In-House Clinical Research Associate I, Sponsor-Dedicated (Contract)
About The Position
Premier Research is looking for an In-House Clinical Research Associate I, Sponsor-Dedicated (Contract) to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. Your ideas influence the way we work, and your voice matters here. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Join us and build your future here.
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
- Demonstrates excellent English verbal and written communication skills
- Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverable, and task ownership
Nice To Haves
- Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred
Responsibilities
- Partners with cross-functional team members and study sites throughout all phases to offer support of numerous trial elements for the clinical operation teams.
- Carry out remote monitoring of clinical trials
- Serves as the secondary contact for sites supporting CRAs
- 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
- Ensures any identified non-compliance issues are addressed, clearly communicated, documented and escalated as required through monitoring visits, analyzing study metrics, and general study data overview
- Assists with audit/inspection readiness, study start-up activities, data listing reviews, monitoring visit support and issue resolution
- Participate in study-specific meetings, teleconferences and training as needed
Benefits
- We provide our staff with innovative technologies and continuous learning.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Entry Level
