Memorial Healthcare·Pembroke Pines, Florida
Coordinates the implementation of multiple clinical research studies, focusing on IRB submissions for phase 1-4 trials and regulatory compliance. Manages sponsor visits, adverse events, and the training of junior clinical research coordinators.
At Memorial, we are dedicated to improving the health, well-being and, most of all, quality of life for the people entrusted to our care. An unwavering commitment to our service vision is what makes the difference. It is the foundation of The Memorial Experience.
Coordinates and assists with the implementation of multiple clinical research studies.
Candidates with Oncology Regulatory clinical research experience highly preferred.
Accountability, accuracy, clinical research - Regulatory compliance, customer service, develops relationships, effective communication, research - Reporting, responding to change, standards of behavior
Education and Certification Requirements: High School Diploma or Equivalent (Required)
Requires critical thinking skills, effective communication skills, decisive judgment and the ability to work with minimal supervision. Demonstrates ability to work effectively as a team member. Ability to multi-task.
Required
Work
Experience: Two (2) years of clinical research experience required.
This job description is not intended, nor should it be construed to be an exhaustive list of all responsibilities, skills, efforts or working conditions associated with the job. It is intended to indicate the general nature and level of work performed by employees within this classification.
Wages shown on independent job boards reflect market averages, not specific to any employer. We encourage candidates to talk to their Memorial Healthcare System recruiter to discuss actual pay rates, during the hiring process.
Memorial Healthcare System is proud to be an equal opportunity employer committed to workplace diversity.
Memorial Healthcare System recruits, hires and promotes qualified candidates for employment opportunities without regard to race, color, age, religion, gender, gender identity or expression, sexual orientation, national origin, veteran status, disability, genetic information, or any factor prohibited by law.
We are proud to offer Veteran’s Preference to former military, reservists and military spouses (including widows and widowers). You must indicate your status on your application to take advantage of this program.
Employment is subject to post offer, pre-placement assessment, including drug testing.
If you need reasonable accommodation during the application process, please call 954-276-8340 (M-F, 8am-5pm) or email TalentAcquisitionCenter@mhs.net [TalentAcquisitionCenter@mhs.net]
Market context
In Florida, oncology regulatory research coordinator roles are typically driven by active cancer research programs and the need to keep studies compliant and moving on schedule. These positions are competitive because employers often look for clinical research experience plus oncology-specific regulatory knowledge; this role requires a high school diploma or equivalent and at least two years of clinical research experience, with oncology regulatory research highly preferred. Review the AI-summarized requirements and benefits here to save time, then tailor your application to highlight regulatory coordination, protocol support, and oncology exposure.
