Reference: MID015957-TB-1 Interested in Quality Assurance in the Medical Field? Want to pursue a career in line with Audits, Document Management and Compliance with Regulatory Bodies? Apply here Minimum requirements: Tertiary Qualification in a Medical-Related Field Matric is a minimum requirement 1
Reference: MID015957-TB-1 Interested in Quality Assurance in the Medical Field? Want to pursue a career in line with Audits, Document Management and Compliance with Regulatory Bodies? Apply here Minimum requirements: Tertiary Qualification in a Medical-Related Field Matric is a minimum requirement 1
is on the lookout for a detail-oriented SHE Administrator to join their dynamic team. This role may develop
company based in Midrand is looking for a QA / RA Administrator for a contract position until February 2025 provide report timeously for Management Review. ASSISTANCE WITH SAHPRA APPLICATIONS Support in processes Operating Procedures and Quality Documents. General administrative duties including archiving, filing, issue of
company based in Midrand is looking for a QA / RA Administrator for a contract position until February 2025 provide report timeously for Management Review. ASSISTANCE WITH SAHPRA APPLICATIONS Support in processes Operating Procedures and Quality Documents. General administrative duties including archiving, filing, issue of
is on the lookout for a detail-oriented SHE Administrator to join their dynamic team. This role may develop
Client in the Fund administration sector is seeking an experienced candidate with 1 year Verification verification checks Perform bank verifications Assist with any ad hoc duties or projects assigned by
Client in the Fund administration sector is seeking an experienced candidate with 1 year Verification verification checks Perform bank verifications Assist with any ad hoc duties or projects assigned by
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as
clinical trial to ensure protocol and GCP compliance Assist study team with efficient study start-up, conduct missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory correctly per protocol within the scope of practice Assist in patient recruitment, screening, and enrolment visits/audits or similar Manage procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job training where necessary Assist the team with ad hoc assignments and duties as