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
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?
Submitted by
Sudheshna
;
posted on
Wednesday, October 20, 2010
There is a Job Opening For Biology Scientists (in vivo) in SSF,CA.we are looking for people with good lab techniques and zeal to deliver their talent.You can upload your resume at makroscientific.com.
You can contact me at sudheshnasowrab@yahoo.com for any concerns and clarifications.
Good Day..
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