Associate Research - Oncology

  • Full-time
  • Job Type: Full Time

Company Description

Henry Ford Health partners with millions of people on their health journey, across Michigan and around the world. We offer a full continuum of services from primary and preventative care to complex and specialty care, health insurance, a full suite of home health offerings, virtual care, pharmacy, eye care and other health care retail. With former Ascension southeast Michigan and Flint region locations now part of our team, Henry Ford's care is available in 13 hospitals and hundreds of ambulatory care locations. Based in Detroit, Henry Ford is one of the nation's most respected academic medical centers and is leading the Future of Health: Detroit, a $3 billion investment anchored by a reimagined Henry Ford academic healthcare campus.

Job Description

Assoc-Research-Clinical - Henry Ford Health

Job Title

Assoc-Research-Clinical

About the Department

Join the dynamic team at Providence Hospitals, a respected network within Henry Ford Health, serving communities across Oakland County. Our hospitals are known for advanced specialty care, deep local roots, and strong community connections. We combine the strength of a leading health system with the convenience of suburban locations and excellent amenities. As part of our team, you¿ll contribute to innovative research and clinical trials that drive medical advancements and improve patient outcomes.

Role Overview

As an Assoc-Research-Clinical, you will play a vital role in the design, administration, and monitoring of clinical trials. Your work will directly support research teams, investigators, and patients by ensuring the integrity and success of clinical studies. This role is essential in advancing medical knowledge and improving healthcare delivery across our network.

Why Henry Ford Health

At Henry Ford Health, we are relentless advocates for exceptional care for our patients, communities, and each other. We come to do meaningful work and grow our careers, and we stay for the connection, support, and shared pride in making the impossible, possible.

What You Will Do

  • Plan, organize, perform, and monitor daily project protocols.
  • Collect, prepare, and maintain essential research documentation, including informed consent records, case records, clinical notes, and medical reports.
  • Report and assist with managing protocol deviations, adverse events, and other project-related issues.
  • Assist with preparing and delivering internal and external presentations, conference reports, lectures, and publishing submissions.

 

Qualifications

What You Will Need

Required Qualifications

  • Understanding of the Food and Drug Administration (FDA) rules is beneficial.

Preferred Qualifications

  • None specified.

What We Offer

At Henry Ford Health, you'll find opportunities for career growth, collaboration with diverse teams, and the chance to engage in mission-driven work that makes a real difference. We foster a culture of continuous learning and innovation, empowering you to thrive in your role and contribute to our shared success.

Join Our Team

Ready to make an impact? Apply now and be part of a team that's transforming healthcare.

By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy apply

Privacy Notice