CRAs - Join Covance and receive a $5000 Sign On Bonus!
Meet the CRA hiring team at the ACRP conference - email [email removed].
Set yourself up for SUCCESS with Early Clinical Development!
Now is the time to join our growing business where you have supportive management and a cohesive team.
At Covance, you are not just a number. We value you and your hard work...we want you to succeed.
URGENT Need for Oncology Monitors! Calling all Experienced Clinical Research Associates / CRAs / Monitors ...
Senior Regional Clinical Research Associate
Identifies potential investigators, contract research organizations and outside vendors. Collects required documentation for review by Project Manager to make a selection decision.
Conducts site visits pre-study, at study initiation, at regular intervals during the study and at study closeout.
Prepares a variety of reports and letters in accordance with study SOPs and industry standards.
Collects, reviews and processes regulatory documents. Ensures ...
A dynamic and growing CRO is looking for a regional CRA. Responsibilities include but are not limited to: performing monitoring visits including site qualification, initiation, monitoring and close-out visits; maintaining regular contact with study site to ensure protocol/GCP compliance; participating in Investigator meetings and other study training meetings as required; preparing for and participating in Sponsor and FDA audits.
Proven success in monitoring clinical ...
Regional Clinical Research Associate
The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of ...
* Demonstrated management/supervisor related experience.
* Excellent leadership and management abilities.
* Strong aptitude in the art and science of quality, CMC, and preclinical procedures and methods.
* Good working knowledge and understanding of ICH Guidelines for Good Clinical Practice and Title 21 of the Code of Federal Regulations.
* Strong understanding of international regulations regarding clinical research (EMEA, PMDA, Health Canada, etc.)
* Experience working closely with ...
Relocation assistance available
Bioinformatics scientists provide bioinformatics and statistical analysis support for biomarker discovery, IVD product development and CMI tumor molecular profiling service.
· Develop and maintain statistical analytical tools and bioinformatics pipelines.
· Conduct analysis and develop innovative algorithms on biomarker discovery and clinical ...
Jun 4 -
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