Please note that we are an immigration company and do charge a facilitation fee. We are accredited by OMARA, a branch of the Department of Immigration and Border Protection in Australia. For a Free Eligibility assessment please apply online, contact 27 21 201 1551 or follow the link to complete a fr
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
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
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:
with the performance of clinical trial-related duties in line with Good Clinical Practice (GCP) standards areas: Conduct Quality Control activities for clinical trials, assist with regulatory communications qualification A recognized Quality Control Course (for clinical trials) Computer literacy at a higher level including experience in a clinical trial environment At least 5 years experience working in clinical trials At least
with the performance of clinical trial-related duties in line with Good Clinical Practice (GCP) standards areas: Conduct Quality Control activities for clinical trials, assist with regulatory communications qualification A recognized Quality Control Course (for clinical trials) Computer literacy at a higher level including experience in a clinical trial environment At least 5 years experience working in clinical trials At least
with the performance of clinical trial-related duties in line with Good Clinical Practice (GCP) standards ul>
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application the public health sector Experience managing a clinical trial Good data management skills Able to work
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application the public health sector Experience managing a clinical trial Good data management skills Able to work
through public health-focused epidemiological, clinical, and basic science research and innovation