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Clinical Research Sponsorship Specialist

Il y a 2 mois

RueilMalmaison, Île-de-France PAR Fortrea France SARL Temps plein
Clinical Research Sponsorship SpecialistKey Responsibilities
  • Trial and Site Administration
  • Document Management
  • Regulatory and Site Start-Up Responsibilities
  • Budgeting, Agreement, and Payments
  • Meeting Planning

CORE Competency Expectations:

  • Fluent in Local Languages and Business Proficient in English (Verbal and Written) and Excellent Communication Skills
  • Good Understanding of Global, Country/Regional Clinical Research Guidelines and Ability to Work Within These Guidelines
  • Hands-on Knowledge of Good Documentation Practices
  • Good IT Skills (Use of MS Office, Use of Some Clinical IT Applications on Computer) and Ability to Adapt to New IT Applications. Strong MS Excel Skills Required
  • ICH-GCP Knowledge Appropriate to Role

At Fortrea, we are actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. We offer a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.