Manager, Clinical Data Manager Study Lead

Build our future together:   The  Manager   CDM,   provides oversight of lead Data Manager(s) on assigned clinical data management studies in specific therapeutic areas to assure proper planning and execution for data management deliverables that meet Regeneron standards and within timelines.   Assists   in the development of SOPs, Working Practice, Data Management Plan, and other data management standards.    When & where:   Work Location:   Remote   25% Travel may be   required   Discover your role:   Serve as the DM study lead and the primary point of contact for clinical study teams and external partners, (e.g., external data vendors and CROs) for 1 or more complex studies within a given TA. Oversee all DM activities across all stages of the trial from study start-up through archiving. To include but not limited to the following:   Provide   a high level   of   expertise   in data management to support clinical studies.   Provide clear verbal or written information and hands-on support to project team members and to   CROs related to eCRF and database design, data quality, and reporting of database / data quality status.    Oversee the implementation and execution of procedures for data quality review and data acceptance prior to data   analyses   and/or database lock.   Manage data transfers with CROs and third-party data sources, SAE/AE   reconciliation   and MedDRA/WHO-DD coding.   Support the transfer, locking, and archiving of study databases. Manage scheduling and time   constrains   across multiple projects.   Prepare recommendations for new or improved processes for data management and data flow.   Perform & document the oversight of CRO data management activities for assigned studies:   Ensure the design, implementation and maintenance of electronic case report   forms,   clinical trial database and electronic edit checks are performed according to SOPs and   WIs.   Identify   data quality, CRO performance, documentation, process execution gaps   and is   accountable for resolution.   Document DM sponsor oversight activities from protocol review through study close-out.   Escalate and   follow to   resolution   as necessary.   Review and approve study documentation for assigned studies, (including, but not limited to):    Data Management Plan or equivalent ( includes:   Data Review, Reconciliation and Cleaning,   Coding,SAE   Recon, Local Lab Handling activities for CRF and non-CRF data)   Case Report Form and Completion Guidelines   Validation   specifications     and   data transfer specifications   This role requires:   Bachelor Degree   or equivalent experience in Mathematics,   Science   or a related field with at least   7   or more years of clinical data management experience   in biotechnology, pharmaceutical or health related   industry    Perform quality review and inspection readiness tasks to meet quarterly Inspection Readiness   Review (IRR) compliance    Follow   through on   gaps until resolution,   escalating   as necessary.   Lead/oversee all data management deliverables for assigned studies:   Ensure deliverable timelines are developed according to the business   need   and program   objectives .   Ensure   snapshot/lock plans are developed and collaborate with the CST for review and approval.   Ensure regular status updates with metrics are provided to CST.   Provide program level input   to &   monitor   deliverable timelines.   Monitor data quality and assess progress of data issue remediation on an ongoing basis.   Identify   risks, propose mitigations, proactively escalate operational or DM vendor or DM CRO issues.   May provide limited program level support for a small program with limited number of studies   Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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, and 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