Resumes2Work.com - Job Search Engine - Job Alerts - Job Blogs
 
Resumes2Work Home Page Post Your Resume Free! Post your Job Openings here! Other Job Resources Job Search Page
Job Search Engine - Job Alerts - Job Blogs - Resumes2Work.com Job Search Engine - Job Blogs Saturday, November 21, 2009
Advance your career - job search engines - employee recruiting
jobs - career tools - healthcare jobs and more
Resumes2Work
 

Custom Job Blogs Press Release        New Two-Fer Job Posting - Press Release
[ Home | Search Jobs | Create Applicant Account | Create Employer/Agent Account | Log-in | About Us | Contact Us ]
Have you posted your resume/CV on Resumes2Work.com? It might help.

Clinical Research Coordinator II

From:
Company: Medical College of Wisconsin (see all of this employer's jobs)
Phone: 4144564149
Fax: 1234567890
Click Here to Apply

Apply by eMail:do_not_reply@invalidemail.com


Job Reference ID:  5105180

Category:
Education

Duration:  Fulltime, Permanent
City, ST:  Milwaukee, Wisconsin
Country:  United States

Description:
POSITION PURPOSE
 
Perform the day-to-day administrative activities of clinical research trial programs. Provide support to the team to facilitate the achievement of the program’s goals. Assist with recruiting, training, and supervising staff and managing the program budget.
 
 
ESSENTIAL DUTIES
1.    Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants.
2.    Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.
3.    Collect, analyze, and disseminate research data. Report program data and progress to study investigators.  Work with Principle Investigator to develop, implement, and maintain comprehensive databases and files related to the program.
4.    Identify problems or obstacles in the system/procedures related to implementation of the research protocols and communicate to the study investigators.
5.    Assure compliance with all relevant IRB and other regulatory agency requirements.
6.    Prepare IRB documents and reports. Evaluate and write of research protocols in collaboration with the study investigator.
7.    Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports.
8.    Maintain program timeline including tracking deadlines for program components.
9.    Coordinate program outreach activities including acting as a liaison with community organizations.  Organize internal and external meetings, site visits, and special events.
10.Monitor study related budgets.  Participate in the development of program resources through literature searches, contact with outside programs, and review of funding opportunities.
11.Assist in recruitment and training of program staff.  Assist in scheduling people and material resources.
12.Process and ship lab specimens as necessary.
 
 
OTHER DUTIES
 
Perform other duties as assigned.
 
 


Click Here to Apply

Apply by eMail:do_not_reply@invalidemail.com

Job Created: Tue Oct 20 2009 06:40:02 AM
Last Modified: Sat Nov 21 2009 06:51:08 AM


Resume Writing
Get our professional resume writers to write your
Clinical Research Coordinator II resume
and you're 100% guaranteed to get
more interviews and job offers.




copyright © 2003 - 2009 resumes2work | Privacy Policy