- Hologic (San Diego, CA)
- … teams to plan and execute trials in compliance with Good Clinical Practices (GCP), departmental procedures, and regulatory requirements. + **Communicate ... schedules, and establish key performance indicators (KPIs) to measure success. + ** Regulatory Knowledge:** Strong working knowledge of Good Clinical Practices… more
- Dana-Farber Cancer Institute (Boston, MA)
- …with regulatory authorities. Reporting to disease group managers and/or Clinical Trials Office (CTO) leadership the Clinical Research Project Manager ... and management. **KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED:** + Basic understanding of clinical trial processes and regulatory requirements, including Good … more
- Minnesota State (St. Cloud, MN)
- …Bachelor's Degree + Minimum of ten years of applicable industry experience in Regulatory Affairs, Clinical Research, Quality or Reimbursement + Advanced degree ... Closing Date (if designated).** **Working Title:** Adjunct Instructors - Regulatory Affairs and Services **Institution:** St. Cloud State University **Classification… more
- Rush University Medical Center (Chicago, IL)
- …as assigned. **Preferred Job Qualifications:** **Experience:** * 2-5 years' experience in clinical research conduct and regulatory management, or hold a valid ... may vary depending on the circumstances of each case. **Job Summary:** The Clinical Research Coordinator III (CRC III) independently manages the full scope of … more
- Edwards Lifesciences (Chicago, IL)
- …**As the Manager of Clinical Project Management** , you will manage clinical trials activities and ensure all applicable regulatory requirements are met. ... of Edwards policies, procedures, and international and domestic medical device regulatory guidelines relevant to clinical protocols + Understanding of… more
- Sanofi Group (Cambridge, MA)
- …with the global project team and internal partners, such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, ... SOPs, GCP, ICH guidelines and other regulations + Review documents supporting clinical development such as Investigator's brochure, regulatory documents for IND… more
- HCA Healthcare (Asheville, NC)
- …on assigned campuses. This role ensures high-quality, evidence-based, and regulatory -compliant clinical and simulation-based learning experiences that supports ... with standardized curricula, professional nursing standards, accreditation requirements, and regulatory guidelines. 4. Implements, and oversees clinical … more
- University of Utah (Salt Lake City, UT)
- …In collaboration with investigators, clinical research study teams, and clinical teams, the QA Specialist ensures regulatory compliance, operational ... Quality Oversight** + Conduct routine internal audits and targeted reviews of clinical trial documentation including regulatory binders, subject binders and… more
- Dana-Farber Cancer Institute (Boston, MA)
- …for assisting with the design, implementation and evaluation of their program's clinical research activities, related regulatory oversight, and will provide day ... Research Manager with the oversight of their disease group's clinical trial portfolio and all related regulatory ...group's clinical trial portfolio and all related regulatory and compliance requirements. + Assist the CRM will… more
- ThermoFisher Scientific (Richmond, VA)
- … Clinical Development Plan. + Provide support for critical day-to-day clinical study activities, including regulatory inspection readiness, in accordance with ... Development Plan. The CTC will provide support for critical day-to-day clinical study activities, including regulatory inspection readiness, in accordance with… more