Experienced Clinical Research Associate
2 giorni fa
As a seasoned Senior Clinical Research Associate, you will be responsible for overseeing clinical trials in oncology studies, working closely with investigative sites to ensure compliance with sponsor's procedural documents and international guidelines. Your expertise will be invaluable in assessing site qualification, initiating trials, instructing site personnel, and closing trials.
Key Responsibilities- Assess the qualifications of potential investigative sites and initiate clinical trials accordingly
- Instruct site personnel on proper conduct of clinical trials and close trials at investigative sites
- Review and verify accuracy of clinical trial data collected, either on-site or remotely
- Provide regular site status information to team members and updates trial management tools
To succeed in this role, you will need:
- 4+ years of clinical monitoring experience, preferably in oncology studies
- Strong knowledge of ICH and local regulatory authority regulations regarding drugs
- Excellent leadership skills, with ability to coach and mentor other CRAs
We offer a competitive salary range of $110,000 - $140,000 per annum, depending on experience, as well as various annual leave entitlements, health insurance options, retirement planning benefits, and more.
About KCRKCR is a clinical development solutions provider creating value for emerging biotechnology organizations. As part of the ICON organization, we serve clients globally with key operations hubs in Boston, US, Berlin, Germany, and Warsaw, Poland.
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