- Location
- Regional_NC, United States of America
- Workplace
- Remote
- Type
- Full-time
- Department
- Healthcare
- Seniority
- Entry
- Source
- Workday
Description
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:
Works with Clinical Team Trial Execution team to assist with specific study start up tasks for studies.
Coordinates logistics and planning of meeting, events, and training
Primary lead to disseminate announcements and training materials related to clinical system updates and enhancements, as required
Co-Leads and participates in project team meetings, prepares meeting minutes, and maintains action/decision logs
Create, maintain and provide quality checks for tracking tools and database repositories for operational data including Key Performance Indicators (KPIs) and quality metrics
Performs Clinical Inspection Readiness and Quality Management System activities (e.g., deviations and CAPAs)
What we are searching for:
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
0-2 years of practical experience with clinical trial administration (e.g. – Inhouse CRA, CTA, site administration, project coordination) preferred
Ability to adapt and work on multiple tasks to assist study teams and/or sponsor with various tasks within clinical research highly preferred
Strong ability to communicate effectively with sponsor, study teams and vendors to achieve deadlines for task assigned is ideal
Strong analytical and organization skills, able to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities highly preferred
Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The annualized starting base pay for this role is $44,000 USD. The actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and paid time off.
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
