- Cedars-Sinai (Los Angeles, CA)
- …we strive for. **Join our team and contribute to groundbreaking research.** The Research Associate II works at a high level of excellence and commitment to perform a ... successful management and administration of essential regulatory documents. The Research Associate II is responsible for ensuring timely submission of complete,… more
- Bristol Myers Squibb (Brisbane, CA)
- …DSURs, etc. + Co-lead the cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments ... and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more
- AbbVie (North Chicago, IL)
- …timely documentation at the study level to drive for timely execution of clinical trial (s) + Vendor management, including Request for Proposal (RFP)/initiation, ... submissions, patient reported outcome measures, study execution plan, informed consent, site budgets and agreements, clinical study report, training materials,… more
- ICON Clinical Research (Lenexa, KS)
- …and essentially making sure the study participants are healthy eNugh to participate in the clinical trial according the protocol of a study. **What you will be ... Medical Research Associate - PRN - (Onsite) Lenexa, KS ICON...KS ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive… more
- Catalent Pharma Solutions (Kansas City, MO)
- …stand-alone and integrated biologics projects._ The Kansas City **Supply Chain Distribution Associate II** supports clinical trial projects through ... **Distribution Associate II** **Position Summary:** + **Work Schedule:** M-F...accurately picking and packing clinical site and depot shipments; providing warehouse support to the… more
- Xeris Pharmaceuticals, Inc. (Chicago, IL)
- …degree in biostatistics, statistics, or epidemiology + A minimum of six years of clinical trial experience as a statistician and/or statistical programmer in the ... **Overview** The Associate Director, Biostatistics and Statistical Programming will drive...to study design, protocol development, case report form development, clinical study reports, and exhibits for other reports and… more
- Baylor Scott & White Health (Dallas, TX)
- **JOB SUMMARY** The Clinical Research Regulatory Specialist supports clinical research activities through the development of protocol-specific documents and ... This position also provides regulatory guidance and direction to internal clinical research programs to ensure compliance with all applicable policies, procedures… more
- UCLA Fielding School of Public Health (Los Angeles, CA)
- …call will be shared between providers. This clinic has a robust clinical trial program including access to on site phase I trials. Clinic website ... at UCLA is seeking physicians in the Health Sciences Clinical Professor series at the Instructor, Assistant, Associate... Clinical Professor series at the Instructor, Assistant, Associate , or full Professor ranks for the San Luis… more
- Catalent Pharma Solutions (San Diego, CA)
- …and performance of production audits in a Class 100,000 environment, maintenance of clinical trial material inventory logs + Other duties as assigned **The ... **Quality Assurance (QA) Associate I, Manufacturing** **Position Summary:** Catalent, Inc. is...manufacturing and stability storage and testing as well as Clinical Supply Services. At Catalent San Diego, we recruit… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking a highly motivated Associate Director (AD) to join the Quantitative Pharmacology (QP) group. The AD will lead model-informed drug development ... combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.… more