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Duke University Health System

CLINICAL RESEARCH SPECIALIST

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Job Information
Post Date: Today Type: Full time
Start Date:2009-11-17 06:01:22 AM+ Salary:- n/a -
Location: NC - Durham Job Reference: - n/a -
Facility:

Duke University Health System
Job Details
Description
CLINICAL RESEARCH SPECIALIST
400356680
27634BR
Durham
DUKE HOSPITAL
ABMT SUPPORT
First/Day
FULL TIME
4029 CLINICAL RESEARCH SPECIALIST
D2

Occupational Summary

Perform a variety of research, data base and clerical duties of a
routine and technical nature in support of multi-center clinical trials
to ensure adherence to protocols and quality of information received.

Work Performed

Perform a variety of research, data base and clerical duties of a
routine and technical nature in support of multi-center clinical trials
to assist investigators in organizing, gathering and compiling clinical
research data.

Maintain and update site demographics on computer
data base; log forms received and file as appropriate; prepare reports
from data base to include weekly reports and other reports as
requested.

Receive and disseminate study-related regulatory
documents and correspondence from assigned sites; assist in screening
documents for completeness and compliance with protocol and appropriate
regulations; assist in investigating incomplete, inaccurate or missing
documents to ensure accuracy and completeness of data.
Assist in
maintaining communications with sites to provide information, track
documentation and overall progress of clinical trials and adherence to
established guidelines; ensure that study materials and drug kits are
shipped and re-supplied as requested; respond to routine questions
related to study protocol and refer more complex questions to others as
appropriate; document all conversations in the data base.


Communicate regularly with regional data monitors as needed to
provide information before and after visits to participating sites;
review the monitor's post visit reports and follow up on problems
identified as appropriate.

Communicate and coordinate with other
study personnel as required to include data entry and randomization
personnel, pharmacy, laboratories, study sponsors and others as needed
for study implementation and routine problem resolution.

Attend
routine weekly meetings and other meetings related to the clinical
trial; stay abreast of information and any changes to study protocol.


Perform other related duties incidental to the work described
herein.

Knowledge Skills and Abilities

DATA ENTRY/CRT

TYPING-MEDICAL

EDITING/PROOFING

MEDICAL TERMINOLOGY

CORRESPONDENCE

DATA VERIFICATION

DATA CODING-GENERAL

PC WORDPROCESSING SOFTWARE

PC DATABASE MGT SOFTWARE

Level Characteristics

N/A

Education

Work requires knowledge of basic mathematical, data collection and
research principles normally acquired through an associate's degree.

Experience

Work requires one year experience in research or a clerical setting to
become familiar with the basic techniques and methods used to collect,
compile, verify and store information.

OR AN EQUIVALENT COMBINATION
OF RELEVANT EDUCATION AND/OR EXPERIENCE

Degrees, Licensures, Certifications

N/A
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