Clinical Trials Clinical Coordinator Jobs
METROPLEX CLINICAL RESEARCHCENTER CLINICAL TRIAL ASSISTANT REPORTS TO:Site Director FUNCTION:Provide Administrative and Regulatory Support OVERVIEW OF DUTIES AND RESPONSIBILITIES Assist in set up and maintenance of study files Create templates for documents Create source documents required for study conduction QA/QC with in-house tracking processes of all source documents Track and maintain staff...
The Stanford University NCI Designated Cancer Center seeks a Cancer Clinical Trials Financial Specialist. This position will report to the Cancer Clinical Trials Office (CCTO) Financial Manager. The Cancer Clinical Trials Financial Specialist is the Institutional Representative for sponsored cancer clinical trials and is the primary point of contact for sponsor and University clinical research gra...
In this start up role, the Manager, Clinical Trials (Office of Commercialization & Ventures) will work closely with internal staff members and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a manner compliant with all regulatory guidelines, organizational goals and established study budgets. In this exciting venture, The Manager, Clinical Tri...
Job ID: 24630 Date Posted: 07/08/2014 Location: 450 Brookline Ave Job Family: Clinical Research Coordinator Full/Part Time: Full-Time Regular/Temporary: Regular FLSA Status: Nonexempt Overview Located in Boston, Dana Farber Cancer Institute brings together world renowned clinicians, innovative researchers and dedicated professionals, allies in the common mission of conquering cancer, HIV/AIDS and...
The Cancer Clinical Trials Office (CCTO) is an integral component of Stanford’s National Cancer Institute (NCI) Designated Cancer Institute since it enables the objective of our cancer center, to translate research from the laboratory into the clinical setting. There are more than 300 clinical trials open to accrual at any time within the Cancer Institute. More than one-third of these trials are I...
NSABP NSABP Foundation, Inc The NSABP, is seeking an experienced individual to perform activities related to the administration of clinical trials. Send resume to *****. or fax to NSABP HR at 412-339-5308. Clinical Trial Senior Project Coordinator and Compliance Specialist Responsibilities Include: - User liaison to Info. Technology Dept. for ongoing improvements and maintenance...
Company Confidential Peace Haven Estates, NC, 27104
Full-Time Clinical Research Nurse Coordinator Become part of a company who participates in research with results. PMG strives to bring clinical research to as many lives as possible while delivering unparalleled service and exceptional value to our clinical trial partners and stakeholders. Job Description: PMG Research of Winston-Salem is seeking an enthusiastic medical professional for an excitin...
JOB DESCRIPTION DEPARTMENT: Needham Clinic REPORTS TO: Principal Investigator / Optometrist EXEMPT OR NON-EXEMPT: Exempt POSITION SUMMARY: The Boston Foundation for Sight (BFS) restores the sight and reclaims the lives of patients with complex corneal disease. Under the direction and supervision of the BFS medical staff, this position facilitates all implementation phases of new studies as well as...
Clinical Value Analysis Coordinator St. Joseph Health System Bryan, Texas St. Joseph Health System is currently seeking a Clinical Value Analysis Coordinator who will help introduce, evaluate and standardize new products and technology. As Clinical Value Analysis Coordinator, you will review and present identified savings opportunities to our Value Analysis Teams. You will coordinate product trial...
Analyzes, reviews, develops, initiates, and negotiates contractual arrangements for clinical research protocols with industry sponsors/collaborating sites. Assists in managing contract development and negotiation from inception through revisions to finalization, ensuring mitigation of risk of loss and liability. Reviews and understands research protocols and ensures compliance with federal, state,...
EXPERIENCED Clinical Research Coordinator needed full time to join our growing practice performing clinical research trials at our Memorial City branch. Competitive salary and benefits....
Clinical Research Study Coordinator. FT to participate in conducting clinical trials for private practice in Troy. Responsibilities include subject recruitment, enrolling patients into various studies, following patients through the study. Previous research exp pref’d but not req’d. Bachelor degree req’d. Send resume to: *****....
Description The Clinical Research Coordinator is responsible for coordinating and organizing clinical studies and/or trials. Under general supervision, follows the participant or patient from recruitment through treatment, discharge and follow-up. Provides patient and family education and maintains records and documentation. Maintains a working nursing knowledge of cardiology. May perform general...
Company Confidential KNOXVILLE, TN, 37917
Clinical Research Coordinator: Need CCRC, LPN, or RN to work with MD on Cardiovascular Clinical Trials. Ideal candidate is energetic, compulsive, organized, hard-working self-starter with patient care skills and clinical trial experience. Job involves patient recruitment, phlebotomy, protocol compliance, data management, work with regulatory agencies (FDA, IRB), familiarity with GCP. Submit resume...
The Clinical Trials Coordinator will be responsible for providing support to the Clinical Study Manager. Duties include but are not limited to set up and maintain tracking system for patient visits, contracts, budgets, invoices, vendor and site payments, regulatory documents, IRB approvals, etc. Assist Study Manager with electronic study tracking and maintaining a shared electronic study database....
Scope of the Job Under the general direction of the Research Administrator, the Research Specialist is responsible for assuring that the integrity and quality of the research activities are maintained and conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and UF IRB Policy and Procedures. The Research Specialist is assigned research trials for coordinat...
Clinical Research Coordinator Become part of a company who participates in research with results. PMG strives to bring clinical research to as many lives as possible while delivering unparalleled service and exceptional value to our clinical trial partners and stakeholders. We are seeking a full time Clinical Research Coordinator for our Clinical Research Site based in Knoxville, TN. The Clinical...
Excellent opportunity to join a department conducting pharmaceutical research trials. Seeking a highly motivated, organized and detailed individual who works well independently. Full time position with good benefits offered. EOE Experienced Clinical Research Coordinator RN/LPN Preferred www.heartlandresearch.com...
Drexel is a comprehensive global research university ranked among the top 100 in the nation. With approximately 25,000 students, 200 degree programs and 14 colleges and schools, Drexel is one of America’s 15 largest private universities. One of Philadelphia’s top 10 employers, Drexel is a major engine for economic development in the region. The Philadelphia Business Journal ranks Drexel as one of...
Title: Clinical Affairs Coordinator Essential Functions: Maintain Master Document Tracker File hard copies and maintain an electronic master document tracker that includes but is not limited to the following information: site contact information, Investigator Background form, non-disclosure agreement, W-9, financial disclosure forms, signed clinical trial agreements/budget, protocol signature page...
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Administrative Career Tools
Clinical Coordinator-Clinical Trials
$31,200.00 - $83,200.00
Typical Salary for Clinical Coordinator-Clinical Trials
Source: Monster.com Careerbenchmarking Tool
Education / Training
Some College Coursework Completed
Source: Monster.com Careerbenchmarking Tool
Clinical Coordinator-Clinical Trials
Plans and controls clinical pharmacology studies by developing and implementing research and administrative strategies, exclusive of those actions requiring medical judgments; standardizing operating procedures across all trials; supervising staff.
Rate of Growth
Size of Industry in 2006:
Source: Bureau of Labor Statistics, May 2006
Administrative Writing Skills
Health Promotion and Maintenance
Maintains patient confidence and protects operations by keeping information confidential.
Ensures clinical trials site compliance with protocol specifications, FDA, and other regulatory obligations by visiting investigative sites; conferring with site coordinators and physicians; implementing protocols; monitoring trials at sites; making recommendations as warranted to assure adherence to Federal Drug Administration and protocol guidelines; identifying potential problems and/or inconsistencies; taking action as appropriate.
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