GFR CDC/ Sr Clinical Data Coordinators (Based in Bloemfontein or Centurion)

Quintiles (NYSE: Q) is the world’s largest provider of biopharmaceutical development and commercial outsourcing services with a network of more than 30,000 employees conducting business in approximately 100 countries. We helped develop or commercialize all of 2013’s top-100 best-selling drugs on the market.

Quintiles applies the breadth and depth of our service offerings along with extensive therapeutic, scientific and analytics expertise to help our customers navigate an increasingly complex healthcare environment as they seek to improve efficiency and effectiveness in the delivery of better healthcare outcomes. To learn more about Quintiles, please visit www.quintiles.com


Provide solid core and some comprehensive data management expertise to Data Management to provide efficient, quality

data management products that meet customer needs. Provide leadership either in the role of the Data Operations Coordinator (DOC), or in a leadership role in a specific DM task (e.g. lead of a task on a megatrial, coder, and database designer for technologies that don’t require extensive programming expertise).


Serve as Data Operations Coordinator (DOC) for one or two global studies with fewer than 10 operations staff (excludes

DE), or serve in a leadership role to a specific DM Task.

Manage delivery of projects through full data management study life-cycle (with minimal guidance).

With guidance from DTL or Manager, manage project timelines and quality; determine resource needs; identify out-of scope work.

Serve as Data Operations Coordinator or Data Team Lead (with guidance).

Perform comprehensive data management tasks including data review, writing and resolving data clarifications.

Perform database designer activities for technologies not requiring extensive programming.

Perform comprehensive quality control procedures.

Independently bring project solutions to the CDM team.

Solve issues through using the global issue escalation/communication plan.

Consult with Standards Group for process issues; communicate ideas for process improvement.

Assist in developing and implementing new technology.

Understand and comply with core operating procedures and working instructions.

Meet objectives as assigned.

Develop and maintain good communications and working relationships with CDM team.

Interact with CDM team members to negotiate timelines and responsibilities.


Good understanding of clinical drug development process

Background in Medical Terminology, Pharmacology, Anatomy, and Physiology

Excellent organizational, communication, and data management skills (detail oriented)

Ability to establish and maintain effective working relationships with coworkers, managers and clients


Bachelor’s degree, or educational equivalence, in clinical, biological, or mathematical sciences or related field or nursing

qualification with 1 year clinical trials experience in function similar to DM; or equivalent combination of education,

training and experience

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