CenterWatch

Keep the discussion going--join our JobWatch Group on LinkedIn!

Sign In
 [New User? Sign Up]
Mobile Version

Asst Clinical Research Coordinator

UC Davis Health System


Location:
Sacramento, California
Date:
01/03/2018
2018-01-032018-02-02
Job Type:
Employee
Categories:
  • Clinical Operations
UC Davis Health System
  •  
  • Save Ad
  • Email Friend
  • Print
  • Research Salary

Job Details

Department Description

In the Department of Internal Medicine, Division of Infectious Diseases, industry-sponsored and investigator-initiated or other academic studies are conducted in the field of infectious diseases.

We offer exceptional employee benefits including medical, dental, and vision plans, generous paid vacations and holidays, excellent retirement savings and investment plans, continuing education, and reduced fee and scholarship programs.

Qualifications

REQUIRED

--Excellent skills to exercise discretion, initiative and resourcefulness and make independent judgments

--Experience in independently organizing tasks and set priorities for work assignments to achieve timely progress on multiple tasks simultaneously, to meet deadlines and maintain a high level of productivity

--Experience using advanced-level organizational skills and attention to detail in maintaining large volumes of records

--Excellent oral and written communication skills

--Knowledge of anatomy, physiology, medical terminology and procedures to effectively interpret and accurately compile data according to study protocol

--Excellent mathematical skills

--Proficient computer skills with experience using word-processing programs, database programs, and data management

--Excellent writing and printing skills

 

PREFERRED

--Prior experience as a  Research Coordinator independently comprehending and implementing complex clinical research protocols

--Thorough knowledge and understanding of 'Good Clinical Practices' for clinical research

--Knowledge and understanding of federal, state and university (or similar) regulations for clinical research under Investigational New Drug and Institutional Review Board (IRB) guidelines (or similar)

--Experience coordinating a broad range of activities from inception to implementation within the confines of strict study protocols, University (or similar)  and policies and procedures

 

SPECIAL REQUIREMENT

- THIS POSITION MAY BE SUBJECT TO A CRIMINAL BACKGROUND INVESTIGATION, DRUG SCREEN, LIVE SCAN FINGERPRINTING, MEDICAL EVALUATION CLEARANCE, AND FUNCTIONAL CAPACITY ASSESSMENT

               

Responsibilities

               

The Assistant Clinical Research Coordinator (Assistant CRC) assists with administrative support of research trials and related studies in the Department of Internal Medicine, Division of Infectious Diseases.  The Assistant CRC also helps with several aspects of the conduct of clinical trials, including subject recruitment, screening, enrollment, scheduling, data collection, participant tracking, preparation for audits and monitor visits, study closeouts, and assisting with administrative requirements.  Additional responsibilities include IRB submissions, modifications, and amendments, annual renewals, obtaining financial disclosure information from the investigators, and collection and maintenance of study regulatory documents.  This position is grant funded.

Powered ByLogo