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US-CA-Glendale: Research Associate in Biotech

Date: 28-Jun-2011
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Research Associate in Biotech

-Performs appropriate psychometric and efficacy testing according to study protocol.

-Receives authorized sign-off to verify accuracy of all study participant visits.

-Prepares/monitors study supplies and stock levels in clinic/hospital.

-Labels, inventories and sends plasma samples.

-Problem solves study participant issues as they arise.

-Assumes appropriate role with study participants and caregivers.

-Attends and assists with start-up and flowsheet meetings.

-Completes Case Report Forms (CRF) in a timely manner.

-Assures quality and accuracy of source and CRF documentation.

-Complies with Quality Management (QM) department guidelines and performs corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.

-Assists with Monitor visits (i.e., room set up, etc.).

-Follows medical records procedure.

-Ensures basic study participant safety is provided.

-Maintains accurate accountability for petty cash.

-Identifies issues that need Sponsor approval and brings these to the attention of the CRC.

-Exhibits professional demeanor at all times in external interactions with Sponsors/Sponsor Representatives.

-Maintains supportive, flexible manner internally with management, coworkers/team members.

-Maintains and updates knowledge of Clinical Operating Guidelines and their proper application.

-All other duties as assigned.

Education -BS, BA in a related field or equivalent work experience. -BSN, RN, foreign MD or Masters Degree a plus.

Language Skills -English or English/Japanese

Experience: Minimum Work Experience -Prior clinical research experience, floor nursing, and/or psychiatric experience a plus.

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Thank you,
BioTech FYI Center