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Part Time Clinical Research Jobs (NOW HIRING)

$23.75 - $31.75/hr

Kristina Petersen's labin the Department of Nutritional Sciences is seekinga part-time Clinical Research Coordinator to support externally funded clinical trials investigating dietary interventions ...

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Part Time Clinical Research information

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

As of Aug 21, 2026, the average hourly pay for part time 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.

What is a part-time clinical research position?

A part-time clinical research position involves assisting with the planning, implementation, and monitoring of clinical trials or studies on a reduced or flexible schedule, typically less than 40 hours per week. These roles may include tasks such as data collection, patient recruitment, regulatory documentation, and supporting principal investigators. Part-time clinical research jobs are common in hospitals, universities, and pharmaceutical companies, and they offer opportunities for students, healthcare professionals, or individuals seeking flexible work arrangements.

What are some common challenges faced in part-time clinical research roles, and how can they be managed?

Part-time clinical research professionals often encounter challenges balancing project deadlines with limited working hours, as studies may require timely data collection and reporting. Effective communication with the research team and proactive scheduling can help ensure tasks are completed efficiently. Additionally, staying organized and regularly updating project management tools can aid in tracking progress and maintaining compliance with protocols. Building strong relationships with full-time staff also supports seamless collaboration and knowledge sharing across shifts.

What are the key skills and qualifications needed to thrive as a part time clinical research professional, and why are they important?

To excel as a Part Time Clinical Research professional, you need a foundational understanding of clinical research methods, data collection, and regulatory guidelines, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification are typically required. Attention to detail, strong organizational skills, and effective communication help you manage multiple tasks and collaborate with research teams. These competencies ensure accurate data handling, regulatory compliance, and the smooth execution of research studies.

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

AspectPart Time Clinical ResearchPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldRequires a bachelor's degree; certification as a CRC is common
Work EnvironmentResearch sites, hospitals, clinics, or pharmaceutical companiesResearch sites, hospitals, clinics, often overseeing study activities
Employer & Industry UsageUsed across research organizations, biotech, pharmaPrimarily employed by research sites and clinical trial sponsors
Common Search & ComparisonOften compared for entry-level roles in clinical researchCompared for roles involving study coordination and participant management

Part Time Clinical Research roles focus on supporting clinical studies, often involving data collection and patient interactions. Part Time Clinical Research Coordinators have additional responsibilities in managing study protocols and participant coordination. Both roles require relevant education and certifications, but Coordinators typically have more oversight duties.

More about Part Time Clinical Research jobs

What cities are hiring for Part Time Clinical Research jobs?

Cities with the most Part Time Clinical Research job openings:

What are the most commonly searched types of Clinical Research jobs?

The most popular types of Clinical Research jobs are:

What states have the most Part Time Clinical Research jobs?

States with the most job openings for Part Time Clinical Research jobs include:

Infographic showing various Part Time Clinical Research job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA โ€ข On-site

$53K - $58K/yr

Part-time

Re-posted 7 days ago


Job description

Job Type
Part-time
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

Salary Description
$53,000-$58,000