Manager, Clinical Data Management

Regeneron Pharmaceuticals, Inc., Uxbridge, Greater London

Manager, Clinical Data Management

£181100

Regeneron Pharmaceuticals, Inc., Uxbridge, Greater London

  • Full time
  • Permanent
  • Remote working

Posted today, 14 Nov | Get your application in now to be one of the first to apply.

Closing date: Closing date not specified

job Ref: d5ebc4fd68344d7f8b5d374171707949

Full Job Description

We are looking for a Clinical Data Manager who will serve as the DM study lead and point of contact for clinical study teams and external partners, (e.g, external data vendors and CROs) for multiple trials (phases 1-3) within a given Therapeutic Area (TA). You will oversee DM activities across all stages of the trial from study start-up through archiving to achieve data management results within the assigned drug assets and contributes to department-level goals to ensure timely completion within project budget guidelines and adhering to all applicable policies and procedures. As a Clinical Data Manager, a typical day might include 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.
  • Supervise the implementation and execution of procedures for data quality review and data acceptance prior to data analyses and/or database lock.
  • Lead 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. Lead scheduling and time constrains across multiple projects.
  • Prepare recommendations for new or improved processes for data management and data flow
  • May oversee small program with limited number of studies
  • Accountable for providing comprehensive program level oversight of SDMs to ensure consistency and compliance of program level standards, track milestones/deliverables, escalate and follow to resolution as necessary, and communicate program level updates to SDMs
  • Perform & document the oversight of CRO data management activities for assigned studies.

    Strong problem solving, project management, and communication skills required.
  • Ability to work effectively with and motivate virtual teams in matrix environment.
  • Strong understanding of cross functional activities.
  • Proven problem-solving skills.
  • Strong ability to manage multiple and varied tasks with enthusiasm, prioritize workload with attention to detail.
  • Effective time management to meet objectives.
  • Excellent interpersonal, verbal, and written communication skills.
  • Ability to adjust in a fast-paced environment.
  • To be considered for this role, you must have a Bachelor degree in Mathematics, Science or a related field, minimum of 10 or more years of clinical data management experience in biotech, pharmaceutical or health related industry is required. Certified Clinical Data Manager (CCDM). Demonstrated broad knowledge of all applicable regulations including 21 CFR Part 11, ICH-GCP Guidelines and CDISC standards for data collections. #LI-remote