Clinical Research Associate/CRA/Senior CRA
Job Code: CSA0418A
Nationwide
Description
The clinical research associate monitors activities at clinical study
sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study
protocols. Review regulatory documents as required and prepare site visit
reports. Responsible for multiple projects and must work both independently
and in a team environment. May participate in the study development and
start-up process including reviewing protocols, designing and/or reviewing
CRFs, preparing Informed Consent forms, developing study documents,
organizing and presenting at investigator meetings, working with management
on monitoring strategy, and/or developing project-specific CRA training. May
participate in clinical training programs and maintain awareness of
developments in the field of clinical research as needed.
Position will be filled at a CRA or a Sr CRA level depending on experience
and may include customer-managed clients.
Qualifications
- Prefer BS/BA.
- 1 year monitoring experience or combination of on-site monitoring
and clinical research coordinator experience.
- Customer service orientation.
- Sound knowledge of medical terminology and clinical monitoring
process.
- In depth therapeutic and protocol knowledge as provided in company
training.
- Ability to perform regionalized travel an average of 65%, depending
on project needs.
- Excellent verbal and written communications skills.
- In depth therapeutic and protocol knowledge as provided in company
training
- Excellent interpersonal and organizational skills and attention to
detail.
- Computer literacy, proficiency in MS Office.
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