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Study Monitor Jobs (NOW HIRING)

NCSU

Study Hall Monitor

Raleigh, NC · On-site

$18.25 - $24/hr

... Monitor check-in/check-out for all student athletes entering the facility -Facilitate and maintain a study environment conducive to learning -Assist the tutorial and academic staff on tutor/student ...

Penn State University

Study Hall Monitor

University Park, PA · On-site

$11.50 - $15.25/hr

Monitoring computer lab usage * Assisting with other assigned study hall duties * Serving as a first point of contact for emergencies outside of regular business hours This position allows for up to ...

The Pennsylvania State University

Monitoring computer lab usage * Assisting with other assigned study hall duties * Serving as a first point of contact for emergencies outside of regular business hours This position allows for up to ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete source data ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

Conduct clinical study monitoring and/or oversee CRAs to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete ...

Utah State University

Study Hall Monitor

Price, UT

$11/hr

Under the direction of the Supervisor, the Study Hall Monitor will help with: * Checking in/out student athletes * Monitoring students * Finding resources on campus * Dealing with athletes being ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

Conduct clinical study monitoring and/or oversee CRAs to ensure regulatory and protocol compliance as well as overall data accuracy in accordance with the study clinical monitoring plan * Complete ...

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Study Monitor information

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How much do study monitor jobs pay per year?

As of Aug 14, 2026, the average yearly pay for study monitor in the United States is $77,317.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,000.00 and $114,000.00 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.
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Study Monitor jobs near you
Infographic showing various Study Monitor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 13% Part Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $77,317 per year, or $37.2 per hour.

Senior Clinical Study Manager

Inspire Medical Systems Inc.

Minneapolis, MN • On-site

Full-time

Posted 10 days ago

Job description

POSITION SUMMARY 

This position is for overseeing clinical activities related to one or more clinical studies and performing/managing the daily in-house operations associated with the studies. The Clinical Study Manager must be able to work independently on multiple complex clinical studies using critical thinking skills. This position may be part of a small, cross functional team or may have direct reports. 

 

MAIN DUTIES/RESPONSIBILITIES 

  • Responsible for managing clinical studies in accordance with internal standard operating procedures and applicable regulations and guidelines 
  • Collaborate with internal and external clinical team members, consultants and/or CROs to draft clinical study protocols and other clinical study documentation 
  • Oversee clinical site selection and activation 
  • Manage study safety by tracking and reporting adverse events as required by regulatory bodies, reviewing adverse event trends, and overseeing safety committees including Clinical Events Committees and Data Safety Monitoring Boards 
  • Oversee monitoring activities related to assigned clinical studies including review and approval of monitoring plan and monitoring reports, managing monitoring schedule and ensuring corrective action related to monitoring findings 
  • Develop training plans for study training and review/approve training documentation 
  • Prepare study-related reports including annual, interim and final study reports 
  • Organize and lead study-related conference calls and Investigator meetings as needed through the study 
  • Oversee investigational device allocation, distribution and reconciliation 
  • Collaborate with data management team and/or CRO to ensure appropriate data capture, query management and to identify data analysis needs 
  • Use critical thinking skills to review and analyze scientific journal articles 
  • Assist with generation and/or review of study-related abstracts, posters, presentations, manuscripts as needed 

QUALITY SYSTEM RESPONSIBILITIES 

  • Document product and therapy related field reports within the prescribed timelines and provide any necessary documents required to complete the investigation. Provide follow-up reporting as needed. 
  • Complete training requirements and competency confirmations as required for this position within the required timeline. 
  • Comply with applicable quality system procedures/policies and make suggestions for continuous process improvement. 
  • Ensure all direct reports maintain training records that comply with applicable quality system requirements. (if applicable) 

 

QUALIFICATIONS 

Educational Requirements: 

  • Required: Bachelor's Degree required 
  • Preferred: Science Degree preferred (Biology, Chemistry, etc.) 

 

Required Experience: 

  • Previous clinical research experience (minimum 5 years) required 
  • Previous clinical study management experience preferred 
  • International clinical experience preferred 
  • Previous collaboration with physician investigators 
  • Strong knowledge of clinical research study design and study monitoring functions 
  • Understanding of GCP and 21 CFR 812 
  • Experience working with Institutional Review Boards and/or Ethics Committees 
  • Strong technical writing skills 

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