Clinical Data Manager, Sarah Cannon Research Institute - Nashville, TN
Sarah Cannon Research Institute -Nashville - Nashville, TN

This job posting is no longer available on HCA Inc. Find similar jobs: Clinical Data Manager jobs - Sarah Cannon Research Institute jobs

GENERAL SUMMARY OF DUTIES: This position is responsible for clinical data management of SCRI clinical trials. This includes all data management activities from protocol review to the final data deliverable to the sponsor. The Clinical Data Manager supports data management project activities according to pre-defined timelines and ensures timely completion of those projects. This position must clearly demonstrate the ability to manage multiple projects with different sponsors and timeline demands.

RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:
  • Develops Data Management Plans for multiple protocols simultaneously
  • Ensures all processes are compliant with SOPs
  • Collaborates with clinical project manager to determine study timelines and milestones
  • Represents Data Management on project core teams
  • Team Leader responsible for collaborating with Data Quality staff to ensure high quality database on time and on budget
  • Manages Data Management project budgets
  • Responsible for CRF/database design and implementation, including specifications, testing and production
  • Responsible for producing CRF completion guidelines
  • Main point of contact for all data management issues for assigned projects
  • Represents SCRI to external sponsors for project specific activities
  • Provides technical direction to Clinical Data Analysts
  • Ensures the data management processes are compliant with SOPs
  • Maintains project documentation relevant to data management activities
  • Keeps management abreast of issues and progress on all assigned projects
  • Mentors and coaches new and/or junior data management staff
  • Contributes to internal process development and improvement
  • Other duties as assigned
Qualifications

KNOWLEDGE, SKILLS & ABILITIES - This position requires the following minimal requirements:

  • Ability to manage multiple protocols and participate on multiple project teams simultaneously
  • Strong attention to detail
  • Excellent communication skills, oral, written and presentation
  • Excellent organizational skills
  • Excellent problem solving skills
  • Knowledge of GCP/ICH guidelines
EDUCATION

  • Qualified candidates will have a BA/BS or equivalent experience
EXPERIENCE

  • 3 years of Clinical Data Management or other relevant experience or equivalent experience.
  • Demonstrated ability to work collaboratively with project teams to deliver a clean database
  • Demonstrated ability to anticipate data quality issues during design and planning stages
  • Demonstrated ability to offer solutions to data handling issues
  • Demonstrated ability to overcome obstacles and consistently meet deadlines
  • Demonstrated ability to work collaboratively with sponsors and provide customer service

HCA Inc - 19 months ago - save job - block
Recommended Jobs
Clinical Trials Manager for Sarah Cannon - Na...
Sarah Cannon - Nashville, TN
HCA Inc - 10 days ago

Clinical Trials Specialist for Sarah Cannon R...
Sarah Cannon - Nashville, TN
HCA Inc - 10 days ago

Clinical Research Coordinator- Cardiac - Sara...
Sarah Cannon - Nashville, TN
HCA Inc - 30+ days ago