Marie Stopes Clinics Jobs in South Africa
Clinical Technologist
Bloemfontein
Are you a skilled Clinical Technologist with expertise in sonars and cath lab procedures? Our esteemed requirements:
- Bachelor's degree in Clinical Technology or related field.
- Experience
share this job on whatsappClinical Operations Associate Remote Work
Hutchinson Centre Research Institute Of South AfricaSouth Africa
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this coordinate and facilitate clinical site specimen processing and clinical testing laboratory projects Division of AIDS or DAIDS contractors. Manage clinical site laboratory supply program including resourcing teams that support the implementation of HVTN clinical trials in Southern Africa. Other duties and assignments
Clinical Lab Operations Qa Associate
Hutchinson Centre Research Institute Of South AfricaSouth Africa
The Clinical Laboratory Operations QA Associate I reports to the Lead Clinical Laboratory Operations Laboratory Operations of specimen processing for HVTN clinical trials across Southern Africa. A person in this coordinate and facilitate clinical site specimen processing and clinical testing laboratory projects Division of AIDS or DAIDS contractors. Manage clinical site laboratory supply program including resourcing teams that support the implementation of HVTN clinical trials in Southern Africa. Other duties and assignments
Pharmacovigilance Physician Centurion
Express Employment Professionals Sa - MidrandCenturion
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
Pharmacovigilance Physician - Centurion Salary Dependent On Experience And Qualification
Express Employment Professionals Sa - MidrandCenturion
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
Medical Technician NEW
South Africa
not applicable CONTRACT
EMAVUNDLENI CLINICAL RESEARCH SITE; CROSSROADS
The Desmond carry out laboratory activities at Emavundleni Clinical Research Site, as well as to ensure that the final of health and safety regulations
Advantageous:
- Clinical trials/research experience
- Tertiary qualification Association Training Certificate (IATA)
- Good Clinical practice (GCP) and Human Subjects Protection
Senior Research Project Manager NEW
East London
Market related engagement activities
Professional Nurse Johannesburg, South Africa NEW
Aj PersonnelJohannesburg
focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development coordinating all aspects of clinical research study activities and ensuring that clinical research projects are attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the experience, and personal abilities: Clinical research experience Excellent clinical skills Driver's license Computer
Study Coordinator (professional Nurse 24 Months Ftc Wits Vida) NEW
Aj PersonnelJohannesburg
focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development coordinating all aspects of clinical research study activities and ensuring that clinical research projects are attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the experience, and personal abilities: Clinical research experience Excellent clinical skills Driver's license Computer
Research Assistant
Guguletu
Market related related research materials
- Certificate in Good Clinical Practice (GCP)
- Experience in qualitative
Share on Facebook
Share on Twitter
Share on Linkedin