Location:
Winter Park, FL
This is an exciting opportunity for an experienced Clinical Research Coordinator to take on a more influential role in the execution of clinical trials that advance modern medicine. In this position, you’ll work directly with patients and investigators while helping ensure studies are conducted with precision, integrity, and impact. It’s an ideal next step for a coordinator ready to deepen their expertise and grow within clinical research.
Why You Should Apply
-
Play a hands-on role in clinical trials that bring new therapies to patients
-
Take ownership of a growing study portfolio with increased responsibility
-
Collaborate closely with investigators, sponsors, and CRO partners
-
Build the skills and visibility needed to progress to a CRC III role
-
Salary and incredible incentive compensation
-
Strong benefit package including matching 401k, medical dental and weekly catered lunches!! Also, early out on Fridays
What You’ll Be Doing
-
Coordinating and managing day-to-day clinical trial activities
-
Guiding patients through informed consent, visits, and procedures
-
Conducting study visits including vitals, blood draws, ECGs, and specimen processing
-
Ensuring strict compliance with protocols, GCP, and ALCOA-C standards
-
Communicating with sponsors, CRAs, investigators, and clinic leadership
-
Supporting audits, monitoring visits, and study start-up activities
About You
-
Bachelor’s degree in psychology, biology, health sciences, or a related field
-
Strong knowledge of medical terminology and clinical research operations
-
Highly organized with excellent attention to detail
-
Professional, patient-focused, and able to work independently
-
Collaborative mindset with a positive, adaptable attitude
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to
tori@scientificsearch.com
and tell me why you’re interested. Or, feel free to email your resume. Please include
Job#19707
.