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Clinical Research Associate Monitor Jobs in Decatur, GA

ICON

Senior Clinical Research Associate

Atlanta, GA · On-site +1

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions ICON is a global ... The ideal candidate will have cardiovascular medical device monitoring experience- however ...

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How much do clinical research associate monitor jobs pay per hour?

As of May 30, 2026, the average hourly pay for clinical research associate monitor in Decatur, GA is $40.15, according to ZipRecruiter salary data. Most workers in this role earn between $28.17 and $51.39 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate Monitor, and why are they important?

To thrive as a Clinical Research Associate Monitor, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and FDA regulations), and often 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 typically required. Excellent attention to detail, strong organizational skills, and effective communication are crucial soft skills for liaising with site staff and ensuring protocol compliance. These competencies ensure that clinical trials are conducted ethically, accurately, and in adherence to regulatory standards, safeguarding data integrity and patient safety.

What are some common challenges Clinical Research Associate Monitors face when overseeing multiple clinical trial sites?

Clinical Research Associate Monitors often manage several clinical trial sites simultaneously, which can present challenges such as coordinating schedules, ensuring consistent protocol adherence, and managing documentation across diverse teams. Effective communication and strong organizational skills are crucial to address site-specific issues promptly and maintain regulatory compliance. Additionally, frequent travel and adapting to varying site cultures are common aspects of the role, and building strong relationships with site staff can greatly enhance trial success.

What is a Clinical Research Associate Monitor?

A Clinical Research Associate Monitor is a professional responsible for overseeing clinical trials to ensure they are conducted in accordance with regulatory requirements, Good Clinical Practice (GCP) guidelines, and study protocols. They monitor trial sites, review documentation, verify data accuracy, and ensure the safety and rights of study participants. Their work is crucial in maintaining the integrity of clinical research and facilitating the development of new medical treatments.
What job categories do people searching Clinical Research Associate Monitor jobs in Decatur, GA look for? The top searched job categories for Clinical Research Associate Monitor jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Research Associate Monitor jobs? Cities near Decatur, GA with the most Clinical Research Associate Monitor job openings:
Clinical Research Associate Monitor jobs near you
Senior Clinical Research Associate

Senior Clinical Research Associate

Icon plc

Atlanta, GA

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago

Job description

Senior Clinical Research Associate - Cardio (Smartpulse A-fib) - All Regions

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


To support 1study in the cardiovascular/electrophysiology medical device space. Indication is A-fib.

  • The ideal candidate will have cardiovascular medical device monitoring experience- however, cardiovascular/electrophysiology pharma monitoring experience will be considered.

3 years of monitoring experience required.

A bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.

Candidates must have/ be:

  • In-depth knowledge of FDA regulations and ICH/GCP guidelines.

  • Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.

  • Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.

  • Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.

  • Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.

  • Ability to work independently and manage multiple priorities in a dynamic environment.

  • A well-executed plan for communication with the study teams and sites.

  • Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports.

  • Located in the US near a major airport. Ability to cover up to 65% regional travel.


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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