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Clinical Data Monitor Jobs (NOW HIRING)

Agilent

The Clinical Data Manager will plan and oversee all data management activities across assigned ... data monitoring, andmaintaindata in reporting platforms. The role will collaborate with cross ...

Ambu

Clinical Data Manager

Columbia, MD · On-site

Clinical Data Manager City: Columbia, MD Country/Region: United States State: Business Area ... Monitor enrollment, site performance, study milestones, and overall study progress while ...

Ocugen Inc

Senior Clinical Data Manager

Malvern, PA · On-site

... monitoring, and validation for clinical development programs and marketed products. In addition to technical responsibilities, the Senior Clinical Data Manager will provide leadership to junior data ...

OCUGEN OPCO INC

Senior Clinical Data Manager

Malvern, PA · On-site

... monitoring, and validation for clinical development programs and marketed products. In addition to technical responsibilities, the Senior Clinical Data Manager will provide leadership to junior data ...

Abbott

MN · On-site

$45 - $47/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The ... Conduct Central Monitoring activities, as described in Central Monitoring Plan. Direct all data ...

AccuScan Sciences

Clinical Data Manager

Milpitas, CA · On-site

Position Summary The Clinical Data Manager (CDM) is responsible for the end-to-end management ... Run and monitor pipelines for data reprocessing and corrections * Interface with bioinformatics ...

AccuScan Sciences

Clinical Data Manager

Milpitas, CA · On-site

... and monitor pipelines for data reprocessing and corrections Interface with bioinformatics pipelines via command line and scripting Troubleshoot data issues end-to-end from raw data through final ...

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Clinical Data Monitor information

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How much do clinical data monitor jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical data monitor in the United States is $38.49, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $51.20 per hour, depending on experience, location, and employer.

What is a clinical data monitor?

A Clinical Data Monitor is a professional responsible for overseeing the accuracy, integrity, and security of data collected during clinical trials. They ensure that clinical trial data is collected, entered, and reported according to regulatory standards and study protocols. Their work helps maintain the quality of data used to assess the safety and effectiveness of new drugs or medical devices. Clinical Data Monitors often collaborate with clinical research coordinators, data managers, and regulatory authorities to ensure compliance and resolve any data discrepancies.

How does a clinical data monitor typically interact with other teams during a clinical trial?

Clinical Data Monitors work closely with various teams such as clinical research associates (CRAs), data management, and biostatistics. They are responsible for ensuring the accuracy and integrity of clinical trial data by regularly reviewing case report forms and addressing discrepancies with site staff and data managers. Effective communication and collaboration are crucial, as Clinical Data Monitors often need to provide feedback, clarify data inconsistencies, and ensure all regulatory and protocol requirements are met throughout the trial.

How to become a clinical data monitor?

To become a clinical data monitor, typically a bachelor's degree in health sciences, life sciences, or a related field is required. Relevant skills include knowledge of clinical trial processes, data management, and familiarity with electronic data capture systems; obtaining certifications like the Society of Clinical Data Management (SCDM) certification can enhance prospects. Gaining experience through internships or entry-level roles in clinical research is also beneficial.

What are the key skills and qualifications needed to thrive as a clinical data monitor, and why are they important?

To thrive as a Clinical Data Monitor, you need a solid understanding of clinical research processes, data management, and regulatory compliance, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Attention to detail, analytical thinking, and strong communication skills set outstanding professionals apart in this role. These skills are crucial to ensure the accuracy, integrity, and regulatory compliance of clinical trial data, which supports successful drug development and patient safety.

What is the difference between Clinical Data Monitor vs Clinical Data Coordinator?

AspectClinical Data MonitorClinical Data Coordinator
CredentialsTypically requires a degree in life sciences or healthcare, often with certifications like CDMP or CDISCUsually holds a degree in health sciences or related field, with similar certifications
Work EnvironmentWorks primarily on data review, monitoring clinical trial sites, and ensuring data qualityHandles data entry, management, and coordination between sites and sponsors
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch organizations, hospitals, clinical trial sites

The Clinical Data Monitor focuses on reviewing and verifying clinical trial data to ensure accuracy and compliance, often working directly with sites. The Clinical Data Coordinator manages data entry and organization, supporting the data collection process. Both roles require similar educational backgrounds and certifications but differ in daily responsibilities and focus areas.

More about Clinical Data Monitor jobs
What states have the most Clinical Data Monitor jobs? States with the most job openings for Clinical Data Monitor jobs include:
What job categories do people searching Clinical Data Monitor jobs look for? The top searched job categories for Clinical Data Monitor jobs are:
Clinical Data Monitor jobs near you
Infographic showing various Clinical Data Monitor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $80,060 per year, or $38.5 per hour.

Clinical Data Monitor (Part-time) / Madison, WI (On-site)

Fortrea

Madison, WI • On-site

Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

25th of 73 rated research

Job description

As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US.
We are currently seeking a Clinical Data Monitor, to interact directly with our healthy volunteer participants while learning to read clinical research protocols and enjoy working in a fast-paced team-oriented environment. Each day is different, you will be exposed to a wide variety of Therapeutic Indications and study types (ascending dose, first-in-human, food effect, drug to drug interactions, etc.)
This is a part-time, office/clinic-based job in Madison, WI .
If you join us, you will work with some of the world's leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability and pharmacokinetics of a new drug.
Many are drawn to this profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to have a close face-to-face relationship with participants, and as you continue to practice your clinical skills and knowledge, you'll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you worked with gets approved, you know you'll touch many patient's lives around the world.
WHAT YOU WILL DO:
You will utilize your skills, knowledge, and clinical judgement for all aspects of data capture, review and quality for Phase I studies. The Clinical Data Monitor I is someone who ensures that all data and information is produced on time, in accordance with defined quality standards and meets the requirements of the business and our customers.
Other key responsibilities:
  • Data Planning - responsible for all data aspects of studies including review of draft
    protocols, attending Clinic Start Up Meetings, supporting the workbook (CRF) design process, training plans for non-standard study data capture and attend Biometrics start up meetings as required.
  • Ensure that the data entry and QC of dose escalation data is completed within the
    required timelines.
  • Complete daily ongoing QC of all study data across Clinical Operations including daily
    shop floor QC.
  • Query Resolution - ensure all database queries; sponsors written data queries, CRA
    monitoring queries and internal QA audit findings are resolved within the agreed timelines.
  • Responsible for ensuring the weekly Data Entry Schedule is updated and accurately reflects study workload.
  • Study Close Down - Ensure completed CRF's are signed by the Principal or Associate
    Investigator and that all CRF's and source data is archived on completion of the study.
  • And perform other job-related duties and or tasks as assigned.

YOU NEED TO BRING...
  • B.Sc. degree in Life Science / Pharmacy or equivalent related discipline is preferred
  • Must be able to demonstrate working knowledge of Microsoft Office.
  • Language Skills: English Required (Speaking, Writing, and Reading)
  • In lieu of education relevant job experience will be considered.
  • Typically looking for 1-2 years of data handling experience. Experience can be from a clinical or non-clinical background. For example, financial data handling background.

The important thing for us is you are comfortable working in an environment that is:
  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.

What do you get?
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO)
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)

Physical Requirements:
  • Ability to work in an upright and /or stationary position for 6-8 hours per day.
  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment.
  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
  • Regular and consistent attendance.
  • Varied hours may be required.

Learn more about our EEO & Accommodations request here.

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