CRA Client-Based South Africa
- Employer
- Syneos Health
- Location
- South Africa (ZA)
- Salary
- Competitive
- Start date
- 23 Dec 2020
- Closing date
- 22 Jan 2021
View more
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Clinical Research Associate II
Johannesburg, client-based
Permanent contract
Sponsor-dedicated
Here at Syneos Health we are currently recruiting for a Clinical Research Associate II to be based in office in South Africa and work closely with one of our global pharma clients.
Job Details:
- Conduct all clinical site monitoring activities according to the monitoring plan and in accordance with the study timelines and company objectives. This includes but is not limited to:
Overview the overall activities of site personnel over whom there is no direct authority and motivate/influence them to meet study objectives.
Ensure quality of data submitted from study sites and assures timely submission of data. Train study site personnel on the protocol and applicable regulatory requirements.
- Facilitate Quality Assurance Audit processes as indicated.
- Report monitoring activities and study site conduct accurately and completely.
- Prepare CA and/or EC documentation, ensures submissions and/or notifications are performed as applicable.
- Manage and liaise with appropriate functions to respond to CA and/or EC questions and related follow-up.
- Negotiate investigator/ hospital agreements with stakeholders.
- Use multiple technologies to maintain open and frequent communication with internal & external customers.
The ideal candidate will need the following experience / skills to be considered:
- Minimum of 1-2 years of clinical monitoring.
- Start-up experience will be asset, as well as experience in monitoring oncology studies.
- Current in-depth knowledge and understanding of appropriate therapeutic indications as they relate to the conduct of clinical trials.
- Current in-depth knowledge of regulations governing clinical research, ICH/GCP Guidelines and applicable regulations.
- Good written and verbal communication skills. Written and verbal fluency in English.
- Previous experience with electronic data capture systems is desirable.
We have a comprehensive benefits package and offer highly competitive remuneration.
Join a game-changing company that is reinventing the way therapies are developed and commercialized. Created through the merger of two industry leading companies, INC Research and inVentiv Health, we bring together more than 22,000 clinical and commercial minds to create a better, smarter, faster way to get biopharmaceutical therapies into the hands of patients who need them most.
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