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Research Data Associate Jobs in Pennsylvania (NOW HIRING)

System One

Clinical Research Coordinator

West Chester, PA · On-site

$26 - $30/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Collect, record, and maintain accurate clinical research data and source documentation in ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

The Pennsylvania State University

Collect, prepare, and analyze research data; experience in collecting and analyzing HPLC and proteomics and mass spectrometry data is required. * Design and execute mass spectrometry imaging ...

Kelly Services

Clinical Research Coordinator

West Chester, PA

$28 - $30/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Collect, record, and maintain accurate clinical research data and source documentation in ... High school diploma or equivalent required; an associate's degree or higher in a health-related ...

Actalent

Clinical Research Nurse

Philadelphia, PA · Hybrid

$35 - $46/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Collect and document clinical research data. * Conduct chart reviews and support adverse event ... Nursing Diploma or Associate Degree required; BSN preferred. * Minimum 2 years of healthcare ...

Actalent

Clinical Research Nurse

Philadelphia, PA · Hybrid

$35 - $46/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Collect and document clinical research data. * Conduct chart reviews and support adverse event ... Nursing Diploma or Associate Degree required; BSN preferred. * Minimum 2 years of healthcare ...

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Showing results 21-40

All JobsResearch Data Associate JobsResearch Data Associate Jobs in Pennsylvania

Research Data Associate information

See Pennsylvania salary details

$16

$32

$46

How much do research data associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for research data associate in Pennsylvania is $32.62, according to ZipRecruiter salary data. Most workers in this role earn between $26.25 and $37.12 per hour, depending on experience, location, and employer.

What are some common challenges research data associates face when managing large datasets, and how can they be addressed?

Research Data Associates often encounter challenges such as ensuring data quality, maintaining accurate documentation, and handling missing or inconsistent data within large datasets. To address these, they typically implement rigorous data cleaning protocols, work closely with research teams to standardize data collection processes, and use specialized software for data validation. Collaborating with statisticians and IT staff is also essential to resolve technical issues and maintain data integrity throughout the project lifecycle.

How much is a research data associate paid?

Research Data Associates typically earn between $40,000 and $60,000 annually, depending on experience, education, and location. Entry-level positions may start lower, while those with specialized skills or certifications can earn higher salaries. Compensation often includes benefits such as health insurance and paid time off.

What are the key skills and qualifications needed to thrive as a research data associate?

To thrive as a Research Data Associate, you generally need strong quantitative analysis skills, attention to detail, and a relevant bachelor's degree in fields like statistics, data science, or a related discipline. Familiarity with data management tools such as SQL, SPSS, R, or Python, as well as experience with data collection and cleaning processes, is typically required. Effective communication, problem-solving, and collaboration skills help Research Data Associates work efficiently within research teams and convey findings clearly. These competencies ensure accurate data handling, meaningful analysis, and the reliability of research outcomes.

What is a research data associate?

Research Data Associates are professionals who support research projects by managing, analyzing, and interpreting data. They are responsible for collecting data, ensuring its quality, maintaining databases, and preparing reports or summaries for research teams. Their work is essential in academic, medical, or industrial research settings, where accurate and reliable data is crucial for decision-making and publication. Research Data Associates often collaborate with researchers, statisticians, and IT staff to ensure data integrity and security.

What does a research data associate do?

A research data associate is responsible for collecting, organizing, and analyzing data for research projects. They often use statistical software and data management tools to ensure data accuracy and integrity, supporting researchers in drawing valid conclusions. The role typically requires attention to detail and familiarity with data handling procedures.

What are the most commonly searched types of Research Data jobs in Pennsylvania?

The most popular types of Research Data jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Research Data Associate jobs?

Cities in Pennsylvania with the most Research Data Associate job openings:

Research Data Associate jobs near you
Infographic showing various Research Data Associate job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 17% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $67,848 per year, or $32.6 per hour.

Clinical Research Coordinator

System One

West Chester, PA • On-site

$26 - $30/hr

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 16 days ago

Job description

Job Title: Clinical Research Coordinator Location: West Chester, Pennsylvania Type: Contract (with opportunity for conversion to permanent) Compensation: $26.00 - $30.00/hr (dependent on experience) Work Model: Onsite Hours: 40.0

Responsibilities • Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. • Conduct screening visits to collect medical history & other information from study participants. • Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines. • Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams. • Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards. • Communicate with study participants to provide education, answer questions, and support adherence to study requirements. • Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team. • Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines. • Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified.) • Scan, upload, file, and maintain organized study records and documentation. • Apply critical thinking skills to support efficient study operations and problem resolution. • Perform other duties as assigned.

Requirements • High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred. • Basic knowledge of clinical research strongly preferred. • Medical terminology & patient care experience required. • Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities. • Ability to communicate clearly and professionally with diverse populations. • Ability to work collaboratively in a fast-paced, team-oriented environment. • Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred. • Experience with participant screening and the informed consent process strongly preferred. • Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred. • Medical Assistant (MA) certification preferred. • Current CPR/BLS certification preferred. • Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M- #LI- Ref: #568-Clinical