AD/Director, Clinical Scientist

Clinical ResearchClinical ResearchFull TimeRemoteTeam 51-200Company SiteLinkedIn

Location

United States

Posted

19 days ago

Salary

$181K - $213K / year

Postgraduate Degree3 yrs expEnglish

Job Description

• Support Medical Monitor or serve as clinical lead of a phase 1a/1b study and future late-stage studies, including contributing to/overseeing study start-up, enrollment, study medical monitoring, data cleaning, and CSR writing • Partner with investigators and CROs to design and implement clinical studies, respectively • Write protocols, investigator brochures, and clinical study reports, and review clinical trial documents • Conduct investigator meetings and safety review committee meetings and lead site initiation visits with clinical trial investigators • Execute and deploy drug development strategic plans, develop contingency plans, provide technical and strategic advice, and meet milestones and budgets • Translate findings from research and non-clinical studies into clinical development opportunities • Interact with clinical investigators and thought leaders • Conduct clinical trials using ethical guidelines relevant to the pharmaceutical industry, and ensure compliance with these external guidelines.

Job Requirements

  • PhD or Pharm D, with at least 3 years of oncology clinical development experience
  • Experience in all aspects of protocol conduct, both early and late phases, including protocol writing, start-up, study execution, analysis, and reporting
  • Deep commitment to understanding needs and improving the lives of patients, and a passion for developing novel therapeutics
  • Demonstrated ability to collaborate successfully with multiple functions in a team environment, including clinical operations, regulatory, and clinical pharmacology
  • Demonstrated record of accomplishment in a compressed time frame; capable of prioritizing tasks and delivering on deadlines with high-performance standards and attention to detail
  • Motivated to work in a fast-paced, high accountability, small company environment; a "can do" and collegial professional who leads through influence and interpersonal skills
  • Intellectually curious with the courage to challenge and seek new ways to improve work
  • Strong written and oral communication skills, including presentation skills
  • Ability to analyze and interpret data and develop written reports and presentations of those data
  • Solid critical, strategic, and analytical thinking skills
  • Travel (US and ex-US) required, to attend scientific conferences and study sites as needed.

Benefits

  • annual bonus
  • stock-based long-term incentives
  • medical, dental, and vision benefits
  • retirement
  • wellness stipend
  • flexible time off

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