FARMOVS Vacancies

The following positions are currently available:

Job Title: Project Manager

Closing Date: 17 September 2021

Job Purpose:

To manage the necessary activities and communication to deliver successful outputs from a central point, delivering a satisfactory study outcome according to the expectations of the Sponsor involved.  To take responsibility for the project management of clinical trials, preparation and co-ordination of trial site, investigator, sponsor and vendor relationship.  Undertake the full range of duties relevant to the preparation and ongoing management of assigned clinical trials and be committed to ensuring that performance meets and or exceeds both the business and personal goals/objectives.

Job Posting Qualifications:

  • Relevant experience within the pharmaceutical or CRO environment would be an advantage.
  • A degree/diploma in Science with biomedical-related subjects is advantageous

All applications to be forwarded to

Job Title: Senior Regulatory Specialist

Closing Date: 30 September 2021

Job Purpose: 

  • The Senior Regulatory Specialist supports site start up activities, from feasibility, contracting, to site activation.
  • Coordinate collection, compilation and prepare materials for submission to regulatory agencies. Manages distribution, storage and tracking and retrieval of information pertinent to the regulatory process, including the regulatory submissions process.
  • May author and publish regulatory submissions (electronic and paper format) as required. Respond to requests from local and global regulatory agencies. Assist with the research, analysis and communication of information pertaining to the appropriate regulatory pathway for awarded clinical trials. Provides regulatory direction to clinical study managers, project managers and study monitors (CRAs) as a core team member. Evaluate risk of proposed regulatory strategies; may offer solutions. Independently communicates with regulatory and governmental agencies to develop a strategic partnership. Establishes relationships with many customers; may meet face to face without rest of team to discuss regulatory issues and present lessons learned. Adopts a proactive and flexible approach to resolve any issues
  • May manage meetings with Regulatory Agencies; May be assigned as Reviewer and/or Approver for Regulatory standard operating procedures or cross-functional standard operating procedures owned by other divisions
  • May support global regulatory or technical initiatives or act as a regional representative on a cross-functional initiative

Job Posting Qualifications:

  • A minimum of 3 years of experience in a similar role
  • A minimum of a Bachelor’s degree required; concentration in clinical or life sciences
  • A combination of education and experience may be considered

All applications to be forwarded to

Please contact us for any HR related queries:

Sandra Gregory (Manager, Human Resources)
+27 51 410 3078

Lee-Anne Reineke
+27 51 410 3253

The FARMOVS team offers the full spectrum of clinical research services and comprises 160 full-time employees with extensive experience and expertise