CLINICAL RESEARCH SITE MANAGER

Pivotal Research Centers has successfully completed over 400 research studies in over 20 indications. Pivotal research specializes in multiple therapeutic areas with a focus in neurological, psychiatric, and selected internal medicine indications. Pivotal Research has three (3) 3 clinical research sites as follows:

Peoria, Arizona Site, 13128 N. 94th Drive, Suite 200, Peoria, AZ 85381
Mesa, Arizona Site, 1220 W. Alma School Rd., Suite 206, Mesa, AZ 85210
Salt Lake City Utah Site, 6770 South 900 East, Suite 100, Midvale, UT 84047

COMPENSATION: Negotiable based on experience and qualifications.

JOB DESCRIPTION:

The Mesa, AZ site of Pivotal research is currently seeking a Clinical Site Manager. If you have a minimum of 3 years of research coordinating experience, some management experience, and have a bachelor’s degree (phlebotomy a plus), join one of the top medical research centers in the Southwest. Pivotal is looking for an energetic, well-organized, person with a positive and friendly attitude, who also possesses proven clinical research, management and interpersonal skills. Varied office hours, a competitive salary, growth opportunities, benefits, and a friendly work environment await you! Fax HR at: 623-583-0299 or [Click here for email].

POSITION: Clinical Site Manager (in Mesa)

REQUIREMENTS: R.N. (preferred)
3 years clinical research coordinating experience (minimum requirement)
1 year management experience

CATEGORY: Full-Time Employment - Salary
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General Responsibilities:

·Report to Chief Executive Officer (CEO)
·Responsible for supervision / management of site
·Responsible for enrollment and overall success of site’s clinical trials
·Responsible for day-to-day operations
·Participate in interviewing and hiring process for site
·Participate in performance evaluation process for site employees
·Maintain an understanding of all ongoing and enrolling clinical trials
·Supervise enrollment of clinical trials to ensure that all recruitment goals and deadlines are met
·Actively participate in the conduction of weekly staff meetings
·Provide weekly update of clinical trials’ status to administration
·Ensure adherence of clinical staff to Guidelines of Practice and GCPs
·Initiate and/or participate in disciplinary actions of clinical staff
·Ensure clinic compliance with FDA, IRB, OSHA, FMLA, ADA, and other applicable regulatory agencies
·Maintain understanding of regulatory process and status with our regulatory department
·Maintain high level of inter-rater reliability within clinic psychometric testing
·Act as resource person and assist with problem solving for clinical staff
·Monitor and evaluate the ongoing recruitment of each clinical trial
·Interview/Screen patients & perform informed consent as required according to Pivotal Guidelines of Practice as required
·Willingly work flexible hours to accommodate clinical trials and clinic schedule in a reasonable manner
·Communicate directly with sponsors and appropriate representatives as required
·Treat patients and colleagues with respect and dignity
·Work as a team player at all times
·Demonstrate mature judgment, professional conduct, and exhibit absolute frankness at all times
·Perform other duties as required

Clinical Trial Management Responsibilities:

·Supervise clinical staff during conduction of clinical studies to ensure adherence to clinical protocols
·Actively supervise and participate in clinical trial startup
·Meet with CRA / Monitor during site visits to discuss clinical trial issues
·Actively supervise and participate in post monitor visit meetings
·Maintain clinical coordinator skills to be available as backup as needed
·Act as preceptor and / or mentor as required in the training and development of the clinical research coordinator staff

CONTACT INFORMATION:

All interested candidates send your resume via fax or e-mail as directed below.

Contact information email:
[Click here for email]
Fax: 623-583-0299

THANK YOU VERY MUCH FOR YOUR INTEREST IN PIVOTAL RESEARCH CENTERS - creating hope through medical research.
REQUIREMENTS
See above for all job requirements. Thank you.