Clinical Research Associate - Vermont, United States - Advarra

Description

About Advarra:

Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial participants, empower clinical sites, ensure compliance, and optimize research performance for over 3,500 sponsors, CROs, institutions, academic medical centers, and research consortia.

With trusted and unequaled independent oversight committee services, innovative software solutions for sites, sponsors, and CROs, and experienced consultants with deep-seated connections across the industry, Advarra has the expertise and technology needed to advance clinical research and help our clients make the world a healthier place.

About the Opportunity:

Do you have an interest in joining talented and passionate clinical research professionals? Advarra is seeking Clinical Research Coordinators II/III to join our talent pool for future opportunities.

The Clinical Research Coordinators II/III roles are consulting (contractor) roles. These are not permanent positions with benefits.

Join our talent pool and be empowered to thrive and make a meaningful impact

Clinical Research Coordinator II

The Clinical Research Coordinator II will plan, direct, and coordinate clinical research projects along with evaluating and analyzing clinical data.

Credentials and Qualifications:

• Bachelor's degree with three (3) years of relevant clinical, health related, scientific, business or research experience or Associate's degree with four (4) years of relevant clinical, health related, scientific, business or research experience.
• Certified Clinical Research Professional (CCRP)/Certified Clinical Research Coordinator (CCRC)/Society of Clinical Research Associates (SOCRA) certifications or equivalent preferred
• Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy

Clinical Research Coordinator III

The Clinical Research Coordinator III will plan, direct, and coordinate clinical research projects along with evaluating and analyzing clinical data. This role requires mentorship and leadership skills along with the ability to work independently.

Credentials and Qualifications:

• Bachelor's degree with six (6) years clinical trials coordination experience. In lieu of a bachelor's degree, an Associate's degree with 8 years of clinical trials coordination experience may be considered
• Certified Clinical Research Professional (CCRP)/Certified Clinical Research Coordinator (CCRC)/Society of Clinical Research Associates (SOCRA) certifications or equivalent preferred
• Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy

The benefits of joining the Advarra talent pool include:

• Potentially higher hourly pay rate than working direct
• Part-time and full-time opportunities
• Flexible work schedules
• Work/life balance
• Remote, onsite, and hybrid opportunities available
• Contribute to our values (Patient-Centric, Ethical, Quality Focused, Collaborative) that guide our actions and decisions