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Study Monitor Jobs in Pennsylvania (NOW HIRING)

UPMC Passavant

Full-Time Monitor Technician

Pittsburgh, PA

$19 - $24.25/hr

Ability to push ECGs machines on carts with wheels in order to perform studies in various areas throughout the hospital. * Provides visual surveillance of numerous cardiac monitors simultaneously ...

Icon plc

Integrated Study Timeline Manager

Blue Bell, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Monitor project progress and identify potential delays or roadblocks * Work with cross functional ... Review of study related material and protocol to drive discussion related to study timelines.

ICON

Integrated Study Timeline Manager

Blue Bell, PA · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Monitor project progress and identify potential delays or roadblocks * Work with cross functional ... Review of study related material and protocol to drive discussion related to study timelines.

ICON

Integrated Study Timeline Manager

Center Square, PA · On-site

$110 - $140/hr

  • Medical

  • Life

  • Retirement

  • PTO

Monitor project progress and identify potential delays or roadblocks * Work with cross functional ... Review of study related material and protocol to drive discussion related to study timelines.

410 ICR United States USA

Medical Monitor

United, PA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

We are looking for a board certified professional with experience in monitoring Obesity/GLP-1 studies. What You Will Do: You will lead medical affairs delivery across your portfolio, setting ...

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Showing results 21-40

All JobsStudy Monitor JobsStudy Monitor Jobs in Pennsylvania

Study Monitor information

See Pennsylvania salary details

$15.3K

$69.6K

$124.2K

How much do study monitor jobs pay per year?

As of Aug 14, 2026, the average yearly pay for study monitor in Pennsylvania is $69,567.00, according to ZipRecruiter salary data. Most workers in this role earn between $39,589.00 and $102,572.00 per year, depending on experience, location, and employer.

What does a study monitor do?

A study monitor oversees clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. They review data for accuracy, verify patient safety, and ensure proper documentation, often using electronic data capture systems. Monitoring typically involves site visits, communication with staff, and reporting findings to sponsors or regulatory bodies.

What are the key skills and qualifications needed to thrive as a study monitor?

To thrive as a Study Monitor, you need a strong understanding of clinical trial protocols, regulatory guidelines (such as GCP), and data integrity principles, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are commonly expected. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills. These competencies ensure high-quality study oversight, compliance with regulations, and smooth collaboration among clinical research teams.

What are some common challenges study monitors face during clinical trials?

Study Monitors often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing discrepancies in data, and navigating tight timelines for site visits and reporting. They must adapt quickly to evolving regulatory requirements and effectively communicate any issues or deviations to investigators and sponsors. Being proactive in identifying potential risks and fostering strong relationships with site staff can help minimize these challenges. As a result, successful Study Monitors need to be resourceful, detail-oriented, and skilled at balancing regulatory compliance with practical problem-solving in dynamic trial environments.

What is a study monitor?

A Study Monitor, also known as a Clinical Research Associate (CRA), is responsible for overseeing clinical trials to ensure they comply with regulatory guidelines, study protocols, and ethical standards. They monitor site activities, review data accuracy, and ensure participant safety. Study Monitors work closely with investigators, site staff, and sponsors to ensure the integrity of trial results and adherence to Good Clinical Practice (GCP) guidelines.

How do you become a study monitor?

To become a study monitor, candidates typically need to be students with good academic standing and demonstrate responsibility. Schools or organizations may require an application, a teacher or supervisor recommendation, and sometimes an interview. Relevant skills include organization, communication, and the ability to supervise peers in a classroom or study environment.

What are popular job titles related to Study Monitor jobs in Pennsylvania?

For Study Monitor jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Study Monitor jobs in Pennsylvania look for?

The top searched job categories for Study Monitor jobs in Pennsylvania are:

Study Monitor jobs near you
Infographic showing various Study Monitor job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, 1% Temporary, 3% Contract, and 2% Nights. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $69,567 per year, or $33.4 per hour.

CLINICAL RESEARCH MONITOR

The Fox Chase Cancer Center Foundation

Philadelphia, PA • On-site, Remote

Full-time

Posted 17 days ago

Job description

The OCR Clinical Research Monitor, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level.
Monitors all extramural research program investigator initiated studies being conducted at FCCC and other academic institutions. Ensures protocol compliance at the clinical research sites. Other applicable certification may be considered in lieu of those listed below (i.e

Regulatory Affairs).
Education
Bachelor's Degree Science or other health care discipline Required or
Combination of relevant education and experience may be considered in lieu of degree Required
Experience
2 years experience in clinical research monitoring/auditing Preferred
2 years experience in oncology Preferred
2 years experience working in clinical research Preferred
Licenses
Cert Clin Research Coordinator Preferred or
Cert Clin Research Associate Preferred
Cert Clin Research Prof Preferred

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