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:
Supplemental pay types:
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