Clinical Research Associate

Adecco Medical & Science

Posted: June 29, 2016

Job ID: 162

Job Summary

Term: Full-Time
Job Roles: Clinical Trial Monitoring, Trial/Study Management, Clinical Trial Management System (CTMS), Electronic Data Capture (EDC)
Therapeutic Experience: Oncology
Required Education: Bachelor's
Required Experience: 2 years
Compensation: $80-100,000 DOE

Job Description

A Clinical Research Associate (CRA) job in San Diego, CA needs to be filled immediately by Adecco Medical & Science. This is a direct hire opportunity. In this position you will perform and coordinate all aspects of the clinical monitoring and site management process in accordance with ICH E6 Good Clinical Practices, FDA guidelines, local regulations and standard operating procedures. Additionally, you'll be responsible for performing the clinical monitoring aspect of designated projects in accordance with applicable SOPs; performing clinical on-site monitoring activities. You will also be performing qualification, initiation, monitoring and termination visits of investigational sites, writing visit reports and completing all follow up actions in accordance with ICH GCP guidelines.This position is office based.

Clinical Research Associate job responsibilities:
• Assists in development of study materials, case report forms (CRFs), informed consent documents for clinical studies, as needed.
• Participates in investigator site selection.
• Assists in coordinating activities for the conduct of clinical studies and interactions with CROs and other outside vendors.
• Performs protocol specific as well as GCP training for site personnel
• Continuously evaluates site performance and performs additional site training if needed
• Maintains all relevant site communications and both trial and site master files.
• Communicates regularly with sites and is aware of the activities of assigned clinical sites.
• Conducts and coordinates all activities, including report writing, associated with initiation, interim monitoring, study close out and audit visits as assigned.
• Communicates with internal departments as needed, including attending required meetings and following-up on action items.
• Assists in development of departmental processes, SOPs and personnel training programs.
• Verifies study data and facilitates the resolution of data queries and requests from Data Management.

Requirements:
• BS or RN degree required in a scientific or related field.
• Minimum 1-2 years of CRA experience within oncology is REQUIRED.
• Proven clinical monitoring skills required.
• Demonstrated understanding of medical terminology.
• Ability to attain and maintain a working knowledge of Good Clinical Practices and applicable Standard Operating Procedures.
• Computer skills required-must be proficient in Word, Excel, and PowerPoint.
• Excellent communication skills, ability to communicate effectively with all levels at the clinical sites and good people skills critical.
• Ability to handle multiple tasks to meet deadlines in a dynamic environment.
• Flexibility; ability to travel up to 50-60%+.

If you are interested in this Clinical Research Associate (CRA) job in San Diego, CA then please click APPLY NOW. For other opportunities available at Adecco Medical and Science go to www.adeccousa.com or email your resume to melody.lam@adeccona.com