Clinical Trial Coordinator - FSP (Johannesburg)

at  Parexel

Register your interest for upcoming Clinical Trial Coordinator positions, office based in Gauteng.
Please provide some basic information and upload your resume. As soon as the role becomes available, we will promptly send you an email invitation to apply officially.
Open to Clinical Trial Assistant, Study Coordinator, Clinical Trial Coordinator, Project Support Associate, ICSM, CRA. or similar. Minimum 1-2 years experience in a similar Clinical Research role gained with CRO, Pharma, or Biotech (academic or hospital or healthcare experience is not a match for this role.)
Everything we do has the potential to impact patient lives, and our Trial Coordinators take their work seriously, demonstrate empathy, and act with heart.

SKILLS AND EDUCATION:

• Minimum 1-2 years experience in a similar Clinical Research role gained with CRO, Pharma,or Biotech (academic or hospital or healthcare experience is not a match for this role.)
• Good understanding of Global, Country/Regional Clinical Research Guidelines.
• Experience in trial and site administration support.
• Regulatory & Site Start-Up experience.
• B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience.
• Effective time management, organizational and interpersonal skills, conflict management.
• Effective communication with external customers (e.g., sites and investigators).
• Able to work independently.

POSITION PURPOSE:

The Clinical Trial Coordinator (CTC) will support the Clinical Research Manager (CRM) and other team members through the life cycle of the study from study start-up to study closure.

PRIMARY DUTIES:

• Trial and site administration and support.
• Regulatory & Site Start Up responsibilities.
• Meeting Planning.