
Clinical Study Coordinator
Welcome to Henry Ford Health System, where our mission is to provide compassionate, personalized care to our patients. We are currently seeking a dedicated and detail-oriented Clinical Study Coordinator to join our team. As a Clinical Study Coordinator, you will play a vital role in our research efforts, ensuring the successful execution of clinical trials and studies. We are looking for a motivated individual with a strong background in healthcare and a passion for making a difference in the lives of others. If you are organized, efficient, and have excellent communication skills, we encourage you to apply for this exciting opportunity.
- Coordinate and oversee the execution of clinical trials and studies within the organization.
- Ensure compliance with all regulatory requirements and ethical standards for conducting clinical research.
- Develop and maintain relationships with study sponsors, investigators, and other key stakeholders.
- Facilitate the recruitment and enrollment of eligible participants for clinical trials.
- Collect and maintain accurate and detailed records of study data and participant information.
- Coordinate study procedures and schedules, including participant visits and assessments.
- Assist with the preparation and submission of study protocols, informed consent forms, and other study documents.
- Monitor study progress and ensure adherence to study protocols and timelines.
- Collaborate with the research team to resolve any issues or concerns that arise during the course of the study.
- Communicate study updates and progress to study sponsors, investigators, and other stakeholders.
- Maintain confidentiality and privacy of study participants and their data.
- Participate in training and professional development opportunities to stay up-to-date on current research practices and regulations.
- Contribute to the development and improvement of research processes and procedures.
- Adhere to all organizational policies and procedures related to research activities.
- Embody the mission and values of Henry Ford Health System and maintain a high standard of professionalism and dedication to patient care.
Excellent Communication And Organizational Skills.
Bachelor's Degree In A Relevant Field Such As Healthcare, Biology, Or Public Health.
Minimum Of 2 Years Of Experience In Clinical Research Coordination Or Related Role.
Strong Knowledge Of Fda Regulations And Good Clinical Practice (Gcp) Guidelines.
Ability To Work Independently And Collaboratively In A Fast-Paced, Team-Oriented Environment.
Budget management
Quality Control
Data collection
Project coordination
Regulatory compliance
Time
Clinical Trials
Informed Consent
Protocol Management
Patient Monitoring
Subject Recruitment
Study Documentation
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
flexibility
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Clinical Study Coordinator in Detroit, MI, USA is between $45,000 - $60,000 per year. This can vary depending on factors such as years of experience, education level, and specific job responsibilities.
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The Henry Ford Health System is a comprehensive, integrated, non-profit health care organization in Metro Detroit. The corporate office is at One Ford Place, Detroit, Michigan. Henry Ford established the health system in 1915, and it is currently run by a 15-member board of trustees.

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