Job Description
job Code
#5237
Title
Lead Nurse Coordinator-Clinical Trials
Date Posted
01/29/2018
Job Type
Direct Hire
Job Location
Connecticut
Salary
92,000.00 to 92,000.00
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Lead Nurse Coordinator-Clinical Trials

 

Lead Nurse Coordinator –Clinical Trials

Nurse Staff Manager-Research

 

Design and develop activities, policies and procedures to improve day to day efficiency of studies. 

 

Ensures that the staff performs activities within established protocol, implements procedures and quality assurance standards for the studies.

 

Manage study staff, makes recommendation solutions to improve the overall safety of operations of clinical trials.

Evaluates clinical research trials, studies and projects.

Designs activities, policies and procedures to improve day to day efficiency of the recruitment and assessment components of the study and to ensure that staff members perform activities within established research protocol.

Develops and implements procedures and data quality assurance standards for safety monitoring components of studies.

Writes and edits study protocol.

Develops administrative policies to ensure that staff are performing activities within established protocol, guidelines and federal regulations.

Provides immediate and urgent medical care to subjects experiencing medical complications

Reports critical events and adverse reactions.

Prepares and adjusts recruitment and assessment study plans by designing strategies and analyzing data related to these components.

Trains, develops goals and supervises a team of research staff in the details of the study protocols. Monitors staff schedules, productivity and performance.

Leads committees or task forces to address and resolve significant operational issues.


Requirements:

RN License Registered Nurse in CT or CT license eligible

Education: BSN , Masters in Nursing preferred

Experience: five years of clinical trials and or research experience

Management: 3-5 years in a Lead or staff management related role

Clinical Trial experience with investigator initiated and pharmaceutical research processes.

Working knowledge of federal regulations and guidance documents for the conduct of clinical trials

Strong organizational and interpersonal skills.

Excellent verbal and written skills

Strong Electronic Medical Records technology background; clinical trial databases and patient tracking systems


Send confidential resume to KrishaM@JMorrissey.com

Fulltime Opportunity/excellent benefits/Direct Hire (not contract)

no visa sponsorship available