM) activities, including data review and query management.
  • Database Design: Ensure quality database design, including testing, validation, and implementation of clinical data collection tools.
  • Customer Support: Serve as the first point of contact for Clinical Trial Management System (CTMS) inquiries and troubleshooting.
  • Compliance: Ensure all work complies with applicable Standard Operating Procedures (SOPs) and regulatory guidelines.
  • Issue Resolution: Investigate discrepancies, flags, and data issues, liaising with study teams and stakeholders to resolve them.
  • Collaboration: Work closely with study teams, document owners, and other team members to ensure timely and accurate project deliverables.
  • Process Improvement: Contribute to process improvement and assist with other projects that arise within the team.

Qualifications:

Must-Have:

  • Bachelor’s Degree (required).
  • Knowledge or experience with ICH/GCP (International Council for Harmonization/Good Clinical Practice) documentation requirements.
  • Hands-on experience with electronic documentation management systems and/or web-based data management systems.
  • Understanding of the clinical development process and Good Clinical Practice principles.
  • Awareness of regulatory requirements and data standards.
  • Detail-oriented with a commitment to excellence.
  • Strong verbal and written English communication skills.
  • Proficiency with Microsoft Office Suite (Word, Excel, PowerPoint).

Nice-to-Have:

  • Experience in the management of medical and clinical study records and documentation.

Why Pfizer?

Pfizer is dedicated to improving global health by providing high-quality medicines. This position offers an exciting opportunity to work with cutting-edge clinical data management processes in a collaborative environment. By contributing to the success of clinical trials, you will help Pfizer make significant strides in delivering transformative therapies to patients worldwide.

Equal Opportunity Employer:

Pfizer is an equal opportunity employer and complies with all applicable employment laws in the jurisdictions in which it operates.

Work Location: On Premise
Job Posting ID: #LI-PFE


For more details or to apply, visit Pfizer’s career page.