What are the responsibilities and job description for the Clinical Research Coordinator (Psychiatry/CNS) position at Protouch Staffing?
Location: Boynton Beach, FL
Job Type: Full-Time, Permanent
Schedule: Monday-Friday | 8:00 AM - 4:30 PM
Setting: Outpatient Clinical Research
Position Overview
We are seeking an experienced and motivated Clinical Research Coordinator (CRC) to join a growing outpatient clinical research team. This opportunity is ideal for a clinically experienced professional with prior research experience who is passionate about patient care, organization, and advancing medicine through clinical trials.
The ideal candidate will be bilingual in English and Spanish, possess strong clinical skills, and thrive in a fast-paced research environment. This role offers the opportunity to work closely with physicians, sponsors, and study participants while contributing to innovative Psychiatry/CNS research studies.
Responsibilities
Required
Interested candidates are encouraged to apply with an updated resume.
Kanika Kaintura
Healthcare Recruiter | Protouch Staffing
Email: kanika.kaintura@protouchstaffing.com
Phone: (972) 666-3992
Job Type: Full-Time, Permanent
Schedule: Monday-Friday | 8:00 AM - 4:30 PM
Setting: Outpatient Clinical Research
Position Overview
We are seeking an experienced and motivated Clinical Research Coordinator (CRC) to join a growing outpatient clinical research team. This opportunity is ideal for a clinically experienced professional with prior research experience who is passionate about patient care, organization, and advancing medicine through clinical trials.
The ideal candidate will be bilingual in English and Spanish, possess strong clinical skills, and thrive in a fast-paced research environment. This role offers the opportunity to work closely with physicians, sponsors, and study participants while contributing to innovative Psychiatry/CNS research studies.
Responsibilities
- Coordinate and manage clinical research studies across multiple therapeutic areas.
- Conduct patient visits and perform study-related procedures, including vital signs, ECGs, phlebotomy, lab processing, and specimen handling.
- Recruit, screen, and enroll study participants.
- Maintain accurate source documentation and timely data entry.
- Ensure protocol compliance and adherence to Good Clinical Practice (GCP) guidelines.
- Communicate effectively with sponsors, CROs, vendors, investigators, and study participants.
- Assist with regulatory documentation and study start-up activities.
- Manage study schedules, patient follow-ups, and visit coordination.
- Support high-quality patient care and research excellence.
Required
- Prior clinical research experience.
- Prior hands-on clinical experience, including phlebotomy, ECGs, and vital signs.
- Bilingual in English and Spanish.
- Strong knowledge of medical terminology and clinical laboratory procedures.
- Understanding of GCP guidelines and FDA regulations.
- Excellent organizational, communication, and multitasking skills.
- MA, LPN, or RN certification/licensure.
- Experience with EMR systems.
- Experience with EDC systems, eSource, and clinical research documentation.
- Medical Insurance
- Dental Insurance
- Vision Insurance
- 401(k) Retirement Plan
- Career Growth Opportunities
- Supportive and Collaborative Team Environment
- Opportunity to Work on Cutting-Edge Clinical Trials
- Full-Time Position
- Adult and Geriatric Patient Population
- Typical Patient Volume: Approximately 3-8 patients per day, depending on study protocols
- Occasional Weekend Flexibility Preferred
- Multiple Openings Available
Interested candidates are encouraged to apply with an updated resume.
Kanika Kaintura
Healthcare Recruiter | Protouch Staffing
Email: kanika.kaintura@protouchstaffing.com
Phone: (972) 666-3992
Salary : $25 - $36