Job Details

ID #8464999
State California
City Southsanfrancisco
Job type Contract
Salary USD Depends on Experience Depends on Experience
Source CSI (Consultant Specialists Inc.)
Showed 2021-01-22
Date 2021-01-21
Deadline 2021-03-22
Category Et cetera
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Medical Affairs Pharma / Drug Development

California, Southsanfrancisco, 94080 Southsanfrancisco USA

Vacancy expired!

Position: Medical Director - Contractor

Job description:Client is recruiting a Medical Director who is a specialist in Stroke and/or Neuroscience. The role will be primarily based in South San Francisco within the Clinical Development Group (with online work while COVID precautions remain in place); responsible for the execution of late phase clinical trials. There will be the opportunity for travel and direct interaction, Your supervisor will be an experienced member of the development team. As an Medical Director in the Group you may:
    • Be an integral member, review, execute and provide input into Clinical Trial Medical Monitoring activities such as data cleaning, query follow up, interaction with sites and PI's, among others.
    • Support filing process for new molecules/indications
    • Collaborate in onboarding of new team members
    • Be involved in the design, execution, analysis and interpretation of data from clinical studies for molecules in development as well as marketed compounds.
    • Interact with globally recognized academic experts and clinical investigators
    • Participate in key clinical strategy, implementation and molecule management meetings in order to gain a deeper understanding of the complexities and challenges of medicines development
    • Provide clinical expertise in the stroke disease area for cross functional pharmaceutical development teams
    • Generate and present abstracts and oral presentations for key external conferences and other specialty meetings as well as publication opportunities.
    • Be involved in discussions and initiatives around Personalized Health Care (PHC) and patient selection for different therapeutic interventions
Skills: Substanial (3+ years) prior experience working in a clinical scientist role, preferably in the pharmaceutical industry, is required. Strong expertise with clinical trial data review with sufficient medical knowledge to independently review adverse event data is essential. Prior experience with oncology indications required, including familiarity with RECIST 1.1. Prior experience working with Genentech/Roche is a major plus. BA/BS in a biomedical field required MD or PHD required Skills and Experience:Required Skills: CLINICAL STUDIESCLINICAL TRIALCLINICAL TRIALSDATA CLEANINGFILING Additional Skills:NEUROSCIENCEPHARMACEUTICAL DEVELOPMENTTHERAPEUTIC PLease email resume to Ellen at

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