Clinical Research Assistant II

MultiCare Health SystemTacoma, WA
$25 - $36

About The Position

Join a team that shares your calling At MultiCare, you’re more than just a job title — you’re part of a team built on trust that cares for each other, our patients and our communities. Belonging here means living our mission and values every day. If your purpose and passions align with ours, you’ll find a place to grow, do meaningful work and build a career you love in a community that feels like home. FTE: _.5, Shift: _Day, Schedule: _Part Time Position Summary The Research Assistant II is an ideal opportunity to support clinical research and health services research projects. Working in collaboration with the clinical research coordinator and study team, this position will aid with data, coordination and protocol. If you are seeking a role to support and advance your career in research, this might be an excellent fit for you.

Requirements

  • High school education required; Bachelor’s degree preferred
  • Valid health care provider CPR certification
  • Medical Assistant – Phlebotomy (must obtain within the first 90 days of employment)
  • Medical Assistant – Registered (must obtain within the first 90 days of employment)
  • Minimum two (2) years of related experience in healthcare or research (bench research, clinical research or health services research) OR one (1) year of healthcare experience plus one year of industry related research experience within a healthcare setting (such as working for MIRI)
  • Specific experience in clinical research with knowledge of clinical trials, informed consent design and process and conduct of clinical trials preferred
  • Highly proficient with MS Office (Word, Excel, Outlook), email, internet
  • Current Washington State Drivers License; and proof of a safe driving record (which meets established MHS Standards) obtained by a motor vehicle report from the appropriate state

Nice To Haves

  • Specific experience in clinical research with knowledge of clinical trials, informed consent design and process and conduct of clinical trials preferred

Responsibilities

  • You will distribute, collect and document essential data and aid in the compilation and verification of research data, samples, and/or specimens
  • You will coordinate and complete protocol related activities and research visits needed to complete research projects
  • You will aid in the identification and screening of patients
  • You will partner across internal and external groups applying leadership, good judgement and effective communication skills

Benefits

  • We provide a comprehensive benefits package, including competitive salary, medical, dental and retirement benefits and paid time off.
  • Competitive tuition assistance, award-winning residencies, fellowships and career development to invest in you.
  • Generous PTO, Code Lavender and Employee Assistance Programs to help you maintain balance and feel cared in your work and life.

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What This Job Offers

Job Type

Part-time

Career Level

Mid Level

Education Level

High school or GED

Number of Employees

1-10 employees

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