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Job summary
A pioneering biotechnology company in Woburn is seeking an experienced Clinical Operations Manager to oversee clinical trials in nephropathies. The ideal applicant will have over 10 years of experience, strong project management skills, and a detail-oriented approach. Responsibilities include managing trial protocols, site selection, and regulatory compliance. Join us to revolutionize therapies with RNAi technology. Interested candidates can send applications to hr@sanegenebio.com.
Qualifications
10+ years of experience in clinical operations, preferably in nephropathies.
Proven track record in trial management and regulatory compliance.
Responsibilities
Lead the planning, execution, and monitoring of clinical trials focused on nephropathies.
Develop and implement clinical trial protocols and informed consent forms.
Coordinate with cross-functional teams for efficient trial execution.
Identify and manage clinical trial sites.
Conduct site visits to monitor trial progress.
Oversee data collection processes and prepare trial updates.
Ensure compliance with FDA, EMA, and ICH guidelines.
Assist in developing and managing clinical trial budgets.
Skills
Project management
Organizational skills
Problem-solving
Communication skills
Collaboration
Detail-oriented
Education
Bachelor’s degree in life sciences, nursing, or related field
Master's degree (preferred)
Tools
Clinical trial management software
Data analysis tools
Job description
A pioneering biotechnology company in Woburn is seeking an experienced Clinical Operations Manager to oversee clinical trials in nephropathies. The ideal applicant will have over 10 years of experience, strong project management skills, and a detail-oriented approach. Responsibilities include managing trial protocols, site selection, and regulatory compliance. Join us to revolutionize therapies with RNAi technology. Interested candidates can send applications to hr@sanegenebio.com.