Clinical Research Coordinators

At Advarra, we seek to foster an inclusive and collaborative environment where everyone is treated with respect and diverse perspectives are embraced. Treating one another, our clients and clinical trial participants with empathy and care are key tenets of our culture at Advarra; we are committed to creating a workplace where each person is not only valued but empowered to thrive and make a meaningful impact.

Our people—both employees and consultants—are the heart of Advarra. They are the key to our success and the driving force behind our mission and vision. Our values (Patient-Centric, Ethical, Quality Focused, Collaborative) guide our actions and decisions. Knowing the impact of our work on trial participants and patients, we act with urgency and purpose to advance clinical research so that people can live happier, healthier lives.

Advarra is seeking Clinical Research Coordinators to join our consultant network for upcoming opportunities. Coordinators support the planning, conduct, and oversight of clinical research projects across a variety of therapeutic areas.

• Coordinate research projects and support study execution.
• Collect, analyze, and manage clinical data.
• Collaborate with cross-functional teams to maintain study compliance.

This is an evergreen role open to candidates in the US. Opportunities may be remote or onsite depending on client needs.

• Bachelor’s degree with three (3) years of relevant experience, OR associate’s degree with four (4) years.
• Experience in clinical research operations and study coordination.
• Strong communication and organizational skills.
• 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

Equal Opportunity Employer
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