As a Clinical Research Associate II / SCRA you will be the link between investigational site and sponsor to ensure the clinical trials are delivered to the appropriate timelines and resources.
- Liaise between sites and different sponsors
- Follow a relevant study plan and organise, prepare, conduct and follow up routine monitoring and closing out of visits.
- Motivating and training investigators and site staff to ensure that obligations are met and in line with study timelines.
- Adhere to ICH - GCP and any other regulatory guidelines and requirements including adverse events and serious adverse event reporting.
- You will be degree qualified with a Bachelors or higher degree in a health/science related field
- You will have 2-3+ Years independent monitoring experience within ANZ
- Strong Verbal and written communication and Interpersonal skills
- Working knowledge of ICH-GCP Guidelines
- Excellent organisational skills – ability to organise, take initiative and follow-up independently
Send resume to tehreem@jobs-n-jobs.com or tehreemshah279@gmail.com
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