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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 preferred

LOCALE

The company is headquartered in California, in the SAN FRANCISCO BAY area.

SALARY & COMPENSATION

THIS IS A $100K OPPORTUNITY + full fringe benefits + bonus + stock options

HOW TO APPLY

Send your resume/CV, including position title and code to:

MichelleM[at]LifeScienceRecruiters.com

Michelle Mauro
LIFE SCIENCE RECRUITERS
973-601-3500

Discussion forums: Opportunity: SENIOR CLINICAL RESEARCH ASSOCIATE (Code CRA-1)--San Francisco, CA (US)

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How I can become a member of International Bi

Submitted by Nobody; posted on Sunday, November 28, 2004

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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How I can become a member of International Bi

Submitted by Nobody; posted on Sunday, November 28, 2004

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?