- Parexel (Sacramento, CA)
- …+ Ability to work on complex tasks requiring in-depth evaluation + Good knowledge of drug safety and the drug development process + Ability to exercise ... documents, data handling conventions, client's guidelines and procedures, and global drug safety regulations and guidelines + Maintaining an awareness of global… more
- Parexel (Sacramento, CA)
- …as contracted across multiple channels and interactions such as: --Consultancy on protocol development , drug development program etc. --Medical review of ... but not essential - A background in clinical aspects of drug development , including all aspects of Medical Monitoring and study design/execution, preferred… more
- Parexel (Sacramento, CA)
- …with specialized therapeutic expertise and some experience across indications, clients and drug development . They initiate and maintain medical and consultative ... and will be manifested in high quality consultation on protocol development or drug development programs, medical review of various documents, collaboration… more
- Pfizer (San Diego, CA)
- …side of the sponsor leading studies Experience in or strong understanding of Oncology Drug Development especially in Early Development Strong knowledge of ... POSITION SUMMARY You will lead and coordinate the development of multiple studies of novel biological and...medical leave, and health benefits to include medical, prescription drug , dental and vision coverage. Learn more at Pfizer… more
- BeOne Medicines (San Mateo, CA)
- …**Supervisory Responsibilities:** + Demonstrates knowledge of global clinical trials and the drug development process. + Experience in vendor oversight and ... **General Description:** The Manager of Clinical Supply Chain manages drug supply activities related to planning, label development... drug supply activities related to planning, label development , label & pack, and distribution for one or… more
- Parexel (Sacramento, CA)
- …ability to learn relevant Client Therapeutic Areas. + Basic understanding of the drug development process. + Good understanding of Clinical Study Management ... timelines. + Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for… more
- BeOne Medicines (San Mateo, CA)
- …degree and 12+ years or Masters degree and 8+ years in clinical or drug development in the biotech/pharmaceutical/CRO industry or the relevant clinical research ... clinical operations strategy in line with Biotech Unit asset development strategy + Within Biotech Unit, make recommendations in...such as IB, ICF, DSUR + Ensure timely clinical drug supply + Oversee and ensure feasibility, study start-up,… more
- Parexel (Sacramento, CA)
- …ability to learn relevant Client Therapeutic Areas. + Basic understanding of the drug development process. + Good understanding of Clinical Study Management ... timelines. + Manages study supplies (Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site. Prepares study drug for… more
- Parexel (Sacramento, CA)
- …techniques and interpret results + Familiarity with regulatory/research guidelines on drug development , GCP, and statistical principles (especially ICH ... + Provide broad statistical support, including trial design, protocol and CRF development on specific studies + Lead production and quality control of randomization,… more
- Parexel (Sacramento, CA)
- At **Parexel** , we don't just support drug development -we help shape it. As a **Senior/Vice President, Technical** on our Regulatory Strategy (RS) team, you'll ... draw upon their wealth of experience in clinical trial design and drug development to join Parexel's highly recognized Regulatory Strategy team! A Senior/Vice… more
