Clinical Trials Monitor/Auditor

Basic education, experience and skills required for consideration:

• Bachelor’s degree in biology, chemistry, biochemistry, physiology, nursing, or other related fields. 
• Two or more years of experience as an industry Clinical Research Associate or clinical trial auditor or monitor.

Preferred education experience and skills:

• Oncology and /or hematology clinical trials
• Experience managing clinical trials.
• Experience as a regulatory affairs administrator.
• Familiar with Investigational New Drug procedures, study protocols, the informed consent process, Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), and applicable regulatory requirements.
• Trained and certified as a Clinical Research Associate by the Association of Clinical Research Professionals (ACRP) or as a Clinical Research Professional by the Society of Clinical Research Associates (SoCRA).

Skills/Abilities:

• Exceptionally detail oriented
• Ability to efficiently review documents while focusing on specific data
• Research information
• Compile data
• Compose reports, ancillary documentation, and training documents
• Instruct/train others
• Compose letters/memorandums
• Troubleshoot problems
• Excellent oral/written communication and organizational skills
• Foster and promote a positive image and professional appearance.

Additional Information:

• To protect the health of patients and staff and to comply with new State of California mandates, City of Hope staff are required to show proof of full vaccination by September 30, 2021.  Compliance is a condition of employment.   

City of Hope is committed to creating a diverse environment and is proud to be an equal opportunity employer.  All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, or status as a qualified individual with disability.   #LI-GD