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Sr. Clinical Research Associate- Oncology
You will be involved in the submission of protocol, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested. Approximately 65% travel overall can be expected, primarily regional but will include national as needed.
uccessful candidates will possess:
· Bachelor's degree in a life science or related discipline OR RN/LPN with 4 years related experience.
· 3 years of onsite monitoring experience
· Experienced in oncology/immunotherapy protocols
· Strong understanding of ICH GCP Compliance
· Ability to travel 65-70% of the month
To apply for this position, please visit
BioTech FYI Center