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BACKGROUND
My client is a highly successful, international biotechnology firm engaged in the discovery and development of medical treatment products. This position is in the San Francisco area.DUTIES/RESPONSIBILITIES
- Plan, design and implement clinical research projects
- Supervise data collection and be the contact with Investigators
- Ensure compliance with protocols
- Approve CRFs
- Implement monitoring plan
- Supervise CROs
REQUIREMENTS
- BS in Science, Nursing or equivalent
- 5 + years in clinical research as a CRA with a pharma company or CRO
- Ability to manage studies from Phase I to large scale Phase II/III trials
- Knowledge of clinical study design and FDA/GCP regulations
- Strong communication and supervisory skills, including coaching/teaching CRAs and CROs.
PREFERENCES
Advanced degree preferredLOCALE
The company is headquartered in California, in the SAN FRANCISCO BAY area.SALARY & COMPENSATION
THIS IS A $100K OPPORTUNITY + full fringe benefits + bonus + stock optionsHOW TO APPLY
Send your resume/CV, including position title and code to:
MichelleM[at]LifeScienceRecruiters.com
Michelle Mauro
LIFE SCIENCE RECRUITERS
973-601-3500
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Discussion forums: Opportunity: SENIOR CLINICAL RESEARCH ASSOCIATE (Code CRA-1)--San Francisco, CA (US)
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Comment
How I can become a member of International Bi
Submitted by
Nobody
;
posted on
Sunday, November 28, 2004
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How I can become a member of International Biopharmaceutical Association?
http://www.ibpassociation.org/
should I take a training with
http://www.kriger.com/
for this?
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