Associate Manager CDM Study Lead

Sorry, this job was removed at 08:16 p.m. (CST) on Thursday, May 15, 2025
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3 Locations
In-Office or Remote
97K-158K Annually
Biotech • Pharmaceutical
The Role

Associate Manager, Clinical Data Management (CDM) collaborates with vendor Project Managers and Clinical Data Managers to ensure Data Management functions comply with regulations and study protocols. This role involves preparing the Data Management Plan (DMP) according to company SOPs and Regeneron's data standards, leading data management activities for assigned studies.

As an Associate Manager, a typical day might include the following:

  • Serve as the primary DM study lead for clinical study teams and external partners for small or non-complex studies, or support larger studies within a given TA. Oversee all DM activities from study start-up to archiving.

  • Provide expertise in data management, support eCRF and database design, and ensure data quality.

  • Oversee data quality review procedures, data acceptance, and manage data transfers with CROs.

  • Document and oversee 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.

  • Lead 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.

This role might be for you if you have:

  • Excellent interpersonal, oral, and written communication skills.

  • Effective time management and ability to adapt in a fast-paced environment.

  • Strong understanding of cross-functional activities and proven problem-solving capabilities.

To be considered for this role, you must have:

  • Bachelor's degree in Mathematics, Science, or related field.

  • Certified Clinical Data Manager (CCDM) preferred.

  • Minimum of 6+ years of clinical data management experience in biotechnology, pharmaceutical, or health-related industry.

  • Strong understanding of applicable regulations, including 21 CFR Part 11, ICH-GCP Guidelines, and CDISC standards.

  • Proven leadership in data processing environments and robust knowledge of DM processes.

  • Strong problem-solving, project management, and communication skills.

  • Ability to work effectively in a virtual team environment and manage multiple tasks.

    Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

    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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

    For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions.  For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

    Please note that certain background checks will form part of the recruitment process.  Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

    Salary Range (annually)

    $96,700.00 - $157,700.00

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    The Company
    HQ: New York, New York
    15,000 Employees
    Year Founded: 1988

    What We Do

    At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.

    Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media.

    An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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