- University of Pennsylvania (Philadelphia, PA)
- …of the initiation of Phase I-V clinical trials with a focus on required regulatory start - up approvals and associated site initiation documentation. Reporting ... maintain all regulatory affairs documentation/files as required. The Regulatory Affairs Start - Up Specialist is expected to resolve, with minimal… more
- University of Colorado (Aurora, CO)
- …and ensuring compliance with IRB consenting policies. + Direct and manage all regulatory study start - up , and maintenance activities ensuring that opening ... ** Regulatory and Compliance Program Director** **Description** **University of...Colorado Anschutz Medical Campus** **Department: Cancer Center** **Working Title: Regulatory and Compliance Program Director** **Position #:660200 - Requisition… more
- Rush University Medical Center (Chicago, IL)
- …lab staff. . Leads regular, timely meetings to track progress of study regulatory activities, including study start - up , maintenance, close-out activities; ... the circumstances of each case. **Summary:** The Clinical Research Regulatory Compliance Manager serves as the subject matter expert...of medical knowledge and improving patient outcomes. . Initiates start - up and training tasks for new study… more
- Houston Methodist (Houston, TX)
- …Harmonization (ICH). This position will work closely with the study teams for study start - up regulatory paperwork, maintain regulatory documents such as ... At Houston Methodist, the Regulatory Compliance Specialist position is responsible for coordinating...position is responsible for coordinating and performing study specific regulatory processes such as local IRB and external IRB… more
- University of Miami (Miami, FL)
- … Analyst II reviews, prepares, and provides oversight for initial and subsequent regulatory submissions from study start - up through study closure as ... well as the maintenance of regulatory documents to ensure compliance with applicable requirements and...the process of study submissions (initial and amendment) and regulatory document maintenance; serves as point of contact for… more
- University of Pennsylvania (Philadelphia, PA)
- …of the initiation of Phase I-V clinical trials with a focus on required regulatory start - up approvals and associated site initiation documentation. Reporting ... Summary Temporary Employee - Non-Exempt Job Description Ophthalmology seeks a part-time Regulatory Affairs Start - Up Specialist-CC to facilitate, with minimal… more
- Johns Hopkins University (Baltimore, MD)
- …**_Clinical Research Regulatory Specialist_** who will be responsible for managing regulatory start - up of clinical trials, assisting development of ... and continuing education trainings for the specific Urology Clinical Research Program. Regulatory start - up activities include site evaluation visits,… more
- Sanofi Group (Swiftwater, PA)
- …this role you will provide expert guidance on country and site selection strategies, regulatory considerations and start - up timelines, as well as patient ... and work to define the way of working and generating standardization among study start up team. + Recruitment and Screening: Assist with the creation and… more
- Vitalief (New Brunswick, NJ)
- …(for Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials); Regulatory work required for start - up documents; Processes related ... work for Industry, NIH, Cooperative Group, NCI and Investigator Initiated sponsored trials; Regulatory work for start - up document; Contract review and… more
- University of Miami (Miami, FL)
- …and/or Director of Regulatory with the day-to-day operations related to study start - up activities and regulatory maintenance of study records. CORE JOB ... SCCC has an exciting opportunity for a Full Time Regulatory Analyst 3 to work at the UHealth Medical...federal regulations. This process will take place from study start - up throughout the completion of the study.… more