Hello, my name is Chandrasekhar and I am a Staffing Specialist at Intellectt Inc.
In the past year, we've worked with several medical device clients and helped many candidates to get their careers started.
Hence, I am reaching out to you about an exciting job opportunity with one of our clients.
Please find the below job Description and let me Know your Response
Role: Clinical Research Associate
Location: San Diego, CA
Duration: 7 + Months
Shift Timings: 8 AM to 5 PM
ONSITE POSITION
Job Description:
- 5+ Years Experience Required
- Travel can be up to 30 %-
- Previous Site Monitoring Experience prefers candidates to have Medical devices or Pharmaceutical Background
- This is an onsite role in San Diego.
- Member of the clinical team responsible for conducting Phase I-IV single or multi-center studies according to Federal Regulations and ICH guidelines.
- Responsible for assisting senior staff in planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.
- Responsible for writing basic study protocols, monitoring or overseeing the monitoring of investigational sites to ensure protocol adherence, assuring timely enrollment of patients and retrieval of CRFs from study sites, processing CRFs including data cleanup and classification of data, and completion of study summary.
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