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Senior Associate, Senior Data Manager

3+ years
Not Disclosed
10 Dec. 27, 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

Senior Associate – Data Monitoring and Management (DMM)


Why Patients Need You

At Pfizer, our Worldwide Medical and Safety colleagues connect evidence-based medical decision-making with stakeholders to enable better health and treatment outcomes. By ensuring the safety and appropriate use of medicines, we empower healthcare decisions that positively impact patients’ lives.


What You Will Achieve

The Senior Associate – DMM strengthens clinical data oversight through ownership, control, and visibility of clinical records. You will be critical in processing, reviewing, and managing clinical data to ensure accuracy and consistency. By collaborating across teams and leveraging data management systems, you will ensure timely deliverables that support clinical and therapeutic goals.


How You Will Achieve It

  • Data Management: Serve as the Data Manager for one or more clinical trials, overseeing all Data Monitoring and Management (DMM) activities.
  • Operational Excellence: Collaborate with partners and colleagues to ensure standards application and data review processes are operationally excellent.
  • Data Validation: Develop data cleaning reports and validate data quality as specified in the Data Management Plan.
  • Continuous Improvement: Document lessons learned during studies and share them to facilitate cross-study improvements.
  • Collaboration: Build strong relationships with local and global Subject Matter Experts (SMEs) and leverage their expertise to proactively resolve issues.
  • Testing & Reviews: Set up and test data review listings to ensure completeness and accuracy.

Qualifications

Must-Have

  • Bachelor’s Degree.
  • 3+ years of experience in data management processes and principles.
  • Experience with web-based data management systems.
  • Working knowledge of electronic document management systems.
  • Familiarity with International Conference on Harmonization (ICH) guidelines and Good Clinical Practices (GCP).
  • Thorough understanding of clinical study management and regulatory operations.
  • Ability to manage tasks, time, and priorities effectively.
  • Strong verbal and written communication skills, adaptable to diverse audiences.

Nice-to-Have

  • Master’s Degree.
  • Relevant experience in the pharmaceutical industry.
  • Proficiency with data visualization tools.
  • Experience with commercial clinical data management systems or electronic data capture (EDC) products.
  • Awareness of regulatory requirements and relevant data standards.

Work Location Assignment

On Premise


Equal Employment Opportunity

Pfizer is committed to diversity and inclusion and complies with all applicable equal employment opportunity legislation.

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