Write and edit clinical development documents, including but not limited to, clinical protocols, investigator’s investigator’s brochures, clinical study reports, subject consent forms, integrated safety and efficacy least 3-5 years of industry regulatory writing and clinical medical writing experience The ideal candidate medical, clinical discipline Substantial Oncology experience required Substantial clinical study protocol submissions (clinical study reports) presented to regulatory authorities a plus Understanding of clinical data
South Natal - KZN: The successful candidate will form part of the company's technical division and have
all necessary stationery and material (e.g. pens, forms and brochures) Provide basic and accurate information
products, responding to queries and facilitating clinical discussions. Source new business opportunities
suppliers. • Implementation of discount structure as applicable.
accustomed to working in a corporate environment. Applicants are required to meet the following criteria: and drafting investment reports The successful applicant would be responsible for, but not limited to:
from us within 5 days, please accept that your application was unsuccessful
within the next 2 weeks, please consider your application unsuccessful. Vacancies are advertised on our measures to protect the personal information of applicants and for the purpose of this disclaimer “personal
products, what its main components are and what its applications are on the company products.
or around Ballito Due to the high volume of applications received, only suitable candidates who meet