- Gilead Sciences, Inc. (Santa Monica, CA)
- …project teams to design and implement clinical studies. + Write protocols, investigator brochures, clinical study reports and review clinical trial documents + ... Conduct investigator meetings and lead site initiation visits with clinical...creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …safety signals. + Review documents supporting clinical development such as Investigator 's brochure, regulatory documents for IND/CTA, clinical sections of integrated ... lock and interim cuts. Supports site selection, patient recruitment, and investigator engagement through regular interactions and guidance. + Leads the analysis… more
- Taiho Oncology (Princeton, NJ)
- …and issues. + Oversee systems to track projects including all study, investigator and ethical review board information, patient recruitment activity, and financial ... specific requirements and industry standards. + Verify that the investigator follows the approved protocol, training and all GCP...$196,000 annually. This pay range is based on the market range for positions of this type. However, base… more
- Dana-Farber Cancer Institute (Boston, MA)
- …other Harvard Medical School-affiliated hospitals. Administrative: + Assists principal investigator with protocol development. + Assists principal investigator ... appropriate with the Institute's protocol review process. + Assists the principal investigator in developing the protocol budget. + Collaborates with the Dana-Farber… more
- Actalent (Lima, OH)
- …events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor. + Prescreen study candidates. + Obtain informed consent per ... other test results for completeness and alert values, ensuring investigator review in a timely fashion. + Discuss study...specialized experts who drive scale, innovation and speed to market . With a network of almost 30,000 consultants and… more
- Actalent (Tyler, TX)
- …trials at the site. + Work under the supervision of the Principal Investigator (s), exercising excellent clinical judgment in patient monitoring and care. + Maintain ... daily contact with the Principal Investigator (s) for recruitment activities, study start-up, and general communication....specialized experts who drive scale, innovation and speed to market . With a network of almost 30,000 consultants and… more
- Rush University Medical Center (Chicago, IL)
- …job-related experience and skills, as well as internal equity and industry specific market data. The pay range for each role reflects Rush's anticipated wage or ... studies, single site studies, intergroup studies, industry studies, and investigator initiated studies. Prepares internal and external regulatory submissions… more
- University of Pennsylvania (Philadelphia, PA)
- …performed, reporting adverse events and ensuring review and appropriate follow-up by investigator , monitoring patient care and treatment side effects in concert with ... with design, set-up and execute studies. Be responsible for writing investigator -initiated IND/IDE clinical trials in collaboration with faculty supervisor. Speak at… more
- Stanford University (Stanford, CA)
- …the close direction of the manager (CRM), regulatory specialist and principal investigator (s). The CRCII will support industry, federal and grant funded clinical ... define best practices. + Develop study budget with staff and principal investigator , identifying standard of care versus study procedures. Track patient and study… more
- University of Pennsylvania (Philadelphia, PA)
- …requirements, and (2) meet required obligations to patients/subjects, Principal Investigator (PI), study team and Sponsor/CRO. This position will report ... contribute to study-related meetings, including but not limited to Investigator Meetings, Site Initiation Visits, Intermediate Monitoring Visits, Close-out Visits,… more