Covance Inc

Clinical Data Manager II (BB-AEA5B)

Found in: Neuvoo Bulk CA

Description:
JOB DESCRIPTION

Job Overview:

Covance is seeking candidates for a Clinical Data Manager II. The Clinical Data Manager II can be remotely (home-based) anywhere within the United States or Canada. 

  • Serve as the technical leader on all data management aspects for project(s) including start-up, maintenance, and completion activities.
  • Develop [Global] Data Management Plans and Quality Management (QM) Plans that will deliver accurate, timely, consistent, and quality clinical data.
  • Identify and implement solutions to project data management issues and concerns, including proactive prevention strategies based on metrics and forecasts.
  • Serve as the project and client liaison including management and provision of project specific data management status, cycle time, and productivity metrics.
  • Coordinate and participate in the development of the clinical data model and/or database design and annotate the CRF (eCFR) according to these specifications.
  • Review data acquisition conventions and data review guidelines / diagnostic specifications consistent with the clinical data model, [statistical] analysis plans, and CRF (eCRF) completion / monitoring conventions.
  • Coordinate the development and testing of data management system edit / data validation checks (diagnostics) and special listings / procedures used as tools for the data review and discrepancy management activities.
  • Advanced planning and risk management for projects (issue escalation, resource management).
  • Support recruitment of new data management candidates.
  • Interact and collaborate with other project and specialty team members (clinical, programming, statistics, CDM technical support, drug safety, etc.) to support the set-up, maintenance, and closure of the data management aspects of the project to ensure consistent, cohesive data handling and quality.
  • Supervise, mentor and evaluate performance of data managers in the location and aide in staff development, career development, interpersonal skills, and achievement of competency standards.
  • Support the technical mentoring of data review staff in regional locations and aide in staff development, career development, interpersonal skills, and achievement of competency standards.
  • Oversee the technical performance of the data review project staff on achieving client satisfaction through delivery of quality data, on-time and on-budget.
  • Maintain technical data management competencies via participation in internal and external training seminars.
  • Ensure project staff are trained and adhere to project-specific, global, standardized data management processes.
  • Identify areas for process and efficiency improvement and implement solutions on assigned projects.
  • Support achievement of project revenue and operating margin for data management activities to agreed targets.
  • Develop and maintain strategic client relationships and receive client satisfaction surveys and implement appropriate action plans as necessary.
  • Support business development for data management time and cost estimates and prepare and present to potential clients on global data management capabilities.
  • Review literature and research technologies / procedures for improving global data management practices.

    • Education/Qualifications:

  • University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
  • Additional relevant work experience will be considered in lieu of formal qualifications.
  • Broad knowledge of drug development process.
  • Understanding of global clinical development budgets and relationship to productivity targets.
  • Thorough knowledge of effective clinical data management practices.
  • Thorough knowledge of time and cost estimate development and pricing strategies.
  • Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing.

    • Experience:

  • Minimum six (6) years relevant work experience in data management with approximately three (3) years technical supervisory experience to include data management, clinical operations, knowledge of several therapeutic areas.
  • Demonstrated skill for technical management of staff exceeding 10 employees.
  • Financial management of gross revenues in excess of $500K per year.
  • Excellent oral and written communication and presentation skills.
  • In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operations.
  • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
  • Demonstrated ability to lead by example teams on project strategies and achievement of department goals, objectives, and initiatives and to encourage team members to seek solutions.
  • Demonstrated managerial and interpersonal skills.

    • #LI-REMOTE

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