Clinical Research Associate

New
  • Location
    Durham, North Carolina
  • Job type
    Contract/Temporary
  • Category
    Medical & Science - Pharmaceutical - Clinical

A Clinical Research Associate role is now available through Adecco Medical and Science. In this role, you will travel to investigational sites to verify that the rights and well-being of human subjects are protected, the reported trial data are complete, accurate, and verifiable against source documents, and that the trial is conducted in compliance with the currently approved protocol, Good Clinical Practices, applicable regulations and applicable standard operating procedures (SOPs). This is a home-based position and you can be located anywhere in the Continental US. You must be flexible and willing to travel at least 65% nationwide.

The responsibilities of the Clinical Research Associate include:


DUTIES AND RESPONSIBILITIES

Conduct investigational site visits (evaluation, initiation, periodic and termination) in order to verify proper storage conditions, accountability, and disposition of the investigational products; maintenance of up-to-date and accurate investigator’s study files; and accurate recording and reporting of adverse events.
Write and submit written reports of investigational site findings and updates tracking systems as required.
May be involved in organizing or participating in investigator’s meetings, clinical study report writing, and the development of protocols, informed consent forms, study procedure manuals, monitoring plans, and case report forms.
Maintain a high level of professional expertise through familiarity with regulatory and clinical literature and continuous education.

EDUCATION REQUIREMENTS

Requires a B.A./B.S., R.N., B.S.N. degree or equivalent experience.

REQUIRED QUALIFICATIONS

Minimum of 3-7 years' experience as a CRA with primary site monitoring responsibilities in the pharmaceutical, biotechnology, medical device, or CRO industry, or equivalent experience, as well as experience in oncology and or cardiology.
Requires successful completion of the CRA Training Program.
Knowledge of regulatory requirements and ICH-E6 guidelines required.
Ability to manage competing demands and to respond cooperatively with shifting priorities.
Keeps abreast of industry standards and conditions.
Identifies and solves problems in a timely manner.
Proficiency with various computer applications such as Word, Excel, and Power Point, required: experience with EDC systems preferred.
Valid driver’s license required.

If you are interested in this Clinical Research Associate role, then please click APPLY NOW. For other opportunities available at Adecco Medical & Science please go to www.adeccousa.com.

Equal Opportunity Employer Minorities/Women/Veterans/Disabled



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Reference number US_EN_2_108165_327910