Associate Data Manager
PfizerAbout the role
Job Summary:
The Senior Associate, Data Management will play a critical role in ensuring the integrity, accuracy, and consistency of clinical trial data. This position involves managing data collection, processing, and quality control activities for clinical research studies. The Senior Associate will collaborate with cross-functional teams to support data management activities and ensure compliance with regulatory requirements and company standards.
Key Responsibilities:
- Coordinate and execute study configuration activities, including mapping technical specifications and ensuring readiness for sample receipt and testing.
- Support the end-to-end data lifecycle for clinical lab testing, including data reconciliation, quality control (QC) checks, and exception handling
- Collaborate with cross-functional teams to ensure timely and accurate data delivery and study setup.
- Perform data validation and integrity checks, ensuring compliance with regulatory standards, GCP, and internal SOPs.
- Support the development and maintenance of study database setup documents and data transfer specifications.
- Participate in the continuous improvement of DMSO processes, including documentation updates, SOP reviews, and system enhancements.
- Serve as a liaison between internal stakeholders and external partners (e.g., CROs) for data agreement execution and secure data transfer coordination.
Required Qualifications:
- Bachelor's degree in Life Sciences, Data Science, or a related field.
- Strong understanding of clinical trial processes and regulatory requirements.
- Excellent attention to detail and problem-solving skills.
- Strong communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Proven ability to troubleshoot data issues, manage competing priorities, and adapt to evolving project needs in a fast-paced environment
Preferred Qualifications:
- Proficiency in LIMS (Laboratory Information Management Systems) applications
- Experience in a pharmaceutical or CRO environment.
Work Environment:
- Hybrid work environment. Minimum 2.5 days onsite required per week
- Collaborative and dynamic team setting.
- Opportunities for professional development and growth.
Work Location Assignment: Hybrid
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gen
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s