Reference: NFR004229-IZ-1 If you are a tax specialist looking to expand on their tax knowledge, then Description: If you are a skilled corporate tax specialist looking for a new and exciting opportunity, then
Johannesburg Metro, Johannesburg
Embark on an exhilarating journey as a Payroll Tax Specialist with this esteemed company. We're on the hunt
Are you ready to supercharge your career in the dynamic world of Commercial Insurance? Do you thrive on building strong client relationships, providing expert advice, and securing the best coverage solutions? If so, we have the perfect opportunity for you Our client is a leading player in insurance
Are you ready to supercharge your career in the dynamic world of Commercial Insurance? Do you thrive on building strong client relationships, providing expert advice, and securing the best coverage solutions? If so, we have the perfect opportunity for you Our client is a leading player in insurance
Reference: NFR004229-IZ-1 If you are a tax specialist looking to expand on their tax knowledge, then Description: If you are a skilled corporate tax specialist looking for a new and exciting opportunity, then
for a suitably qualified Fire Detection Scada Specialist to offer technical specialised support on products
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and and regulatory authorities regarding notifiable trial events Prepare for and manage participant visits minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education, work
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and and regulatory authorities regarding notifiable trial events Prepare for and manage participant visits minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education, work