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Manager, Clinical Data Scientist, Clinical Data Sciences

10+ years
Not Disclosed
10 Aug. 7, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Why Patients Need You

At Pfizer Worldwide Medical and Safety, we are dedicated to bridging the gap between evidence-based medical decision-making and practical healthcare solutions. Our mission is to empower healthcare professionals with the knowledge and tools needed for safe and effective use of medicines, thereby enhancing patient outcomes. By providing scientifically sound frameworks, unbiased expertise, and identifying data gaps, we contribute to better health and treatment decisions.

What You Will Achieve

Your role will be crucial in overseeing clinical data management, ensuring accurate and timely data processing, and maintaining high standards of data integrity. You will be responsible for organizing and validating clinical data from various sources, ensuring it reaches the relevant medical departments and stakeholders. As a Manager, you will guide operational teams, plan resources, and propose improvements for processes and products. Your leadership will facilitate cross-team collaboration and advance new methodologies.

How You Will Achieve It

  • Project Management: Lead or co-lead projects, manage time effectively to meet objectives, and plan resource needs for division-wide projects.
  • Data Oversight: Ensure compliance with Standard Operating Procedures (SOPs) and best practices, promote efficient and high-quality processes, and manage all Data Monitoring and Management (DMM) activities for clinical trials.
  • Technical Expertise: Serve as a Clinical Data Scientist and Trial Lead, providing technical support and business process guidance for data visualization, reporting tools, and technology systems.
  • Operational Excellence: Collaborate with partners to ensure standards are applied, data acquisition is effective, and data management activities are handled with integrity.
  • Central Monitoring: Perform central monitoring tasks, review system outputs, suggest actions for data signal management, and coordinate with study teams to resolve issues.
  • Communication: Develop and execute communication plans to engage customer populations effectively.

Qualifications

Must-Have:

  • Bachelor’s Degree
  • 10+ years of experience in the pharmaceutical industry or health information management
  • Strong understanding of all phases of clinical trials and ability to assess study requirements from protocol reviews
  • Knowledge of clinical research regulations, including FDA and ICH-GCP
  • Excellent project and risk management skills
  • Strong verbal and written communication skills, with the ability to handle multiple tasks
  • Proficiency in Windows Environment and its applications

Nice-to-Have:

  • Master’s Degree
  • Experience with Contract Research Organizations (CROs) and vendor oversight
  • Familiarity with commercial clinical data management systems and EDC products

Work Location Assignment: On Premise

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