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Benefits offered by this job
Annual Bonus
RSUs
Job summary
A clinical research firm is seeking a Site Director for Clinical Operations in the Midwest Region. This role involves managing clinical site activities, ensuring compliance with regulations, and leading Phase I-IV studies. Candidates should have at least 3 years of site monitoring experience and a Bachelor’s degree in Life Science. Strong interpersonal and critical thinking skills are essential. This is a full-time position with a salary range of $160,000 to $200,000, remote options available from Chicago, Minneapolis, or Wisconsin.
Qualifications
Minimum 3 years of direct site monitoring experience.
In-depth knowledge of clinical site monitoring and drug development.
Strong understanding of FDA, ICH, GCP guidelines.
Responsibilities
Lead start-up and monitoring of Phase I-IV studies.
Primary contact for sites throughout study phases.
Ensure data accuracy through source data verification.
Skills
Clinical site monitoring
Critical thinking
Interpersonal skills
Detail-oriented
Team collaboration
Education
Bachelor’s degree in Life Science
RN preferred
Tools
CTMS
eTMF systems
Job description
A clinical research firm is seeking a Site Director for Clinical Operations in the Midwest Region. This role involves managing clinical site activities, ensuring compliance with regulations, and leading Phase I-IV studies. Candidates should have at least 3 years of site monitoring experience and a Bachelor’s degree in Life Science. Strong interpersonal and critical thinking skills are essential. This is a full-time position with a salary range of $160,000 to $200,000, remote options available from Chicago, Minneapolis, or Wisconsin.