Clinical Research Coordinator

Responsibilities

• The Clinical Research Coordinator coordinates pharmaceutical company, National Cancer Institute (NCI), multisite and in-house protocol activities for the Cancer Program and principal investigators
• Adheres to federal regulations, sponsor guidelines, medical center policies and procedures; and performs related work as required
• Supports the Mission of Trinity Health and Holy Cross Hospital

Preferred

• Master's Degree in a health-related field (preferred.)
• Good Clinical Practice (GCP) Certification (preferred)
• Clinical research certification (preferred)

Benefits

• Medical, dental, vision, and mental health benefits available from the first day of employment for Full & Part-Time colleagues.
• Paid time off available from the first day of employment for Full & Part-Time colleagues.
• 403B available from the first day of employment for Full & Part-Time colleagues.
• Education assistance available from the first day of employment for Full & Part-Time colleagues.
• Voluntary benefits (pet insurance, accident insurance, hospital indemnity and others) available from the first day of employment for Full & Part-Time colleagues.
• Free parking.
• A culture that nurtures a healing, safe environment for all.
• Referral Rewards Program.
• Glassdoor
• 3.4
• Trinity Health is one of the largest multi-institutional Catholic health care delivery systems in the nation.
• Livonia, Michigan, USA
• http://www.trinity-health.org
• Late Stage
• Total Funding
• $0.02M
• Key Investors
• Centers for Disease Control and Prevention
• 2025-10-17
• Grant· $0.02M
• Leadership Team
• Dan Drake
• Trinity Health PACE President and CEO
• Eileen Coogan
• Pres/CEO Allegany Franciscan Ministries
• Recent News
• Fierce Healthcare
• Readily secures $11M series A to continue building out AI regulatory compliance platform
• 2026-10-17
• Allara raises $30M to expand virtual women's healthcare across the continuum

Qualifications

• Bachelor's Degree required
• Active Driver's License required
• Basic Life Support (BLS) Certification
• Must have knowledge of cancer and clinical protocols
• Three years or more experience in research program leadership
• Sufficient healthcare experience: 3-5 years related clinical research and project management experience
• Ability to communicate effectively, both orally and in writing
• Ability to create and conduct presentations to public and professional audiences
• Ability to analyze and synthesize data, prepare and present reports as necessary
• Ability to maintain patient confidentiality
• Ability to understand federal regulations and translate those regulations to guide the research work
• Ability to facilitate and lead a multidisciplinary team of professionals involved in research studies
• Master's Degree in a health-related field (preferred.)
• Good Clinical Practice (GCP) Certification (preferred)
• Clinical research certification (preferred)
• Three years or more experience in research program leadership.
• Sufficient healthcare experience: 3-5 years related clinical research and project management experience.

Required skills

• Basic Life Support (BLS), Cancer, Clinical Practice (GCP), Clinical Protocols, Clinical Research, Clinical Research Certification, Data Analysis, Federal Regulations, Research Program Leadership

Preferred skills

• Clinical research certification (preferred), Good Clinical Practice (GCP) Certification (preferred), Master's Degree in a health-related field (preferred.)

Experience

• 3-5 years