Clinical Research Coordinator

Insight Global; Farmington Hills (MI); On-site; USD 42,000 - 64,000; Full time

Job summary

Insight Global is seeking a Clinical Research Operations Coordinator to support participant recruitment, scheduling, and study operations for a clinical research initiative. This onsite role at a clinic serves as the primary liaison between the research team and clinical site staff to ensure a smooth participant experience and successful study execution.

The role emphasizes recruitment and scheduling, with exposure to enrollment and moderated sessions to understand the study process, while

Qualifications

• 2+ years of clinical research coordination or related experience.
• Experience working directly with patients or research participants.
• Bachelor's degree in life sciences, healthcare, public health, psychology, or related field.

Responsibilities

• Coordinate participant recruitment, screening, and enrollment activities.
• Schedule participant visits, study sessions, and follow-up appointments.
• Serve as the primary point of contact between the research team and clinical site staff.
• Track recruitment progress and help maintain study timelines.
• Communicate with participants and stakeholders to ensure smooth study operations.
• Support participant enrollment and moderation sessions as needed to develop an understanding of the participant experience and study workflow.
• Maintain accurate study records and documentation.

Skills

Organizational skills

Communication skills

Coordination skills

Clinical research coordination

Education

Bachelor's degree in life sciences or related field

Job description

We are seeking a Clinical Research Operations Coordinator to support participant recruitment, scheduling, and study operations for a clinical research initiate. Based primarily onsite at a clinic, this individual will serve as a key liaison between the research team and clinical site staff, ensuring a seamless participant experience and successful study execution. The role will focus primarily on participant recruitment, scheduling coordination, and operational support, while also gaining exposure to participant enrollment and moderated research sessions to build a comprehensive understanding of the study process.

Responsibilities

• Coordinate participant recruitment, screening, and enrollment activities.
• Schedule participant visits, study sessions, and follow-up appointments.
• Serve as the primary point of contact between the research team and clinical site staff.
• Track recruitment progress and help maintain study timelines.
• Communicate with participants and stakeholders to ensure smooth study operations.
• Support participant enrollment and moderation sessions as needed to develop a strong understanding of the participant experience and study workflow.
• Maintain accurate study records and documentation.

Qualifications

• 2+ years of experience in clinical research coordination, participant recruitment, patient scheduling, or clinical trial operations.
• Experience working directly with patients or research participants.
• Strong organizational, communication, and coordination skills.
• Familiarity with clinical research processes and participant-facing activities.
• Bachelor's degree in a life science, healthcare, public health, psychology, or related field required

Shift: Mon - Friday 8-6 *hours may vary, Study will run until End of Year