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Senior Associate, Senior Data Manager

3+ 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: Senior Associate, Clinical Data Management
Company: Pfizer
Location: On Premise


Why Patients Need You:

Pfizer Worldwide Medical and Safety colleagues play a vital role in connecting evidence-based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. By ensuring that our clinical data is scientifically sound and accessible, we help empower healthcare decisions regarding the safe and appropriate use of medicines for patients.


What You Will Achieve:

Your role will be crucial in strengthening the oversight of clinical data by ensuring stronger ownership, control, and visibility. You will process, review, and receive clinical data from both therapeutic groups and internal/external investigators, ensuring that the data is accurate, timely, and consistent. You will help manage data management plans, including data preparation and validation activities, and ensure that all project targets and deliverables are met in a timely manner.

As a Senior Associate, your knowledge and skills will contribute to achieving the team’s objectives. You will leverage communication tools to resolve issues effectively and help establish consensus across teams.


How You Will Achieve It:

  • Manage your time effectively to meet project targets.
  • Serve as the Data Manager for one or more clinical trials, taking responsibility for Data Monitoring and Management (DMM) activities.
  • Collaborate with partners and colleagues to apply standards and develop data cleaning reports to support the data review plan.
  • Set up and test data review listings to verify the quality and completeness of data as specified in the Data Management Plan.
  • Ensure operational excellence in DMM deliverables, ensuring that any lessons learned are documented and shared across study teams.
  • Build strong relationships with global subject matter experts (SMEs) and leverage their expertise to identify and address issues proactively.

Qualifications:

Must-Have:

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

Nice-to-Have:

  • Master’s degree
  • Relevant pharmaceutical industry experience
  • Experience with data visualization tools
  • Proficiency in commercial clinical data management systems and/or EDC products
  • Awareness of regulatory requirements and relevant data standards

Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.


If you're ready to contribute to important advancements in clinical data management, apply today!