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Study Com Jobs in Florida (NOW HIRING)

Showing results 21-40

Study Com information

See Florida salary details

$16.4K

$93.6K

$153.9K

How much do study com jobs pay per year?

As of Aug 16, 2026, the average yearly pay for study com in Florida is $93,628.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,500.00 and $117,300.00 per year, depending on experience, location, and employer.

What is the difference between Study Com vs Study Coordinator?

AspectStudy ComStudy Coordinator
Required CredentialsTypically a bachelor's degree, sometimes certifications in clinical researchUsually a bachelor's degree, often with certifications like CCRP or CCRC
Work EnvironmentOffice-based, research institutions, hospitalsClinical settings, hospitals, research sites
Employer & Industry UsageResearch organizations, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Common Search & ComparisonOften compared for roles in clinical research teamsFrequently compared with Study Com as a supporting role

Study Coordinators and Study Com roles both support clinical research but differ mainly in scope and responsibilities. Study Coordinators typically handle day-to-day trial management, patient coordination, and data collection, while Study Com may focus on broader communication and administrative tasks within research projects. Both roles require relevant certifications and work in similar environments, making them closely related in the clinical research industry.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and project management, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as CCRC or CCRP is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating between study teams, participants, and regulatory bodies. These competencies ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, which is vital for research integrity and successful trial outcomes.

What are the typical responsibilities of a study coordinator in a clinical research setting?

A Study Coordinator, often referred to as a Clinical Research Coordinator, is responsible for managing daily operations of clinical trials. This includes recruiting and screening study participants, obtaining informed consent, scheduling and conducting study visits, collecting and recording data, and ensuring compliance with regulatory requirements. Coordinators also act as a liaison between investigators, sponsors, and study participants, making strong organizational and communication skills essential. The role offers opportunities to learn about various aspects of clinical research, paving the way for career advancement into project management or regulatory affairs.

What is a study com?

Study.com jobs refer to employment opportunities with Study.com, an online education platform that provides video lessons, study guides, and other educational resources. Job roles at Study.com can include content writers, curriculum developers, video editors, software engineers, and customer support specialists. Employees work to create and maintain high-quality educational content and ensure a positive learning experience for users. Some positions are remote or freelance, offering flexible work options. Working at Study.com can be a good fit for those passionate about education and technology.

What are popular job titles related to Study Com jobs in Florida?

For Study Com jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Study Com jobs?

Cities in Florida with the most Study Com job openings:

Infographic showing various Study Com job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, 1% Temporary, and 5% Contract. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $93,628 per year, or $45 per hour.

Clinical Research Coordinator (Psychiatry/CNS)

Protouch Staffing

Boynton Beach, FL

$25 - $36/hr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 13 days ago


Job description

Clinical Research Coordinator (Psychiatry/CNS)

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
  • 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.

QualificationsRequired
  • 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.

Preferred
  • MA, LPN, or RN certification/licensure.

  • Experience with EMR systems.

  • Experience with EDC systems, eSource, and clinical research documentation.

Benefits
  • 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

Additional Information
  • 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

How to Apply

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


Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989