In-House Clinical Research Associate II, Sponsor-Dedicated (Contract)
- Hiring from
- United States
- Work type
- Remote
- Posted
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You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
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.
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.
Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status
Why Choose Premier?
Premier Research is more than a company – it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems.
Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies.
As a Premier team member, you have the power to make an impact, regardless of job title and location.
Our dedication to biotech and specialty pharma is unlike any other.
We provide our staff with innovative technologies and continuous learning.
About Us
Premier Research is a global clinical research, product development, and consulting company. We are dedicated to helping biotech, specialty pharma, and MedTech innovators transform life-changing ideas and breakthrough science into new medical treatments. Our team is inspired by this common purpose. Premier is a place where you can change lives, and feel rewarded and celebrated. We aim high - we will not stop until we reach our goals. And we care about each other, about our customer and partners, and, most importantly, about all the patients that we touch with our work.