Clinical Research Coordinator: Consent

Essential Requirements Grade 12 / National Senior Certificate or Equivalent Counselling qualification or counselling experience GCP qualification 5+ years of clinical research workers experience inclusive of clinical trials experience Experience with electronic consents and regular interfacing with e-data bases Ability to engage with the community and...

Essential Requirements Grade 12 / National Senior Certificate or Equivalent Counselling qualification or counselling experience GCP qualification 5 years of clinical research workers experience inclusive of clinical trials experience Experience with electronic consents and regular interfacing with e-data bases Ability to engage with the community and present...

**Overall Purpose of the Position**: The Clinical Trial Assistant I (CTA I) plays a crucial role in supporting the efficient operation of clinical research activities by providing comprehensive administrative and data management assistance. The Clinical Trial Assistant I ensures the smooth execution of daily study tasks, maintains accurate study...

**About the Company**: TASK is a South African headquartered, multinational clinical research institute that conducts clinical trials to determine the treatment effects of novel medicinal products or devices in healthcare and offers services in conducting complex clinical trials in a wide variety of therapeutic areas. **Overall Purpose of the...

Minimum Requirements: Undergraduate qualification in a health-related discipline At least 2 years experience in a research environment /or clinical experience Computer literacy (MS office) including database competency An understanding of publication processes and procedures advantageous Good Clinical Practice Certification (advantageous) Computer Literacy...

**Coordinate** all clinical study activities between International Sponsors, Doctors, Nursing staff, and the patient. Collect reports and manage all **clinical data** to the sponsor company. **One year experience in clinical trials is a requirement** **Preparation for study** - Meet with sponsor delegates to discuss all aspects of the site and requirements...

A leading medical research institute in Cape Town is seeking a Study Coordinator to manage clinical research activities. Candidates should possess a relevant healthcare qualification and 2-5 years of clinical research experience. The role includes screening participants, managing study logs, and performing clinical procedures. The position is contract-based,...

SUMMARY:Under the general supervision of the Principal Investigator(s), assists in acquisition and analysis of patient information for multiple clinical research projects. Interviews patients to gather information, prepares and maintains study record, enters data via computer, performs statistical analyses of resultant data. Participates in...

A leading research institution in Cape Town seeks a Clinical Research Coordinator to manage study participants and conduct various clinical procedures. The ideal candidate should hold a relevant qualification and have 1-2 years of clinical research experience. This fixed-term role involves numerous responsibilities, including liaising with clinical staff and...

Minimum Requirements:Undergraduate qualification in a health-related disciplineAt least 2 years experience in a research environment /or clinical experienceComputer literacy (MS office) including database competencyAn understanding of publication processes and procedures advantageousGood Clinical Practice Certification (advantageous)Computer...