University of Washington School of Public Health

Job Listing

Back to all Job Listings

Clinical Research Officer, Drug Development - PATH

Notice!This listing has expired and should not be applied for.
Location: Seattle, WA
Full-time position
Closing Date: open until filled
Job #11707
Posted: August 17, 2017
Description:

PATH is currently recruiting for a Clinical Research Officer to coordinate with the Drug Development program in Seattle/San Francisco to work in the Drug Development Group.

PATH is an international organization that drives transformative innovation to save lives and improve health, especially among women and children. We accelerate innovation across five platforms-vaccines, drugs, diagnostics, devices, and system and service innovations-that harness our entrepreneurial insight, scientific and public health expertise, and passion for health equity. By mobilizing partners around the world, we take innovation to scale, working alongside countries primarily in Africa and Asia to tackle their greatest health needs. Together, we deliver measurable results that disrupt the cycle of poor health.

PATH’s Drug Development Program (DRG) is working to develop and ensure availability and accessibility of safe and effective new medicines for diseases disproportionately affecting people in developing countries. By combining entrepreneurial energy, pharmaceutical expertise, and an innovative product development partnership model, we challenge the assumption that pharmaceutical research and development is too expensive to create the new medicines that the developing world desperately needs. 

Responsibilities:

  • Collaborates on the design of research studies and clinical trials, including the development of protocols, informed consent, and data collection tools.
  • Provides and/or oversees training of research staff.
  • Synthesizes input. 
  • Manages and develops project timelines, study budgets and tracking documents for management of study, site progress, and logistics.
  • Manages communications with regulatory bodies and internal and external ethics review committees, including new study applications, adverse event reporting, and protocol deviations. 
  • May collaborate with public or private sector partners, including academic and research organizations, to facilitate implementation of project objectives
  • Manages data collection, analysis, and reporting activities.
  • Leads and conducts qualitative and quantitative data analysis and/or conducts cost effectiveness analyses. 
  • Develops and approves study operating procedures and training materials.
  • Responsible for product regulatory submissions.
  • Performs site visits, as necessary.
Skills/Eligibility:

Required Skills

  • A minimum of 5 years’ experience in Global Health, Public Health, or Industry Clinical Research.
  • Master’s (or equivalent) in Public Health or similar.
  • Experience with clinical trial development and conduct.
  • Up to 10% domestic and 10% international.
  • Must have legal authorization to work in the United States.

 

How to Apply:

Click here to apply.

More Information