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Need Experienced Clinical Research Coordinator
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Comments (7)

FLORA Research in Fort Lauderdale, Florida

36 months ago

Looking for a full-time contract clinical research coordinator for a Hematology Oncology Practice. This position will involve organization and management of 3 offices in the West Palm Beach area to coordinate and conduct clinical research trials. This is a regular daytime position, and the hours will be flexible depending on patient scheduling.
Proficient in word processing (Word) and comfort with spreadsheets (Excel).
- Organizational, time management, and leadership skills, along with excellent attention to detail, are required
- The ability to work independently with minimal supervision is required
- Degree in nursing is preferred
- Oncology experience or Research experience is needed

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Susan Driscoll-Bannister in Fort Lauderdale, Florida

36 months ago

June 16,2009

To whom it may concern:

I have over twenty years of clinical research at experience at major academic medical centers.I have been a IRB member as well as having my certification in clinical research through ACRP since 2000.

I would be happy to send you my resume for your review.

I look forward to hearing from you regarding this interesting position.
Sincerely
Susan Driscoll-Bannister

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Susan Driscoll-Bannister in Fort Lauderdale, Florida

36 months ago

My e-mail address is susanbannister@yahoo.com

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Judy Fayter in Strathmere, New Jersey

35 months ago

Certified clinical research coordinator, SoCRA. 20 years experience coordinating oncology cooperative group research to include all aspects, ie: recruitment, informed consent process, CRF's, AE & SAE reporting, audits, etc. ECOG, GOG, SWOG, ACRIN.
Experience with IRB submission and GCP.
Pharmaceutical research exp.

Available for home-based contract.

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lauren glenn in Budd Lake, New Jersey

30 months ago

Judy Fayter in Strathmere, New Jersey said: Certified clinical research coordinator, SoCRA. 20 years experience coordinating oncology cooperative group research to include all aspects, ie: recruitment, informed consent process, CRF's, AE & SAE reporting, audits, etc. ECOG, GOG, SWOG, ACRIN.
Experience with IRB submission and GCP.
Pharmaceutical research exp.

Available for home-based contract.

Hello Judy

Is this position still available?

Regards

Lauren Glenn

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Judy in Avalon, New Jersey

30 months ago

lauren glenn in Budd Lake, New Jersey said: Hello Judy

Is this position still available?

Regards

Lauren Glenn

I listed a brief summary of my expertise, I am searching for a CRC position.

Judy

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irene in Saskatoon, Saskatchewan

29 months ago

is this position still available

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