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Regeneron
The Head of Clinical Data Management (CDM) is fully accountable for all clinical data management activities in support of the clinical pipeline. This includes, but is not limited to, execution and ownership of the CDM operating model, oversight of internal staff and external CDM partners, and cross-functional leadership for the delivery of high quality and reliable clinical data to enable internal decision making, regulatory approval, and market acceptance.
The incumbent interacts with senior level management, partners with external vendors, collaboration partners and provides cross functional strategic direction and is accountable for building and managing a team across functions to identify risks and opportunities as well as innovative approaches to clinical data management. The Head of Clinical Data Management is critical to the success of our clinical trials and the integrity of data that supports regulatory submissions and decision-making.
In this role, a typical day might include:
Establishing and driving global data management strategy related to resourcing, technologies and processes to increase efficiency, innovation and data quality.
Defining and executing the vision and long-term goals for the department.
Leading the global data management function to provide data collection, cleaning, and integration expertise in support of global development projects including all disease areas and business units; ensure functional strategy supports the portfolio priorities while also remaining close to the business and portfolio
Accountability for meeting annual goals, objectives and deliverables for both internal and external Clinical Data Management (CDM) partners.
As the business owner of the Clinical Scientific Data Lake, develop, implement, and oversee the clinical data model and standards in support of the global portfolio.
Building efficient and compliant processes to support regulatory inspections
Driving the organization towards high quality, efficiency, and standards
Ability to effectively structure an organization to manage the anticipated growth in the global product pipeline.
This role might be for you if have expertise leading the following areas:
Data Management and Data Integrity Oversight:
Ensure timely and high-quality data management deliverables supporting the Regeneron clinical study portfolio
Responsible for Sponsor Oversight of Data Management deliverables and activities performed by Strategic Partners, CROs, and 3rd Party Vendors
Lead implementation of clinical data management best practices (e.g., cross-functional data review, emerging data collection technologies, etc.)
Prepare for and facilitate regulatory audits and inspections, ensuring readiness and compliance.
Data Operations and Vendor Management:
Accountable for resourcing algorithms that enable appropriate staffing
Serve as Subject Matter Expert and data-specific liaison for Process, Training and Compliance and other internal initiatives/projects
Design and implement clinical data management standard processes, ensuring engagement with key partners on critical processes such as cross-functional data review; issue escalation, etc.
Build and maintain relationship with vendors for the purpose of providing outsourcing solutions, functional solutions and staff augmentation services, as well as building new and/or improved data management capabilities
Metrics, Analytics and Reporting:
Lead development of Clinical Data Management metrics, represent CDM function in projects and initiatives related to the reporting and analytics capabilities, including but not limited to Dashboards, Portfolio level performance and productivity and predictive analytics/reporting
To be considered for this opportunity, you must have the following:
Minimum Bachelor’s Degree
17+ years of clinical data management experience in a pharmaceutical or biotech setting
12+ years of functional leadership
10+ years people management, leadership and mentoring experience
May require up to 25% travel
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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)
