Careers

We bridge the capacity building gap in Africa by providing site management systems and operational support to research investigator sites in the conduct of clinical research and clinical trials through our world-class dedicate research sites (DRS) and affiliated sites.

A career at CRISMO offers stability, secure employment, a friendly and supportive culture, and the opportunity to learn, grow and be part of our ambition to make a difference.

Main purpose of the job:

CRISMO invites qualified and experienced Medical Officers (Research Investigators) to apply for a sessional or full-time position. The successful candidate will support the Principal Investigator on ongoing clinical research studies. Responsibilities include conducting study procedures according to protocol, ensuring participant safety, monitoring and documenting adverse events and ensuring compliance with Good Clinical Practice (GCP) standards.

Location:

CRISMO Research Centre – Bertha Gxowa Hospital

and

CRISMO Bloemfontein Research Centre – Universitas Private Hospital

Should you be interested in this role, please send a cover letter and supporting documents to the following email boitumelo@crismo.co.za. 

Instructions for sending the email:

  • Supporting Document (CV, Cover Letter and Qualifications with SA GCP certificate, HPCSA, MPS and Ethics in Health Research Training including TREE)
  • Use the Job Title on the Subject Line

CRISMO complies to POPI Act, by sharing your documents you give CRISMO permission to process your data and storing.

Key Performance areas:

  • Conduct study procedures in compliance with study protocols and GCP guidelines.
  • Screening and enrolment of study participants according to the inclusion/exclusion criteria.
  • Completing Case Report Forms (CRFs) as per study requirements.
  • Reviewing and signing all laboratory results.
  • Ensuring the randomization process is correctly implemented.
  • Supervising and managing medical treatments and proceduresof all participants in the study.
  • Monitor and document participant safety, including the identification and management of adverse events and serious adverse events (SAEs).
  • Report safety data to relevant stakeholders including the sponsor and regulatory bodies.
  • Assisting the monitors during monitoring visits to make sure that all queries are responded to.
  • Responding to Data Correction/Clarification Forms (DCFs) on time.
  • Fostering relationship with local clinic staff including medical practitioners.
  • Supervising pharmacy activities.
  • Managing treatment adherence program for all participants of the study, including retention planning.
  • Provide study details to the participants and obtain signed informed consent.
  • Participate in medical writing, publications and feasibility studies review as needed.

Required minimum education and training

  • A Medical Degree (MBBCH)
  • Valid SA GCP training certificate
  • Ethics in Health Research Certificate
  • TREE Modules Certificate

 Required minimum work experience

  • 2 years minimum experience working in the clinical research environment and sub investigator experience.

Professional body registration:

  • HPCSA
  • Malpractice Insurance Policy (MPS)

Additional Personal Abilities

  • Ability to manage multiple studies simultaneously in a fast-paced environment.
  • Attention to detail.
  • Sound written and verbal communication skills.
  • Understanding of the ALCOA principles and application
  • Punctual and good time keeping
  • High degree of integrity and trustworthiness
  • Strict compliance to study protocols.
  • Organizational and administrative skills and working with Microsoft Office.
  • Self-motivated with a high regard for work ethic, values and integrity.
  • Display a concern for participants and willingness to respond to participants needs and requirements.