- Parexel (Topeka, KS)
- …with data from study sites as per required timelines. + Manages study supplies ( Investigator Site File (ISF), etc.), drug supplies and drug accountability ... visit reports in CTMS and provides timely feedback to the Principal Investigator , including follow-up letter, within required timelines and in line with Client… more
- Parexel (Baton Rouge, LA)
- …documents, data handling conventions, client's guidelines and procedures, and global drug safety regulations and guidelines + Maintaining an awareness of global ... judgement)), clinical trial, and literature cases including combination products { drug -device}) according to client/Parexel Standard Operating Procedures (SOPs; as… more
- Parexel (Cheyenne, WY)
- …the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance ... The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (eg… more
- Parexel (Baton Rouge, LA)
- …the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance ... The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (eg… more
- BeOne Medicines (Emeryville, CA)
- …concepts, synopses, protocols, and amendments + Informed consent documents + Investigator Brochures + Clinical study reports + Abstracts, posters and manuscripts ... Update Reports + Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports + Risks / benefits analysis for applicable… more
- BeOne Medicines (Emeryville, CA)
- …to oncology. ? Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing. ? High level ... concepts, synopses, protocols, and amendments ? Informed consent documents ? Investigator Brochures ? Clinical study reports ? Abstracts, posters and manuscripts… more
- Organon & Co. (Chicago, IL)
- …and research including facilitation of research collaborations such as investigator -initiated trials and collaboration with Clinical Development colleagues on ... investigator selection, relationship, and site performance/recruitment. + Assist in...and medical leave, and health benefits including medical, prescription drug , dental, and vision coverage in accordance with the… more
- Parexel (St. Paul, MN)
- …looking to leverage their clinical expertise in the dynamic field of clinical drug development. As a medical expert and strategic partner, you'll play a pivotal ... medical and protocol-related questions from sites and study teams **Shape Drug Development Strategy** + Participate in early engagement activities and feasibility… more
- SLAC National Accelerator Laboratory (Menlo Park, CA)
- …Make recommendations on experimental design and/or research direction to principal investigator . + Independently conduct complex (lab and/or field) experiments to ... conferences. + Oversee supply and equipment budget under supervision of principal investigator or business manager. + Work with health and safety department to… more
- National Renewable Energy Laboratory (Golden, CO)
- …the technical leader for the ARIES Cyber Range as well as the principal investigator for other large projects and programs + Drives proposal strategy, identifies new ... Directive 12 (HSPD-12), which includes a favorable background investigation. ** Drug Free Workplace** NLR is committed to maintaining a... Free Workplace** NLR is committed to maintaining a drug -free workplace in accordance with the federal Drug… more
- Stony Brook University (Stony Brook, NY)
- …work. ? Experience in mouse tumor models. ? Experience in drug delivery. ? Experience in immunostaining and confocal microscopy. **Preferred Qualifications:** ... ? Extensive experience in peptide-based or micro-robots drug delivery systems. ? Demonstration of scholarship in pharmaceutical science equivalent to level of study,… more
- Parexel (Cheyenne, WY)
- …therapeutic expertise and some experience across indications, clients and drug development. They initiate and maintain medical and consultative relationships ... will be manifested in high quality consultation on protocol development or drug development programs, medical review of various documents, collaboration on internal… more
- Arvinas (New Haven, CT)
- …tumors with KRAS G12D mutations. On August 8 th 2025, the US Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an ... This training opportunity allows the individual to learn the process of early drug discovery in a collaborative environment. This position reports to a Senior… more
- BeOne Medicines (Emeryville, CA)
- …per the study TMF QC plan + Provides input to Global Clinical Supplies regarding drug inventories in region and reviews local drug labels for region. Provides ... regional study budgets + Works closely with Clinical Business Operation on investigator fees, site payment issues and patient travel reimbursement activities +… more
- Teleflex (Minneapolis, MN)
- …System. Teleflex's product portfolio now also includes Passeo-18 Lux Peripheral Drug -Coated Balloon Catheter, Pantera Lux Drug -Coated Balloon Catheter, Orsiro ... department systems and development initiatives including related trainings. - Support investigator meetings as needed. - Support Protocol Deviation and Adverse Event… more
- Parexel (Little Rock, AR)
- …to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final ... and Experience** : + Demonstrated understanding of clinical research, the drug development process, and industry guidelines and regulations, eg, ICH-GCP. +… more
- Caris Life Sciences (Irving, TX)
- …Requirements** + This role requires frequent travel to scientific conferences, investigator meetings, customer engagements, and internal leadership meetings. + Some ... must successfully complete pre-employment process, which includes criminal background check, drug screening, credit check ( applicable for certain positions) and… more
- BeOne Medicines (San Mateo, CA)
- …per the study TMF QC plan + Provides input to Global Clinical Supplies regarding drug inventories in region and reviews local drug labels for region. Provides ... regional study budgets + Works closely with Clinical Business Operation on investigator fees, site payment issues and patient travel reimbursement activities +… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** The Senior Investigator of Deviations Management for Drug Substance Manufacturing (DSM) is responsible to complete major and complex ... North America's largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.… more
- Adams County Government (Brighton, CO)
- Medicolegal Death Investigator I Print (https://www.governmentjobs.com/careers/adams/jobs/newprint/5188460) Apply Medicolegal Death Investigator I Salary ... Questions What Success Looks Like In This Job The Medicolegal Death Investigator /Deputy Coroner is primarily responsible for the investigation of unexpected,… more
