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Associate Director (Oncology)

Termin ważności:
2019-09-18 - 2020-01-31
Województwo / region:
Kraków, Wrocław, Katowice, dolnoslaskie
Firma:
ukryte


Your responsibilities: 

  • Controlling realization of the clinical research study,
  • Ensuring that assigned projects are delivered on time, within budget and with quality,
  • Communicate all critical issues, business growth opportunities, developing key relationships as well as providing input regarding budgeting discussions to drive productivity and quality within the region,
  • Preparing reports on the assigned activities according to the requirements, timelines and realization of study budget,
  • Ensure that clinical trials are conducted in compliance with the study protocol and all contractual agreements,
  • Taking part in teleconferences and meetings with services providers and team members from other departments,
  • Reporting to Head of Clinical Operations.


Requirements: 

  • Education: Minimum of a Bachelor of Science degree in scientific field,
  • Pharmaceutical or CRO background,
  • Excellent understanding of the drug development process,
  • Demonstrated ability to lead and manage staff,
  • Experience from leading trial teams and experience leading remote teams is an advantage,
  • Excellent oral and written communication skills in English,
  • Structured and well-organized way of work with attention to detail,
  • Experience writing Protocols and Clinical Study Reports,
  • Proficiency in GCP and ICH regulations.


We Offer: 

  • Motivating financial remuneration,
  • Numerous employee benefits,
  • Work in a supportive and highly professional team,
  • Further opportunities for professional development and career growth.

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