Job Description

About M1 Health

We are a innovative, customer-centric, and growth oriented organization. Our goal is to "Unlock the Power of Excellence in Clinical Research."

Our work environment includes the following:

• Modern office setting
• Work-from-home days
• Growth opportunities
• Flexible Schedules

Learn more at https://m1-health.com/

Our Culture

Our culture can best be summarized in the following points:

• We believe in giving people autonomy to express their creativity and harness their drive in light of our mission.
• Growth is essential, and as the organization grows, so should the people that support it.
• We believe in fostering a culture of transparency, trust, and meritocracy.
• We believe in being anti-bureaucratic and maintaining efficiency and speed.

Summary: We are seeking an experienced and dedicated Senior Clinical Research Coordinator to join our team and oversee the coordination, management, and execution of clinical research studies. The ideal candidate will have a strong background in clinical research and excellent organizational and communication skills to ensure the successful completion of study objectives while adhering to regulatory and ethical guidelines.

Key Responsibilities:

• Coordinate and manage clinical research studies, ensuring compliance with study protocols, regulatory requirements, and ethical guidelines.
• Supervise and mentor a team of clinical research coordinators, providing guidance and support to ensure high-quality performance and professional development.
• Develop and maintain study-specific documentation, including informed consent forms, case report forms, and study manuals.
• Monitor study progress, ensuring timely recruitment, data collection, and data entry while identifying and resolving any issues that may arise.
• Collaborate with principal investigators, study sponsors, and other stakeholders to develop and implement study protocols, budgets, and timelines.
• Assist in the preparation of regulatory submissions, ethics applications, and study reports.
• Maintain regular communication with study participants, ensuring their safety and well-being throughout the study.
• Ensure proper storage, management, and handling of study-related materials and data.
• Participate in audits, inspections, and quality assurance activities as required.
• Stay current on industry trends, best practices, and regulatory updates to ensure the continuous improvement of clinical research processes.

Qualifications:

• Bachelor's degree in a related field (e.g., life sciences, nursing, or public health); advanced degree preferred.
• Minimum of 5 years of experience in clinical research, with at least 2 years in a leadership or supervisory role.
• Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) designation preferred.
• Strong knowledge of Good Clinical Practice (GCP) guidelines, FDA regulations, and other relevant guidelines.
• Excellent organizational, communication, and interpersonal skills.
• Demonstrated ability to work independently, manage multiple projects, and prioritize tasks effectively.
• Proficiency in Microsoft Office Suite and electronic data capture systems.

Job Type: Full-time

Pay: $79,378.00 - $105,523.00 per year

Benefits:

• Flexible schedule
• Health insurance
• Paid time off
• Professional development assistance
• Relocation assistance

Schedule:

• Monday to Friday

Supplemental pay types:

• Bonus pay
• Signing bonus

Ability to commute/relocate:

• Chicago, IL: Reliably commute or willing to relocate with an employer-provided relocation package (Required)

Experience:

• Clinical Research: 3 years (Required)

Work Location: In person

Similar Jobs