Manager, Clinical Data Management (CDM), Study Lead

Regeneron Pharmaceuticals; Tarrytown (GA); Remote; USD 173,000 - 187,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Manager Clinical Data Management (CDM), Study Lead to guide DM activities from study start-up through archiving for small to mid-size studies, in a given therapeutic area.

You will support eCRF and database design and ensure data quality, coordinating with CROs and internal teams. The role includes data quality reviews, study documentation, and maintaining eTMF, with a chance to act as SME on DM topics and represent DM in study-level forums.

Qualifications

• Bachelor's degree in Mathematics, Pharmaceutical Science, Pharmaceutics or related field and 6 years of clinical data management experience.
• Experience applying regulations (21 CFR Part 11, ICH GCP) to data collection and management.
• Experience coordinating clinical studies and study teams in a regulated environment.
• Ability to evaluate data workflows and propose process improvements.
• Strong written and verbal communication for crossfunctional teams.

Responsibilities

• Lead data management activities from study start-up to archiving.
• Support eCRF and database design; ensure data quality and timely deliverables.
• Review study documentation (DMP, CRF, validation specs) and maintain eTMF.
• Coordinate data transfers with CROs and document data management processes.
• Represent DM in study-level forums; provide SME input and training as needed.
• Identify data quality issues and propose risk mitigations.

Skills

Clinical Data Management

Regulatory compliance

Cross-functional collaboration

GCP 21 CFR Part 11

Education

Bachelor's degree in Mathematics/Pharmaceutical Science/Pharmaceutics or related field

Tools

eCRF systems

CDISC standards

Job description

Manager, Clinical Data Management (CDM), Study Lead (Tarrytown, NY)

Regeneron Pharmaceuticals, Inc. seeks a Manager Clinical Data Management (CDM), Study Lead (Tarrytown, NY) to serve as the primary DM supporting clinical study teams and external partners on small or noncomplex studies or supporting larger studies within a given therapeutic area. Coordinate all DM activities from study start-up to archiving. Provide expertise in data management, support eCRF and database design, and ensure data quality. Perform data quality review procedures, data acceptance, and coordinate data transfers with CROs. Document and support CRO data management activities, ensuring adherence to SOPs and identifying data quality issues. Review and approve study documentation, including DMP, CRF, and validation specifications. Maintain eTMF documentation and perform quality reviews to ensure inspection readiness. Responsible for data management deliverables, ensuring timelines align with business needs and objectives. Monitor data quality, assess data issue progress, and propose risk mitigations. May act as a Subject Matter Expert (SME) for specific topics and provide training. Represent DM in study-level forums and meetings. Telecommuting permitted.

SALARY RANGE: $172,994.00 - $187,400.00 per year

Job Requirements:

Requires a Bachelor’s degree in Mathematics, Pharmaceutical Science, Pharmaceutics or related field and 6 years of clinical data management experience in biotechnology, pharmaceutical, or health-related industry. Must have experience with: Applying applicable regulations, including 21 CFR Part 11, ICH GCP Guidelines, and CDISC standards, to clinical data collection and management activities; Supporting and coordinating clinical studies and study teams within a regulated data processing environment; Applying data management processes and industry best practices across the clinical data lifecycle, including data collection, validation, and delivery; Evaluating existing data management workflows and recommending process improvements to meet study and organizational objectives; Resolving complex data related issues by analyzing requirements, identifying root causes, and implementing compliant solutions; Preparing and delivering written documentation and verbal communications for crossfunctional clinical study teams; and Collaborating with crossfunctional, geographically distributed study teams in a matrixed environment.

Does this sound like you? We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role:

• annual bonuses or other incentive plans
• equity awards
• pension or retirement benefits
• 401(k) company match
• health and wellness programs
• fitness centers
• insurance benefits (e.g. medical, dental, vision, life and disability)
• paid time off
• family support benefits

For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.