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Senior Associate, Data Manager, Clinical Data Sciences

3+ years
Not Disclosed
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

Job Title: Senior Associate, Clinical Data Management
Department: Medical
Work Location Assignment: On Premise


Why Patients Need You

At Pfizer, our Worldwide Medical and Safety teams are critical in delivering evidence-based medical support and advancing healthcare decision-making. By ensuring our clinical data is scientifically robust and unbiased, we empower stakeholders to make informed decisions regarding the safe and effective use of our medicines, ultimately benefiting patients globally.


What You Will Achieve

As a Senior Associate, Clinical Data Management, you will play an integral role in processing, reviewing, and managing clinical data. By ensuring data is accurate, timely, and consistent, you will support clinical teams and other departments in meeting critical project deliverables. Your contributions will be key to strengthening data oversight, control, and visibility, furthering Pfizer’s commitment to innovation and patient care.


How You Will Achieve It

  • Manage your time effectively to meet team targets and deliverables.
  • Serve as a Data Manager for one or more clinical trials, taking responsibility for Data Monitoring and Management (DMM) activities.
  • Ensure operational excellence in collaboration with partners and colleagues by applying standards and developing data cleaning reports in alignment with the Data Review Plan.
  • Set up and test data review listings to verify data quality and completeness, as outlined in the Data Management Plan (DMP).
  • Document and share lessons learned during studies to facilitate learning and improvement across teams.
  • Build strong relationships with local and global Subject Matter Experts (SMEs) to address issues proactively and leverage their expertise in areas such as systems and processes.

Qualifications

Must-Have:

  • Bachelor’s Degree.
  • 3+ years of experience in clinical data management or related fields.
  • Demonstrated knowledge of data management processes and principles.
  • Experience with web-based data management systems.
  • Working knowledge of electronic document management systems.
  • Understanding of International Conference on Harmonization (ICH) guidelines, especially Good Clinical Practices (GCP).
  • Strong understanding of clinical study management and regulatory operations.
  • Proven ability to manage tasks, time, and priorities effectively.
  • Excellent verbal and written communication skills, with the ability to adapt communications to diverse audiences.

Nice-to-Have:

  • Master’s Degree.
  • Relevant experience within the pharmaceutical industry.
  • Familiarity with data visualization tools.
  • Proficiency with commercial clinical data management systems and/or Electronic Data Capture (EDC) products.
  • Awareness of regulatory requirements and relevant data standards.

About Pfizer

Purpose:
Pfizer is committed to breakthroughs that transform patient lives. Guided by our core values—courage, joy, equity, and excellence—we lead in innovation and deliver exceptional outcomes globally.

Equal Employment Opportunity:
Pfizer celebrates diversity and inclusivity, fostering a culture that empowers employees and drives excellence in patient care.


Medical
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