Lead Data Manager

DR. VINCE CLINICAL RESEARCH, P.A.
United States
about 1 month ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Working hours
Regular working hours
Job source

Tech stack

Coherent Remote File System (CRFS) Data Validation Data Dictionary Data Management

Job description

POSITION SUMMARY: The Lead Data Manager is responsible for overseeing the data management processes across clinical trials, ensuring the quality, integrity, and compliance of clinical trial data. This position involves leading the protocol assigned data management team members, collaborating with cross-functional teams, and playing a pivotal role in the success of clinical studies., * Oversee the design, implementation, and maintenance of the selected EDC system or systems

  • Lead the creation and review of data management documentation (e.g., CRFs, data dictionaries, data validation plans)
  • Mentor any applicable data management team members, providing guidance and training as needed
  • Ensure protocol assigned team members are meeting deadlines, following SOPs, and maintaining high standards for data quality
  • Work closely with clinical operations, biostatistics, clinical monitoring, and regulatory teams to ensure data management activities align with study goals and timelines
  • Track data management progress and provide regular updates to study teams and management

Provide feedback on draft protocols, TLFs, and Statistical Analysis Plans as needed * Other data management services as required

Requirements

  • High school diploma or equivalent
  • Strong communication skills with the ability to manage multiple projects simultaneously
  • Capable of completing deadlines on time and regulate priorities in a fast-paced environment
  • Knowledge of CDISC (CDASH, SDTM)
  • Great organizational skills with the ability to multi-task
  • Proficient in various EDC systems, 5+ years of data management experience in the Pharmaceutical and/or CRO setting * MedDRA and WHODrug coding experience preferred, but not required.

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