IQVIA

Clinical Trial Coordinator (Oncology)

IQVIA is looking for a Clinical Trial Coordinator in experience in Oncology based in Rosebank, Gauteng. The successful candidate will be responsible for providing expertise in the design, implementation, management and evaluation of study protocols and research tools; supporting the development of new funding proposals; analysing qualitative and/or quantitative data; and leading scientific papers, reports and policy briefs for our client in Rosebank. Strong support to existing biomedical projects and should have capability to lead an area of research.

Qualifications:

  • - Degree in Biological Science (BSC), Pharmacy or other health-related discipline preferred, Nursing or other relevant qualification/experience is an advantage.
  • - Strong knowledge in Medical, Biomedical or Epidemiology research (Oncology).
  • - 2-3 Years’ experience in a similar role.

Key Duties:

  • - Conduct and facilitate specific start-up activities such as feasibility, site identification, pre-qualification, Site Regulatory Package (SRP) review and approval, Clinical Site Agreements (CSA) and Informed Consent (ICF) customization and negotiation (when required), and application, preparation and submission, in accordance with relevant regulations, SOPs, and study specific procedures.
  • - Client focused approach to work
  • - Screenings of Study Feasibilities
  • - Enrolment Visits
  • - Patient Eligibility
  • - Advanced problem-solving skills
  • - Strong computer skills including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word
  • - Site Initiation Visits
  • - Ability to interact professionally with external customers.
  • - Advanced ability to manage multiple and varied tasks with enthusiasm
  • - Informed Consent discussions with patient
  • - Screening visits
  • - Treatment visits
  • - Follow-up visits
  • - Planning and coordinating blood tests, scans and other results
  • - Adverse Events, Serious adverse events and Concomitant Medication
  • - Entering information on eCRF systems, responding to queries
  • - Payment of travel money
  • - Keeping track of trial invoicing and payments
  • - Assisting monitors with site visits

Key Skills:

  • Flexible attitude with respect to work assignments and new learning
  • Willingness to work in a matrix and virtual team environment and to value the importance of teamwork
  • Strong interpersonal, verbal, and written communication skills
  • Sense of urgency in completing assigned tasks
  • Effective time management in order to meet daily metrics, team objectives, and department goals
  • Ability to work independently with little oversight and to proactively seek guidance when necessary
  • Strong ability to influence and negotiate resolutions and outcomes with sites

Should you meet the criteria, please apply on Linkedin. No emailed applications will be accepted.

If you have any questions, please do email Thapi Mokose

Please note: If you have not received a response in 3 weeks, please consider your application unsuccessful.

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