In-House Clinical Research Associate II
Premier Research
full-time
Posted on:
Location Type: Remote
Location: Massachusetts • North Carolina • United States
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Salary
💰 $49,000 per year
About the role
- Partnering with cross-functional team members and study sites throughout all phases to offer support of numerous trial elements for the clinical operation teams
- Carrying out remote monitoring of clinical trials
- Serving as the secondary contact for sites supporting CRAs
- Maintaining regulatory documents and study supplies throughout the lifecycle of assigned project
- Responsible for the proper reporting and follow up of SAEs and ensures all reportable events are identified, clearly documented and reported per protocol as well as applicable requirements and regulations
Requirements
- Bachelor’s degree, or international equivalent from an accredited institution, preferably in a clinical, biological, scientific, or health-related field or equivalent combination of education, training and experience
- 3 to 5 years of practical experience in clinical trials. Alternately, a proven experience in all primary job functions
- Participate in study-specific meetings, teleconferences and training as needed
- Strong analytical and organizational skills, able to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities
- Prior experience with clinical systems preferred (e.g. eTMF, CTMS, EDC, etc.)
Benefits
- health insurance
- retirement plans
- paid time off
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trialsregulatory document maintenanceSAE reportingevent documentationproject management
Soft Skills
analytical skillsorganizational skillsindependent workmultitaskingadaptability