ZipRecruiter

Log In

2

Clinical Trials Part Time Jobs in Florida (NOW HIRING)

UAB

CLINICAL RESEARCH RECRUITER (PART-TIME)

Tampa, FL · On-site

$15 - $24.40/hr

... (Part-Time). General Responsibilities * To recruit, schedule and perform follow-up with research ... Calls patients to enroll in clinical trials, enters participant data into the database, and emails ...

IQVIA

Clinical Trial Psych Rater

Coral Gables, FL · Remote

$62K - $156K/yr

Experience in CNS trials preferred. * Skills: * Strong interpersonal and communication skills for ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

next page

Showing results 1-20

All JobsClinical Trials JobsClinical Trials Part Time JobsClinical Trials Part Time Jobs in Florida

Clinical Trials Part Time information

What is a clinical trials part time job?

Clinical trials part time jobs are positions in which individuals assist with the planning, execution, or management of clinical research studies on a part-time basis. These roles may include research assistants, coordinators, data managers, or nurses, and offer flexible work hours to accommodate other commitments. Part-time staff are crucial in supporting the collection and management of data, participant recruitment, and ensuring compliance with study protocols. These positions are ideal for students, professionals seeking flexible hours, or those looking to gain experience in clinical research without committing to a full-time schedule.

What are the common responsibilities and challenges of working part-time in clinical trials?

Part-time roles in clinical trials typically involve supporting research coordinators, assisting with data collection and entry, participant recruitment, and ensuring compliance with study protocols. A common challenge can be balancing workload and communication with the team, as studies often require careful coordination and timely updates. Flexibility and strong organizational skills are important, as part-time staff may need to quickly adapt to changing priorities while maintaining high-quality standards. Despite these challenges, part-time positions offer valuable exposure to clinical research processes and can serve as a stepping stone to full-time roles or advanced positions in the field.

What are the key skills and qualifications needed to thrive in a part-time clinical trials role, and why are they important?

To thrive in a part-time clinical trials role, you typically need a background in life sciences or healthcare, attention to detail, and familiarity with clinical research protocols. Experience with electronic data capture (EDC) systems, knowledge of Good Clinical Practice (GCP), and sometimes certification such as SOCRA or ACRP are commonly required. Strong organizational skills, clear communication, and adaptability help you excel in coordinating studies and working with diverse teams. These skills ensure accurate data collection, regulatory compliance, and efficient support of clinical research objectives.

What is the difference between Clinical Trials Part Time vs Clinical Research Coordinator?

AspectClinical Trials Part TimeClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires a degree in health sciences or related field; often holds certifications such as CCRP or CCRC
Work EnvironmentPart-time roles in clinics, hospitals, or research facilities; flexible schedulesFull-time or part-time roles in research sites, hospitals, or pharmaceutical companies
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch sites, hospitals, pharmaceutical companies

Clinical Trials Part Time roles focus on supporting specific trial activities with flexible hours, while Clinical Research Coordinators oversee entire study processes, often working full-time. Both roles require similar credentials and are integral to clinical research, but differ mainly in scope and schedule.

What are the most commonly searched types of Clinical Trials jobs in Florida?

The most popular types of Clinical Trials jobs in Florida are:

Clinical Trials Part Time jobs near you
Infographic showing various Clinical Trials Part Time job openings in Florida as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution.

Clinical Research Physician - Part Time

Thermo Fisher Scientific

The Villages, FL • On-site

Part-time

Posted 29 days ago

Thermo Fisher Scientific rating

7.8

Company rating: 7.8 out of 10

Based on 429 frontline employees who took The Breakroom Quiz

170th of 545 rated manufacturers

Job description

Work Schedule
Other
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
Location/Division Specific Information:
Trialmed supports biopharmaceutical companies throughout the lifecycle of clinical trials. As a business of PPD, we are committed to optimizing each step in the patient journey and delivering best-in-class site performance to bring our customers greater certainty to clinical trial delivery.
*Must be legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check, which includes a drug screening.
Purpose:
Conducts clinical trials (studies) according to ICH GCP, local regulations, study protocols, and company processes as a principal investigator or sub-investigator. Ensures participant safety, protocol compliance, and data integrity through appropriate medical oversite. Collaborates with site leadership and cross-functional teams to support successful study execution, participant recruitment, enrollment, and retention.
  • Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and monitored for safety and adherence.
  • Attends Site Initiation Visits (SIV), Pre-Selections Visits (PSV) and Investigator meetings as required.
  • Initially functions as a Sub-Investigator and may assume Principal Investigator responsibilities based on study requirements, demonstrated performance, training completion, and site needs.
  • Supports participant recruitment and retention strategies through protocol expertise, community engagement, physician outreach, and collaboration with recruitment teams. Reviews enrollment progress, pre-screening and screening success rates, safety and retention of participants.
  • Interprets protocols and IB and participates in initiatives to strategize for patient recruitment.
  • Oversees management of investigational medical product (IMP).
  • Oversees multiple studies.
  • Cares for and protects the safety of participants through ethical conduct.
  • Fulfills and complies with all medical duties, ensuring that clinical trials are performed to acceptable medical, scientific and ethical standards.
  • Exercises meticulous attention to detail in recording information and source management.

Education and Experience:
  • MD or DO degree (or equivalent medical degree recognized in the country of practice) with at least 2 years working as a licensed physician. Neurologist are encouraged to apply.
  • Active, unrestricted medical license in good standing.
  • Exceptional general medical practitioner diagnosis and treatment proficiency.
  • A valid ICH GCP certificate (can be obtained after employment).
  • Prior clinical research experience is preferred but not required. Candidates should possess sufficient clinical expertise and medical judgment to safely conduct protocol-driven clinical research and oversee study participants. Strong clinical backgrounds seeking to transition into clinical research are encouraged to apply.
  • Demonstrated ability to collaborate effectively across a matrixed organization, partnering with clinical operations, recruitment, regulatory, pharmacy, laboratory, and sponsor-facing teams to achieve study objectives.

Knowledge, Skills, and Abilities:
  • Thorough understanding of medical terminology, drug safety, and interpretation of lab reports.
  • Working knowledge of scientific concepts related to the design and analysis of clinical trials.
  • Strong critical thinking, decision making, analytical and problem-solving skills.
  • Comprehensive attention to detail.
  • Capable of learning new processes and systems quickly.
  • Excellent communication, written, verbal and presentation skills.
  • Strong planning, organizational and project management skills.
  • Skilled in Word, Excel, PowerPoint and Internet use.

Working Conditions and Environment:
  • Work is performed in an office environment with exposure to electrical office equipment.
  • Occasional travel.

Physical Requirements:
  • Frequently stationary for 6-8 hours per day.
  • Repetitive hand movement of both hands.
  • Frequent mobility required.
  • Occasional crouching, stooping, bending and twisting.
  • Light to moderate lifting and carrying up to 15-20 lbs.
  • Ability to use a variety of computer software.
  • Ability to communicate information and ideas effectively, with the ability to listen to, and understand, information and ideas presented through spoken words and sentences.
  • Frequently interacts with others to obtain or relate information to diverse groups.
  • Ability to multitask and perform under stress.
  • Regular and consistent attendance.

What Thermo Fisher Scientific employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply