In-House Clinical Research Associate I, Sponsor-Dedicated (Contract)
Premier Research
Summary
Premier Research is looking for an In-House Clinical Research Associate I, Sponsor-Dedicated (Contract) to join our Functional Services Provider (FSP) team.
Job description
What you'll be doing:
- 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
What we are searching for:
- Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred
- 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
- 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
- Preferred Location: East Coast / Central
This is a 1099 12-month contract position with the potential to extend and renew after 1 year.
Requirements
- Experience in Neurology or Psychiatry, including work with Schedule I controlled substances, is highly preferred
- 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
- 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
- Preferred Location: East Coast / Central
Company overview
Premier Research International LLC is a global leader in clinical research and consulting services dedicated to helping biotech, specialty pharmaceutical, and medical device innovators transform breakthrough science into life-changing therapies. Founded in 1989, the company specializes in addressing trial complexity, overcoming development hurdles, and demonstrating product value through integrated end-to-end solutions. With deep therapeutic expertise across oncology, hematology, immunology, rare diseases, cell and gene therapy, and women's health, Premier Research leverages innovative technology and operational proficiency to deliver accelerated development timelines. The company operates globally with over 2,000 employees across more than 70 countries, managing clinical trials from preclinical planning through commercialization. Premier Research's mission focuses on turning brilliant ideas into new medical treatments by providing personalized clinical research, product development, and consulting services that help answer unmet patient needs across a broad range of medical conditions.