Clinical Affairs Director
Varian Medical Systems Inc
China, Beijing

About Varian

When you join Varian, you’re joining an organization with nearly $3 billion in annual revenue, and more than 6,500 team members across more than 30 countries.

You’ll be backed by a culture that is centered on fostering your creative potential, and experience the full support of an organization and leadership committed to inspiring you to do your best work.

Bring your talent to a place where your work will help fight cancer. Join Varian’s Oncology Systems team, and the work you do can make a difference by helping to create a world without fear of cancer.

We develop and manufacture products and solutions that innovate, support and streamline cancer-fighting solutions worldwide.

Our teams have a common drive to help others, and a passion for excellence. Join Varian and add your talent to the fight against cancer.

Job Description

Serve as the medical affairs representative in the APAC region

  • Manage Varian-sponsored clinical studies
  • Discuss potential investigator-initiated clinical research projects with customers
  • Manage investigator-initiated clinical research projects
  • Review clinical study protocols and reports
  • Work with researchers to develop abstract and journal article submissions
  • Make recommendations for clinical data and publications needed in the APAC region
  • Review and evaluate clinical grants applications
  • Meet with customers
  • Meet with regulatory bodies with APAC
  • Conduct literature searches
  • Analyze data from research studies, literature, and adverse event databases
  • Assist with wiring reports for regulatory submissions and other regulatory documentation
  • Serve as a resource to the company for information on clinical issues related to radiation therapy specific to the APAC region
  • Advocacy : meet with CFDA to discuss data requirements for new product approvals. Explain and convince CFDA reviewer regarding Varian's position
  • Interpret CFDA regulations and guidance documents and recommend how to meet CFDA requirements for running clinical studies and seeking product approvals
  • Establish and maintain relationships with high-level physicians, explore research opportunities and solicit feedback regarding Varian product
  • Scope of work :

  • Responsible for project planning and for executing in accordance with plan and budget
  • Work includes individual and team projects.
  • Minimum Requirements :

  • Advanced degree (e.g., MS, PhD, MD, DO) preferably in life sciences, health sciences, biomedical engineer, medical physics or equivalent degree / experiences.
  • Work included individual and team projects.
  • Skills, Abilities and other Requirement :

  • Excellent English language skills
  • Strong project management and organizational skills
  • Strong verbal and written skills
  • Strong critical thinking skills
  • Strong interpersonal skills
  • Preferences :

  • Experience with radiation therapy and / or oncology
  • Experience working in hospital environment
  • Experience within medical device industry
  • Experience with publishing in peer-reviewed literature
  • Job Condition

  • Requires domestic and international travel
  • Work involves visiting clinics where KV imaging and radiation therapy equipment is used
  • Work involves visiting surgical suites
  • Work may involve observing animal study procedures.
  • Occasional lifting of equipment (<15 Ibs)
  • Become part of our team

    At Varian, our culture is centered on fostering the creative potential of every employee through teamwork and collaboration.

    Our technologies touch millions of lives every day, and this inspires us to do our best work every day. By using your talent, ambition and creativity, you can build a career that allows you to make a real difference in people’s lives.

    You’re just one click away from the most impactful work you’ll ever do. Apply now and join our mission to help save lives.

    Someone, somewhere, will be glad you did.

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