Medical Affairs Pharma / Drug Development

Medical Affairs Pharma / Drug Development

17 Jan 2024
California, Southsanfrancisco, 94080 Southsanfrancisco USA

Medical Affairs Pharma / Drug Development

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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 STUDIES
CLINICAL TRIAL
CLINICAL TRIALS
DATA CLEANING
FILING Additional Skills:
NEUROSCIENCE
PHARMACEUTICAL DEVELOPMENT
THERAPEUTIC

PLease email resume to Ellen at

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Job Details

  • ID
    JC8274147
  • State
  • City
  • Job type
    Contract
  • Salary
    Depends on Experience
  • Hiring Company
    CSI (Consultant Specialists Inc.)
  • Date
    2021-01-12
  • Deadline
    2021-03-13
  • Category

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