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Part Time Icon Clinical Research Jobs (NOW HIRING)

Main Line Health

Clinical Research Coord II

Wynnewood, PA · Hybrid

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator II Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Main Line Health

Clinical Research Coord II

Wynnewood, PA · On-site

$23.25 - $31/hr

This position is eligible for up to $6,000 per year based upon your Full or Part Time status ... Clinical Research Coordinator II Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

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Part Time Icon Clinical Research information

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How much do part time icon clinical research jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for part time icon clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

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

AspectPart Time Icon Clinical ResearchPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldRequires a bachelor's degree, often in health sciences, with some roles preferring certification
Work EnvironmentConducts clinical trials, often in research facilities or hospitalsManages daily trial activities, interacts with patients and research teams
Employer & Industry UsageUsed by pharmaceutical companies, research organizations, hospitalsCommonly employed by research sites, hospitals, and clinical trial sponsors

Part Time Icon Clinical Research and Part Time Clinical Research Coordinator roles share similar credentials and work environments, focusing on supporting clinical trials. The main difference lies in their specific responsibilities, with Icon roles often emphasizing trial support and coordination, while Clinical Research Coordinators handle more direct patient interactions and trial management tasks.

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Part Time Icon Clinical Research jobs near you
Infographic showing various Part Time Icon Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.

Part Time Clinical Research Coordinator

SerenaGroup Inc

Monroeville, PA

$24 - $32/hr

Part-time

Re-posted 20 days ago

Job description

Description

The Clinical Research Coordinator (CRC) at SerenaGroup plays a critical role in the execution of clinical trials focused on advanced wound care and hyperbaric medicine. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory guidelines, and supporting high-quality patient care and data integrity throughout the study lifecycle.


The CRC will work collaboratively with Principal Investigators, Clinical Trial Leads, sponsors, and cross-functional teams to ensure studies are conducted efficiently, ethically, and in alignment with SerenaGroup's commitment to evidence-based care and improved patient outcomes.

Key Responsibilities


Study Coordination & Execution

  • Coordinate and manage day-to-day clinical trial activities from study start-up through close-out 
  • Schedule and conduct study visits in accordance with protocol requirements 
  • Ensure proper informed consent is obtained and documented for all study participants 
  • Maintain accurate and up-to-date study documentation, including regulatory binders and source documents 

Patient Care & Engagement

  • Identify, recruit, and screen eligible patients for clinical trials 
  • Educate patients on study protocols, procedures, and expectations 
  • Monitor patient safety and report adverse events in accordance with regulatory requirements 

Data Management & Compliance

  • Accurately collect, record, and enter study data into electronic data capture (EDC) systems 
  • Perform source data verification (SDV) and ensure data integrity and completeness 
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, and SerenaGroup SOPs 

Collaboration & Communication

  • Serve as a liaison between investigators, sponsors, CROs, and internal teams 
  • Support monitoring visits, audits, and regulatory inspections 
  • Communicate effectively with cross-functional teams to ensure study milestones are met 

Qualifications


Education & Experience

  • Bachelor's degree in life sciences, healthcare, or related field preferred 
  • 1-3 years of experience in clinical research or healthcare setting (wound care experience a plus) 
  • Experience working with clinical trial protocols and regulatory requirements preferred 

Skills & Competencies

  • Strong organizational and time management skills 
  • High attention to detail and accuracy in documentation 
  • Excellent interpersonal and communication skills 
  • Ability to manage multiple studies and priorities in a fast-paced environment 
  • Proficiency in EDC systems and Microsoft Office Suite 

Preferred Qualifications

  • Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA) 
  • Experience in wound care, hyperbaric medicine, or related therapeutic areas 
  • Familiarity with clinical trial start-up and regulatory submissions  

Apply