Clinical Data Manager - Bloemfontein based (R1083563) in Bloemfontein, South Africa at IQVIA™

Date Posted: 7/7/2019

Job Snapshot

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

RESPONSIBILITIES  

  • Serve as Data Team Lead (DTL) / customer site lead for multiple large global studies / programme of global studies.
  • Provide leadership and senior support to DTLs on multiple large global studies / programme of global studies.
  • Act as the main overall point of contact for internal and external customers for programme / multiple projects.
  • Manage relationship with a customer on a CDM site level.
  • Manage delivery of multiple projects / programmes through the full data management study life-cycle independently.
  • Independent management of programme / project timelines, quality, resources, SOW (scope of work) / budgets.
  • Lead CDM customer negotiations on complex timeline, budgetary and other issues.
  • May serve as Project Manager for single service data management projects.
  • Manage comprehensive data management tasks pertaining to the documented project specifications.
  • Manage comprehensive quality control procedures.
  • Provide data management expertise and process improvement to CDM management.
  • Mentor other team members in training and developing data management expertise.
  • Independently bring project solutions to the CDM team and the CDM Department.
  • Manage a focus team or a best practice team.
  • Manage the development and implementation of new technology/tool.
  • Present at professional conferences and/or publish articles in professional journals.
  • Provide CDM with technical expertise.
  • Provide review and expert opinion in developing, revising, and maintaining core operating procedures and working instructions.
  • eet objectives as assigned.
  • Develop and maintain good communications and working relationships with CDM and project teams.

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES    

  • Advanced knowledge of the data management process / systems and experience in specialized data management skills

  • Comprehensive understanding of clinical drug development process

  • Outstanding communication and organizational skills (detail oriented)

  • Proven leadership skills

  • Ability to establish and maintain effective working relationships with co-workers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • Bachelor’s degree, or educational equivalence, in clinical, biological or mathematical sciences, or related field, or nursing qualification:, 7 years’ experience in clinical trials within a similar function, including proven competence in managing delivery of multiple global projects / programs independently through full data management study life-cycle, including large trials >1000 patients; also including experience in handling complex customer negotiations and bid defence meetings; or equivalent combination of education, training and experience

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.



Job ID: R1083563

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