Position - Temp -Data Manager
Pay Range - $80/Hr -$90/Hr
Location - Remote
Duration - 12 months
 

SUMMARY: 
Works collaboratively with vendor Project Managers and Clinical Data Managers to assure that Data Management 
functions are performed in compliance with regulations and according to study protocol and the Study Data Management 
Manual (DMM). Works with involved parties to assure that DMM is prepared according to company SOPs and in 
compliance with Regeneron’s data standards. Coordinates, leads and performs clinical data management activities for 
assigned studies in accordance with Regeneron’s SOPs and policies and practices.
SCOPE:
N/A
JOB RESPONSIBILITIES: 
• Serves as primary DM contact for assigned studies, including representation on project teams and 
working with CROs performing data management tasks for assigned study. 
• Coordinates, leads and performs clinical data management activities for assigned studies in accordance 
with Regeneron’s SOPs and policies and practices including, not limited to: 
o Monitors data clean-up process performed by CROs from study start-up through data archiving.
o Provides data for analysis.
o Coordinates activities including: medical coding; data validation checks and database snapshot.
• Prepares and distributes project status reports to project team and management.
• Functions as DM team leader responsible for ensuring databases are validated and ready for transfer 
and/or analyses in accordance with Regeneron SOPs.
• Creates and maintains project documentation, including, but not limited to, Data Management Manual, 
CRF Completion Guidelines and validation specifications, and work instructions for assigned projects. 
Designs and modifies CRF.
• Responsible for the initiation and approval of the building, testing and validation of clinical databases, 
subsequent changes in clinical databases and data validation activities.
• Contributes to upkeep Regeneron DM outsourcing strategies and long-term relationships with 
outsourcing partners with objective of ensuring data quality and efficiencies through data and process 
standardization. 
• Works with study team and coordinates all data management functions. Manages coordination of CRO 
data manager and project team to ensure that tasks are performed according to policies and procedures. 
JOB REQUIREMENTS: 
Education
• Bachelor’s degree in Mathematics, Science or a related field, along with 3 or more years of clinical data 
management experience in biotechnology, pharmaceutical or health related industry. 
Experience
• 3 – 5 Years
• Previous oncology and/or ophthalmology experience a plusPlease copy and paste the desired job description for this role here. If you need a copy of an existing job description please reach out to TA or work with your HR Business Partner to develop one for a new role.

This is a contract position at Regeneron with Magnit Global being the Employer.

To do our best work we need different viewpoints.  Therefore, we celebrate diversity and embrace inclusion. As an equal opportunity employer, we are dedicated to building a team that represents a variety of backgrounds, perspectives, and skills.  We strive to ensure that we maintain a positive and enriching work environment for all.

W2 only, no third-party solicitation