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Part Time Clinical Research Pharmaceutical Jobs (NOW HIRING)

The Pennsylvania State University

$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 ...

Uofl

$23.25 - $31/hr

A Temporary Clinical Research Coordinator is needed to coordinate clinical research studies ... pharmaceutical trials, hepatic arterial studies, and single- or multi-centered investigator ...

IQVIA

Clinical Research Coordinator

Sioux Falls, SD · On-site

$35 - $42/hr

On-site Schedule: Part-time (24 hours per week) Shape the Future of Medicine with IQVIA! Are you ... We partner with top pharmaceutical, biotechnology, and medical device companies to accelerate ...

IQVIA

Clinical Research Coordinator

Wichita, KS

$35 - $42/hr

On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced ... We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve ...

IQVIA

Clinical Research Coordinator

Albuquerque, NM

$35 - $42/hr

Onsite Schedule: 24 Hours/Week (Parttime) About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We collaborate with leading pharmaceutical ...

IQVIA

Clinical Research Coordinator

Jefferson City, MO

$35 - $42/hr

We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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

As of Aug 23, 2026, the average hourly pay for part time clinical research pharmaceutical 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 the difference between Part Time Clinical Research Pharmaceutical vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical Research PharmaceuticalPart Time Clinical Research Coordinator
CredentialsTypically requires a background in pharmacy, life sciences, or related fields; certifications like CCRP are commonRequires knowledge of clinical trial processes; certifications like CCRP are often preferred
Work EnvironmentPharmaceutical companies, CROs, or biotech firms; focus on drug development and testingResearch sites, hospitals, or clinics; focus on managing clinical trial activities
Employer & IndustryPharmaceutical industry, biotech firms, CROsResearch institutions, hospitals, clinical trial sites

While both roles involve clinical research, Part Time Clinical Research Pharmaceutical professionals focus on drug development and testing within pharmaceutical companies, whereas Part Time Clinical Research Coordinators manage and oversee clinical trial activities at research sites. The roles share similar certifications and work environments but differ in their primary focus and employer settings.

What cities are hiring for Part Time Clinical Research Pharmaceutical jobs?

Cities with the most Part Time Clinical Research Pharmaceutical job openings:

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

The most popular types of Clinical Research Pharmaceutical jobs are:

Part Time Clinical Research Pharmaceutical jobs near you

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA • On-site

$53K - $58K/yr

Part-time

Re-posted 10 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

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