Clinical Trials Quality Assurance Associate (Night)

About the role

Minerva Research Solutions is seeking a dynamic individual to join its clinical trial team as a Night Clinical Trials Quality Assurance Associate. The role focuses on patient enrollment, screening, and documentation to support active clinical studies, ensuring compliance with FDA and GCP regulations.

Key responsibilities

• Conduct phone interviews and screenings for prospective study participants in the US.
• Maintain an organized database of clinical study participants in the Clinical Trial Management System (CTMS).
• Develop outreach strategies to enhance participant recruitment.
• Interact directly with study participants via phone calls, SMS, and other communication channels.
• Collaborate with medical staff (CRCs) to ensure adequate subject recruitment for each study.
• Enhance and maintain study documentation and volunteer records, including consent forms.
• Assist in sales, marketing, and outreach efforts as needed.
• Provide accurate study‑related information to participants.
• Foster a safe, positive, and fast‑paced work environment.
• Undertake other related duties and participate in special projects as assigned.

Required profile

• Bachelor’s degree in BDS or Pharm‑D.
• 6 months to 1 year of relevant experience.
• Strong English communication skills, both written and spoken; US accent preferred.
• Professional demeanor with strong teamwork and work‑ethic commitment.
• Proactive attitude toward knowledge sharing and continuous improvement.

Required skills

• Proficiency with Microsoft Office applications.

What we offer

• Competitive salary with performance‑based bonuses.
• Quarterly bonus structure.
• Medical health insurance coverage for employee and family (spouse & children).
• Old‑age benefits coverage.
• 40‑hour work week with exposure to the US market.