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Parttime Clinical Research Rater Jobs in Pennsylvania

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 ...

Main Line Health

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 ...

Main Line Health

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 ...

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 ...

The Pennsylvania State University

$21/hr

AND POSITION REQUIREMENTS EPCSE is seeking a Part Time Clinical Supervisor. The primary job ... research, and service mission. Federal Contractors Labor Law Poster PA State Labor Law Poster Penn ...

IQVIA

Site Research Assistant

Pittsburgh, PA · On-site

$25 - $39/hr

Parttime, 24 hours per week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to transforming healthcare. We partner with ...

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Parttime Clinical Research Rater information

What is the difference between Parttime Clinical Research Rater vs Parttime Clinical Research Coordinator?

AspectParttime Clinical Research RaterParttime Clinical Research Coordinator
CredentialsTypically requires a high school diploma or equivalent; some roles may prefer healthcare or research experienceRequires a bachelor's degree in health sciences or related field; certifications like CCRP are a plus
Work EnvironmentRemote or flexible settings, reviewing patient data and assessmentsClinical sites, hospitals, or research facilities managing study operations
Employer & IndustryPharmaceutical companies, research organizations, CROsHospitals, research institutions, pharmaceutical companies

In summary, Parttime Clinical Research Raters primarily focus on evaluating patient data remotely, requiring minimal certifications, while Parttime Clinical Research Coordinators handle study logistics and participant management, often needing more formal education and certifications.

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Parttime Clinical Research Rater jobs near you

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA • On-site

$53K - $58K/yr

Part-time

Re-posted 29 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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