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Part Time Weekend Clinical Research Jobs (NOW HIRING)

Clinical Research Coord I

Wynnewood, PA

$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 I Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

Clinical Research Coord I

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 I Shift: 8am-4:30p and variable, Monday-Friday Flexibility required ...

$23.25 - $31/hr

This is a part time temporary position scheduled to work 15 hours per week. Essential Duties and Responsibilities: * Facilitates compliance with the research protocol and Good Clinical Practice ...

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 Weekend Clinical Research information

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

As of Aug 13, 2026, the average hourly pay for part time weekend clinical research in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.
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What cities are hiring for Part Time Weekend Clinical Research jobs? Cities with the most Part Time Weekend Clinical Research job openings:
What are the most commonly searched types of Weekend Clinical Research jobs? The most popular types of Weekend Clinical Research jobs are:
What states have the most Part Time Weekend Clinical Research jobs? States with the most job openings for Part Time Weekend Clinical Research jobs include:
Infographic showing various Part Time Weekend Clinical Research job openings in the United States as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Part Time Clinical Research Coordinator

SerenaGroup, Inc

Monroeville, PA • On-site

$24 - $32/hr

Part-time

Re-posted 3 hours 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
Requirements: