Senior Clinical Research Associate I (Melbourne- home …, Adelaide
Senior Clinical Research Associate I (Melbourne- home …, Adelaide
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Adelaide, Australia
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Posted: yesterday
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Description
Senior Clinical Research Associate I (Melbourne
- Home Based) Updated: Yesterday Location: Adelaide, SA, Australia Job ID: Job Responsibilities
- Perform site qualification, site initiation, interim monitoring, site management and close‑out visits (onsite or remotely), ensuring regulatory, ICH‑GCP and/or Valuable Pharmacoepidemiology Practices (GPP) and protocol compliance.
- Evaluate overall performance of site and site staff, provide recommendations on site‑specific actions, and communicate/escalate serious issues to the project team and develop action plans.
- Maintain a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs / processes. Qualifications
- Bachelor’s degree or College/University degree in Life Sciences or an equivalent qualification.
- Minimum of 4 years of independent clinical monitoring experience.
- Excellent communication and interpersonal skills with internal and external stakeholders.
- Good time management skills and demonstrated critical thinking.
- Full working rights in Australia or New Zealand (Open to Visa Transfer Sponsorship in AUS). The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and responsibilities as needed. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate. #J-18808-Ljbffr Apply on Kit Job: kitjobau.com/job/3ruk0l
- Home Based) Updated: Yesterday Location: Adelaide, SA, Australia Job ID: Job Responsibilities
- Perform site qualification, site initiation, interim monitoring, site management and close‑out visits (onsite or remotely), ensuring regulatory, ICH‑GCP and/or Valuable Pharmacoepidemiology Practices (GPP) and protocol compliance.
- Evaluate overall performance of site and site staff, provide recommendations on site‑specific actions, and communicate/escalate serious issues to the project team and develop action plans.
- Maintain a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs / processes. Qualifications
- Bachelor’s degree or College/University degree in Life Sciences or an equivalent qualification.
- Minimum of 4 years of independent clinical monitoring experience.
- Excellent communication and interpersonal skills with internal and external stakeholders.
- Good time management skills and demonstrated critical thinking.
- Full working rights in Australia or New Zealand (Open to Visa Transfer Sponsorship in AUS). The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and responsibilities as needed. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations when appropriate. #J-18808-Ljbffr Apply on Kit Job: kitjobau.com/job/3ruk0l
Highlights
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Company nameSyneos Health
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Job positionSenior Clinical Research Associate I (Melbourne- home based) (Adelaide)
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