Senior Associate, Data Manager, Clinical Data Sciences

3+ years

Not Disclosed

Chennai

10 Dec. 23, 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

Senior Associate, Clinical Data Management - Pfizer

About the Opportunity:

Pfizer Worldwide Medical and Safety teams are essential in connecting evidence-based, medical decision support to ensure safe and effective treatment outcomes. As a Senior Associate in Clinical Data Management, you will play a crucial role in processing, reviewing, and managing clinical data to ensure accurate, timely, and consistent data delivery to clinical teams and stakeholders. Your expertise will be key in strengthening clinical data oversight, providing critical insights, and contributing to the advancement of life-saving therapies.

What You Will Achieve:

In your role as a Senior Associate, Clinical Data Management, you will:

Lead Data Management Activities: Take responsibility for managing Data Monitoring and Management (DMM) activities for clinical trials, ensuring data integrity, quality, and compliance with the Data Management Plan.
Data Review and Validation: Collaborate with cross-functional teams to review and validate data, identifying areas for improvement and proactively resolving data-related issues.
Operational Excellence: Drive operational excellence by ensuring the application of standards, conducting data cleaning, and developing reports in support of the data review plan.
Collaboration & Relationship Building: Foster strong relationships with subject matter experts (SMEs) globally and locally, leveraging their expertise to address issues and create solutions.
Knowledge Sharing: Document lessons learned during studies and share insights with other teams to drive continuous improvement across clinical trials.
Project Management: Effectively manage your time and workload to meet deadlines, ensuring smooth project execution and successful deliverables.

Qualifications:

Must-Have:

Education: Bachelor’s Degree in a relevant field.
Experience: 3+ years of experience in clinical data management.
Knowledge: Strong understanding of data management processes, Good Clinical Practices (GCP), and regulatory requirements.
Systems Experience: Familiarity with web-based data management systems and electronic document management systems.
Communication Skills: Strong verbal and written communication abilities, with the ability to adapt communication to diverse audiences.
Time Management: Ability to effectively manage tasks, prioritize work, and meet deadlines.

Nice-to-Have:

Education: Master’s Degree.
Experience: Relevant pharmaceutical industry experience.
Technical Skills: Experience with data visualization tools and commercial clinical data management systems or EDC products.
Regulatory Awareness: Knowledge of regulatory requirements and data standards.

Work Location:

On Premise

Why Pfizer:

Pfizer is committed to being an equal opportunity employer and complies with all relevant employment legislation in every jurisdiction we operate. By joining Pfizer, you will help contribute to new milestones in medicine and the improvement of patient outcomes globally.

#LI-PFE

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Senior Associate, Data Manager, Clinical Data Sciences

Job Description

Senior Associate, Clinical Data Management - Pfizer

What You Will Achieve:

Qualifications:

Must-Have:

Nice-to-Have:

Work Location:

Why Pfizer:

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