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Senior Associate, Data Manager, Clinical Data Sciences

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

About Pfizer:

Pfizer is dedicated to improving global health by providing evidence-based medical decision support and ensuring the safe and effective use of medicines for patients. Through innovative solutions and global collaboration, Pfizer’s Worldwide Medical and Safety teams contribute significantly to advancing healthcare and treatment outcomes.

Job Overview:

The Senior Associate, Clinical Data Management will play a crucial role in managing, processing, and reviewing clinical data across multiple therapeutic areas. This role will focus on ensuring the accuracy, timeliness, and consistency of clinical data and collaborating with internal and external stakeholders to drive operational excellence. The Senior Associate will also contribute to the creation of data management plans, validation activities, and data cleaning reports.

Key Responsibilities:

  • Data Management: Manage and monitor clinical data for one or more clinical trials, assuming responsibility for Data Monitoring and Management (DMM) activities.
  • Collaboration: Work closely with cross-functional teams, including global subject matter experts (SMEs), to ensure data management standards and quality.
  • Data Review: Set up and test data review listings to verify the completeness and quality of clinical data.
  • Operational Excellence: Ensure operational excellence in DMM deliverables, including data validation and cleaning reports.
  • Issue Resolution: Proactively identify and address issues related to data management, ensuring consistency and accuracy.
  • Knowledge Sharing: Document and share lessons learned from studies to facilitate cross-study learning and improve processes.

Qualifications:

Must-Have:

  • Bachelor's Degree (required).
  • 3+ years of experience in clinical data management or related fields.
  • Strong knowledge of data management processes and principles.
  • Experience with web-based data management systems.
  • Proficient knowledge of electronic document management systems.
  • Familiarity with International Conference on Harmonization (ICH) and Good Clinical Practices (GCP).
  • Thorough understanding of clinical study management and regulatory operations.
  • Strong organizational skills with the ability to manage tasks and prioritize effectively.
  • Effective verbal and written communication skills, with the ability to adapt communication to different audiences.

Nice-to-Have:

  • Master's Degree in a related field.
  • Relevant pharmaceutical industry experience.
  • Experience using data visualization tools.
  • Experience with commercial clinical data management systems and/or EDC products.
  • Awareness of regulatory requirements and relevant data standards.

Why Pfizer?

Pfizer is committed to creating an inclusive, diverse workplace and offers opportunities to work on global projects that impact patients worldwide. You will be part of a team that is dedicated to improving healthcare outcomes and empowering medical decision-making through innovative data management.

Equal Opportunity Employment:

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

Work Location: On Premise

Job Posting ID: #LI-PFE


For more information or to apply, visit Pfizer’s careers site.