Full-time
Temporary-Clinical Data Manager
Competitive
Bachelor?s degree in mathematics, Science, or a related fieldHealthcarePosted 22d ago
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Role overview
Job type
Salary
Competitive
Sector
Posted
22 days ago
Job description
Responsibilities
Serve as the primary data management contact for assigned studies, representing the function on project teams and partnering with CROs
Coordinate and lead clinical data management activities in line with company SOPs, policies, and regulatory requirements
Monitor CRO data clean-up from study start-up through data archiving to protect data quality and integrity
Coordinate medical coding, data validation checks, and database snapshots, and provide data for analysis
Create and maintain study documentation, including the Data Management Manual, CRF completion guidelines, and validation specifications
Design and modify CRFs, and initiate and approve the build, testing, and validation of clinical databases
Prepare and distribute project status reports to project teams and management
Lead the DM team in ensuring databases are validated and ready for transfer and analysis, while supporting standardization of outsourcing partner processes
Preferred
Previous oncology and/or ophthalmology experience preferred
Benefits
Remote work model
Glassdoor
3.7
Develops and commercializes biopharmaceutical medicines for serious diseases.
Tarrytown, New York, USA
http://www.regeneron.com
Distribution of Different Job Fields Receiving Sponsorship
80
Represents job field similar to this job
Engineering and Development
Management and Executive
Customer Service and Support
Product Management
Legal and Compliance
Accounting and Finance
Sales
Human Resources
Trends of Total Sponsorships
*2026
(291)
2025
(157)
2024
(128)
2023
2022
(137)
2021
(104)
2020
Qualifications
Bachelor?s degree in mathematics, Science, or a related field
3 years of clinical data management experience in biotechnology, pharmaceutical, or a health-related industry
Ability to coordinate and manage CRO data managers and project teams to ensure work follows policies and procedures
Strong understanding of data management processes, database validation, and regulatory compliance
Excellent collaboration, organization, and communication skills
Previous oncology and/or ophthalmology experience preferred
Required skills
Clinical Data Management, CRO Management, Database Validation, Regulatory Compliance, Oncology, Ophthalmology
Preferred skills
Previous oncology and/or ophthalmology experience preferred
Experience
3+ years
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