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Weekend Research Jobs in Boca Raton, FL (NOW HIRING)

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

GNP Research

Clinical Research Coordinator

Cooper City, FL

$22.25 - $29.50/hr

GNP Research is seeking an experienced Clinical Research Coordinator (CRC) to lead and manage clinical trials across various therapeutic areas. The ideal candidate is detail-oriented, proactive, and ...

Research Centers of America

Research Assistant I

Hollywood, FL · On-site

$17.50 - $24.25/hr

CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver ...

Research Centers of America

Research Assistant I

Hollywood, FL · On-site

$17.50 - $24.25/hr

CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver ...

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All JobsWeekend Research JobsWeekend Research Jobs in Boca Raton, FL

Weekend Research information

What is a Weekend Research job?

A Weekend Research job typically involves conducting research tasks during weekends, which can include data collection, literature reviews, experiments, or analysis depending on the field. These roles are often part-time and may be suited for students, professionals seeking extra income, or those unable to work during regular weekday hours. Weekend research positions can be found in academic institutions, private companies, or independent projects. Responsibilities and requirements vary by employer, but attention to detail, strong organizational skills, and the ability to work independently are usually important.

What are some common challenges faced by Weekend Research professionals, and how can they effectively manage their workload?

Weekend Research professionals often face the challenge of balancing tight deadlines and limited access to colleagues or resources during non-standard hours. To manage these challenges, it’s important to plan tasks ahead, utilize digital collaboration tools, and communicate clearly with team members about progress and needs before the weekend. Additionally, setting clear objectives and prioritizing tasks can help ensure efficient use of time, allowing for thorough and high-quality research even when support is limited.

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

To thrive as a Weekend Researcher, you typically need strong analytical skills, attention to detail, and a relevant academic background or experience in research methods. Familiarity with data analysis tools, online research databases, and citation management systems is often required. Excellent time management, self-motivation, and clear written communication make someone stand out in this position. These skills and qualities are essential for producing accurate, timely, and well-organized research findings, especially within tight weekend deadlines.
What are the most commonly searched types of Research jobs in Boca Raton, FL? The most popular types of Research jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Weekend Research jobs? Cities near Boca Raton, FL with the most Weekend Research job openings:
Weekend Research jobs near you
Infographic showing various Weekend Research job openings in Boca Raton, FL as of June 2026, with employment types broken down into 2% Locum Tenens, 2% As Needed, 59% Full Time, 34% Part Time, and 3% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

Clinical Research Coordinator

Headlands Research

Lake Worth, FL

$21.50 - $28.75/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago

Job description

Clinical Research Coordinator (CRC)

Location: Lake Worth, FL | Site Name: JEM Research Institute | Full-Time

Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Lake Worth, FL. The CRC will manage and execute Phase II-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.

Type:  Regular Full-time Employee
Schedule:  Mondays through Fridays, 8:30am - 4:30pm
Location:  Onsite in Lake Worth, FL (no capabilities for remote or hybrid work)
Reports to:  Clinical Research Manager
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes
 Why Join Us?

You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.

Responsibilities:

  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out
  • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
  • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
  • Manage subject recruitment, informed consent, and retention strategies
  • Ensure timely data entry and resolution of EDC queries
  • Report and follow up on all adverse events, serious adverse events, and deviations
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
  • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Requirements:

  • Required: High school diploma or GED
  • Experience:
    • Minimum of 1 year of experience as a Clinical Research Coordinator OR
    • Minimum of 2 years of experience as a Research Assistant in Clinical Research
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
  • Proficiency in medical terminology and clinical documentation practices
  • Strong interpersonal, verbal, and written communication skills
  • Organized, detail-oriented, and capable of managing multiple priorities
  • Proficient in Microsoft Office and other clinical research systems
  • Bilingual (English/Spanish) is strongly preferred

Apply now to become a part of a team that's changing the future of healthcare-one trial at a time.

Apply