- Parexel (Sacramento, CA)
- …client in making budget and contractual decisions against the impacts to client clinical trial timelines + Follow client processes to develop, negotiate, track and ... execute global clinical study agreements with institutions and investigators participating in...study agreements with institutions and investigators participating in sponsored clinical trials + Work with partners to develop and… more
- Bristol Myers Squibb (San Diego, CA)
- … studies of radiopharmaceutical imaging agents. + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other ... design, and execution of Phase 0 to Phase 3 clinical trials, and medical monitoring. This role provides medical...clinical trial and regulatory documents + Conduct investigator meetings and lead site qualification and initiation visits… more
- Pfizer (South San Francisco, CA)
- …required + 4+ years' experience to include medical (eg patient care, clinical trial experience/ investigator , academic medicine, specialty training and/or board ... Working with other Pfizer functions engaged in benefit-risk management (Regulatory, Quality, Clinical , Medical, Corporate Audit, etc) to enable one medical voice +… more
- Humana (Sacramento, CA)
- …**Required Qualifications** + Bachelor's degree or equivalent work experience + Strong clinical experience to include multiple practice areas + At least 2 years ... **Preferred Qualifications** + Graduate degree and/or certifications (MBA, JD, MSN, Clinical Certifications, CPC, CCS, CFE, AHFI). + Understanding of healthcare… more
- Sumitomo Pharma (Sacramento, CA)
- … clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes ... clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contribute… more
- Genentech (South San Francisco, CA)
- …+ Drive timely formation and execution of high quality Phase IIIb/IV clinical trials and investigator -initiated research including study design, protocol ... to maintain an in-depth understanding of the medical strategy and relevant clinical and payer issues, while ensuring Genentech's partners understand key trends and… more
- BeOne Medicines (San Mateo, CA)
- …product lifecycle for the assigned project. + Provide CMC regulatory review for clinical protocols and investigator brochures, etc. for the assigned project. + ... Provide comments on new global guidance through company's commenting process. **Supervisory Responsibilities:** The position may or may not manage direct report(s). **Computer Skills:** Microsoft 360, Familiarity with Veeva is a plus. **Qualifications:** + 8+… more
- Parexel (Sacramento, CA)
- …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature ... comply with International Committee on Harmonization guidelines, Sponsor SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member,… more
- BeOne Medicines (Emeryville, CA)
- …and tactical/operational plans aligned to commercial and regulatory objectives. + Clinical trial patient and investigator recruitment experience + Validated ... **General Description:** As the Regional Strategic Feasibility Lead within Global Clinical Operations (GCO), you will play a vital role in collaboration with the… more
- Parexel (Sacramento, CA)
- …for a wide range of documents, including but not limited to investigator 's brochures, clinical study protocols and reports, integrated summaries, literature ... documents comply with International Committee on Harmonization guidelines, SOPs, Good Clinical Practices, and Good Publication Practices. As a study team member,… more