Patient Enrollment Coordinator – US Clinical Trials (Evening Shift)

About the role

Minerva Research Solutions is seeking a Patient Enrollment Coordinator to manage US‑based clinical trial participants during the evening shift. The role involves screening leads, maintaining participant records, and supporting recruitment efforts for active studies.

Key responsibilities

• Conduct phone interviews and screenings for prospective clinical study participants in the US.
• Maintain an organized database of clinical study participants in the 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 and uphold a safe, positive work environment.

Required profile

• Bachelor’s degree in BDS or Pharm‑D.
• Good knowledge of clinical trials and 6 months to 1 year relevant experience.
• Computer literate with strong proficiency in Microsoft Office.
• Excellent written and spoken English; therapeutic communication with a US accent preferred.
• Strong problem‑solving, teamwork, and planning skills.

What we offer

• Competitive salary with performance‑based incentives and quarterly bonuses.
• Comprehensive medical health insurance for employees, spouses, and children.
• 40‑hour work week promoting work‑life balance and generous annual leave.
• Professional learning, training, and career development opportunities.
• Modern office with fitness gym, recreation zone, and employee‑recognition programs.