- Abbott (Santa Clara, CA)
- …position will be required to execute their job responsibilities within the corporate policies and standard operating procedures. **What You'll Work On** + Design ... and Commercial Teams to support business priorities and serve as Clinical Science lead + Acts as lead scientist, project leader, or project contributor.… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- Otsuka Pharmaceutical Company is a global healthcare company with the corporate philosophy: "Otsuka-people creating new products for better health worldwide." Otsuka ... **(PK)** , **Pharmacokinetics-Pharmacodynamics (PK/PD)** and regulatory submissions. You will lead study design, execution and reporting of **clinical pharmacology**… more
- AbbVie (Irvine, CA)
- …toxin and aesthetic franchise scientific and business strategy. Responsibilities: + Lead with ownership the design and implementation of multiple aesthetic clinical ... training of investigators, study site personnel, and AbbVie study staff. + Lead global clinical study teams monitoring overall study integrity and review,… more
- AbbVie (San Francisco, CA)
- …analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. ... and efficacy of the molecule. As the SD Study Lead , is responsible for oversight of study enrollment and...other functions in these activities as required, consistent with corporate policies, to ensure that broad cross-functional perspectives are… more
- AbbVie (Irvine, CA)
- …analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses and ... other program documents. Lead development, validation, and justification of new clinical outcome...other functions in these activities as required, consistent with corporate policies, to ensure broad cross-functional perspectives are incorporated… more
- AbbVie (South San Francisco, CA)
- …of one or more clinical development programs. Participates in and may lead cross-functional teams to generate, deliver, and disseminate high-quality clinical data ... deliverables. Responsible for assessment and reporting of serious adverse events per corporate policy and regulations for those protocols on which assigned. +… more
- Bayer (San Diego, CA)
- …and/or Medical Affairs experience in multiple therapeutic areas; + Coordinates and lead TA updates, team discussions, training initiatives (ie journal clubs); + ... projects aligned with medical and brand strategy; including facilitating investigator -initiated research (IIR) and research site identification; + Responsible for… more
- AbbVie (Irvine, CA)
- …but not limited to clinical trials in Aesthetic Medicine. Participate and lead cross-functional teams to generate, deliver and interpret high quality research and ... design, analysis, interpretation, presentation and reporting of scientific protocols, Investigator Brochures, Clinical Study Reports, Clinician Reported Outcome Dossiers,… more