Clinical Trial Manager - Sponsor Office-Based in Melbourne

Client, AUS
23 Feb 2021
16 Mar 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Working with a leading Global pharmaceutical company (Clinical Project Manager)
Why Syneos Health? Join a game-changing global company that is reinventing the way therapies are developed and commercialized. With More than more than 24,000 employees worldwide we bring clinical and commercial minds together to create better, smarter, faster ways to get biopharmaceutical therapies to patients. Teaming with some of the most talented professionals in the industry, you'll gain exposure and work in a dynamic environment where you'll be supported with comprehensive resources including emerging technologies, data, science and knowledge sharing. Grow your career with a global company committed to shortening the distance from lab to life.

  • Project Manager or Snr Project Manager
  • Permanent Full-Time
  • Melbourne office-based at Pharma
  • Great company culture - certified Great Place To Work in Australia
  • Be part of a supportive and collaborative team within the FSP model
  • Competitive package and working with innovative CRO

  • Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance with GCP, relevant SOP's, and regulatory requirements.
  • Acts as a primary liaison between the Company and the Customer to ensure timely study launch, conduct, and closeout according to the Customer's and the Company's contractual agreement
  • Lead project team to ensure quality, timelines and budget management
  • Oversight for development and implementation of project plans
  • Plan, coordinate and present at internal and external meetings
  • Prepare project management reports for clients and management

  • Previous experience as a Project Manager working in clinical research or related relevant pharmaceutical industry experience
  • Bachelor's Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience
  • Clinical research organization (CRO) and relevant therapeutic experience preferred. Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements
  • Strong organizational skills
  • Strong ability to manage time and work independently
  • Direct therapeutic area expertise within Oncology is highly preferable
  • Ability to embrace new technologies.
  • Excellent communication, presentation, interpersonal skills, both written and spoken

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