Clinical Study Coordinator jobs in Stellenbosch

Duties/Pligte Duties:Facilitating learning and training (including teaching, mentoring and guiding) of undergraduate students in theoretical and practical aspects of Speech-Language and Hearing Therapy;Supervising undergraduate students during practical activities in relevant sites on the distributed training platform;- Planning, organising and facilitating learning opportunities;- Effectively...

Faculty- Department- Cape Peninsula University of Technology -> Health & Wellness Sciences -> Nursing- Campus/ Location- Bellville Campus - Bellville, Cape Town, WC ZA (Primary)- Job Type- Contract- Occupational Function- Support / Admin- Number of Positions- 10- Annual Salary Package (incl. Medical Aid rate based on principal member only)- To be confirmed- Advert Closing Date- 17/9/2025- Job...

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 Position: The position, which is primarily based at an...

Job Overview Responsible for study build & design, edit specifications, system configurations and is accountable for associated study design components. This role will collaborate with various stakeholders- DTL, Programmer, Validation Team, vendors, statisticians, and client representatives. In addition to project deliveries, the role also would be responsible for the project financials from...

We provide meaningful careers that connect people with purpose. We are united by a common purpose of providing the best and safest care; and by our shared values of Care, Truth, Participation, Compassion and Dignity. Netcare invites you to be part of our journey. Role Summary: The Professional Nurse/Clinical Nurse is a professional who remains responsible for the assessment, planning and...

Duties/PligteCoordinating clinical research study projects, ensuring effective and efficient implementation and compliance with regulatory stipulations and study protocols;- Maintaining, coordinating and monitoring project plans, project schedules, work hours, resources, equipment, information, budgets and expenditures;- Assessing project risks and issues, and providing solutions where...

IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward. Data Team Lead,...

Duties/Pligte - Assisting with the administration of the Practical Legal Training (PLT) final year, clinical legal education module; - Organising student duty sessions; - Serving as liaison between students and the Clinic's professional staff; - Teaching and mentoring students in clinical components; - Supervising and mentoring students during their interactions with clients; - Assessing student...

Bellville, South Africa | Full time | Home-based | R Job available in additional locations Site Activation Coordinator / Senior Site Activation Coordinator Country Site Activation – CSA Entry-Level & Senior Opportunities Available South Africa Shape the Future of Patient Health At IQVIA, we're united by one mission: to improve patient outcomes around the world. Our Global Site Activation...

Duties/Pligte Duties will include, but will not be limited to: - For the global collaboration and capacity strengthening component, the incumbent will play in a key role in coordinating a suite of capacity strengthening activities aimed at co-producing and using pre-clinical and early phase living systematic reviews, simultaneously. The coordinator will identify LMIC postgraduate students and...

Duties/Pligte The duties of the SU-UIC coordinator will include the following: - Supporting the Senior Coordinator/Programme Manager with liaising with the Examinations Councils. - Coordinating the delivery of contracted services. - Providing support in setting up, and the subsequent functioning and coordination of, the SU-UIC committees, external moderators and specialists. - Arranging...

Duties/PligtePerforming real time data quality checks of informed consent forms and paper and/or electronic source documents across all research studies;- - Data query logging, following up and managing query resolutions for all IRG clinical studies;- - Data capturing;- - Coordinating the preparation and maintenance of participant hard copy documents and files for all IRG clinical studies;- -...

Duties/PligteWorking closely with the BMRI clinical team, data manager(s) and study statistician(s) to ensure that study procedures and results are accurately reported in the study database (REDCap), in order to facilitate efficient and accurate analysis;- Monitoring eCRFs for compliance with the specific protocol, Good Clinical Practice (GCP), sponsor and regulatory requirements;- Monitoring...

Duties/PligteBeing situated at a study site to recruit and consent study participants, including in a busy and occasionally crowded space;- Meeting recruitment targets and managing multiple studies through simultaneous enrolment;- Assisting with tracing patients;- Working closely and maintaining good relations with other research nurses, city clinic staff, field staff, study clinician and...

Duties/Pligte - Providing clinical paediatric care and support to children enrolled in the MIS-C study; - Assessing children with febrile illnesses and conducting clinical exams; - Assisting with phlebotomies and other medical procedures, including collection of respiratory samples for virus analysis; - Working with a multidisciplinary team that includes laboratory and clinical staff; -...

Duties/Pligte - Providing leadership for the research team. - Developing and maintaining Standard Operating Procedures and research forms. - Ensuring that ethical requirements are fulfilled. - Interacting with the principal investigator and other investigators to ensure the fulfilment of project goals. - Interacting with study auditors. - Assisting with the planning of the project to achieve the...

Duties/PligteEssential prospective cohort duties:- Conducting screening and enrolling participants, explaining research procedures, obtaining informed consent, and conducting interviews with participants;- Coordinating specimen collection and specimen processing;- Performing data collection and data entry. Maintaining clear, concise, accurate, and legible records;- Scheduling study visits and...

Duties/PligteBeing situated at a study site to recruit and consent study participants, including in a busy and occasionally crowded space;-- Meeting recruitment targets and managing multiple studies through simultaneous enrolment;-- Assisting with tracing patients;-- Working closely and maintaining good relations with other research nurses, city clinic staff, field staff, the study clinician and...

Duties/Pligte- Performing all study activities according to the protocols and SOPs;- Recruiting, consenting and enrolling study participants;- Collecting quantitative (survey) data electronically (using tablets) and through headcounts;- Collecting specimens (tongue swabs and sputum) from participants;- Collecting qualitative data through focus groups and in-depth interviews (using an audio...

Duties/Pligte- Assisting the lead pharmacist in all activities in the FAMCRU pharmacy;- Reviewing all protocols for active studies;- Assisting with procedures, medications (dosage, frequency, administration), inclusion/exclusion criteria and amendments;- Maintaining drug storage, record-keeping and inventory control;- Attending monitoring/audit visits;- Keeping abreast of Institutional Review...