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Senior Associate, Senior Data Manager

3+ 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

Senior Associate, Data Management - Pfizer

About the Opportunity:

At Pfizer, our Worldwide Medical and Safety teams play a vital role in supporting healthcare decisions and ensuring the safe use of medicines. As part of our mission, we are looking for a Senior Associate in Data Management to oversee the accuracy, timeliness, and quality of clinical data. You will contribute to the success of clinical trials by managing data monitoring and management activities, collaborating with various stakeholders, and ensuring operational excellence across all data-related deliverables.


What You Will Achieve:

As a Senior Associate, you will:

  • Data Management: Serve as Data Manager for one or more clinical trials, ensuring data monitoring and management (DMM) activities are carried out effectively.
  • Operational Excellence: Collaborate with internal teams and external partners to ensure standards are met, producing data cleaning reports and performing data reviews.
  • Quality Assurance: Ensure the quality and completeness of data through listing setups and testing, according to the Data Management Plan.
  • Collaboration & Communication: Build strong relationships with local and global subject matter experts (SMEs), leveraging their expertise to proactively identify and solve issues.
  • Knowledge Sharing: Document lessons learned during studies and share insights with other teams to facilitate cross-study learning.

Qualifications:

Must-Have:

  • Education: Bachelor's Degree required.
  • Experience: 3+ years in data management or related field.
  • Technical Skills: Experience with web-based data management systems and electronic document management systems.
  • Regulatory Knowledge: Familiarity with International Conference on Harmonization (ICH) and Good Clinical Practices (GCP).
  • Clinical Study Management: Strong understanding of clinical study management processes and regulatory operations.
  • Communication: Excellent verbal and written communication skills, with the ability to adapt messaging to different audiences.

Nice-to-Have:

  • Education: Master’s Degree.
  • Industry Experience: Experience in the pharmaceutical industry.
  • Technical Skills: Familiarity with data visualization tools and clinical data management systems.
  • Regulatory Knowledge: Awareness of regulatory requirements and data standards.

Work Location:

  • On Premise

Why Pfizer:

Pfizer is an equal opportunity employer, committed to diversity and inclusion across all levels. We are dedicated to helping improve the lives of patients around the world. Join our team to be part of an innovative organization focused on scientific excellence and improving health outcomes.


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