Study Coordinator
1 week ago
Duties/Pligte
- Coordinating study patient visits;
- Monitoring oncology patients and providing all vitals and observations;
- Appropriate clinical trials source document management and capturing it into relevant electronic records;
- Liaising with the pharmacies regarding clinical trial medications;
- Administering all relevant trial medication;
- Coordinating academic research administration and clinical studies;
- Collecting and sending information requested by patients and clinicians;
- Data entry and database management;
- Assisting with the ethics submissions for clinical trials and academic research;
- Acting as communications liaison between co-investigators, research assistants, administrators, patients / study participants;
- Liaising with pharma trial managers and providing all requested reports;
- Assisting with the preparation of documentation for SAHPRA.
Job Requirements/Pos Vereistes
- Diploma in Nursing;
- Current registration with the South African Nursing Council (SANC);
- A good verbal and written command of English and one or more official South African language;
- Proficient in the use of Word and Excel, and knowledge of Microsoft Access and Teams;
- Nursing skills, including knowledge of the safe administration of intravenous, intramuscular, subcutaneous and oral medication;
- Knowledge of or experience in clinical trials and clinical research as study coordinator;
- Knowledge of or experience in data management;
- Working hours need to be flexible for patient flow.
Recommendation/Aanbeveling
- Familiar with Stellenbosch University's online ethics submission process;
- Licensed to administer intravenous chemotherapy;
- GCP certification.
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