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Senior Clinical Research Regulatory 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 ... In-depth knowledge of FDA regulations and ICH/GCP guidelines. * Strong problem-solving skills to ...

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Senior Clinical Research Regulatory information

See Decatur, GA salary details

$35.1K

$92.1K

$140.1K

How much do senior clinical research regulatory jobs pay per year?

As of Aug 27, 2026, the average yearly pay for senior clinical research regulatory in Decatur, GA is $92,082.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $125,000.00 per year, depending on experience, location, and employer.

What does a senior clinical research regulatory do?

A Senior Clinical Research Regulatory professional is responsible for ensuring that clinical research studies comply with regulatory requirements and ethical standards. They oversee the preparation and submission of regulatory documents to agencies such as the FDA or IRB, monitor compliance throughout the study, and provide guidance to research teams on regulatory matters. Their expertise helps safeguard the rights and safety of study participants while enabling the successful approval and conduct of clinical trials.

What are some common challenges senior clinical research regulatory face when coordinating multi-site studies?

Senior Clinical Research Regulatory professionals often encounter challenges such as ensuring consistent regulatory compliance across multiple sites, managing varying timelines for local IRB approvals, and aligning documentation to meet both sponsor and regulatory authority requirements. Effective communication and meticulous organization are key to overcoming these obstacles, as the role frequently involves coordinating with investigators, site staff, and regulatory agencies. Staying updated on changing regulations and providing guidance to teams ensures successful study start-up and ongoing compliance throughout the trial.

What are the key skills and qualifications needed to thrive as a senior clinical research regulatory, and why are they important?

To excel as a Senior Clinical Research Regulatory professional, you need in-depth knowledge of clinical research regulations, compliance standards, and experience with regulatory submissions, typically supported by a bachelor’s or advanced degree in life sciences or a related field. Familiarity with regulatory systems such as FDA, EMA, ICH-GCP guidelines, and electronic submission platforms is essential, and certifications like RAC are highly valued. Exceptional attention to detail, strong organizational skills, and effective communication are critical soft skills for managing complex documentation and cross-functional collaboration. These competencies ensure that clinical trials meet legal requirements, maintain participant safety, and progress efficiently through regulatory review.

What is the difference between Senior Clinical Research Regulatory vs Clinical Research Associate?

AspectSenior Clinical Research RegulatoryClinical Research Associate
CredentialsTypically requires a Bachelor's or Master's in life sciences, with regulatory certifications preferredBachelor's degree in life sciences or related field; certifications are a plus
Work EnvironmentFocuses on regulatory compliance, document review, and submissions within clinical trial teamsMonitors clinical sites, ensures protocol adherence, and collects data during trials
Employer & Industry UsageUsed in pharmaceutical, biotech, and CRO companies for regulatory tasksCommonly employed in clinical trial sites, CROs, and pharmaceutical companies

The main difference is that Senior Clinical Research Regulatory professionals handle regulatory submissions and compliance, while Clinical Research Associates focus on site monitoring and data collection. Both roles are essential in clinical trials but serve different functions within the research process.

What are the most commonly searched types of Clinical Research Regulatory jobs in Decatur, GA?

The most popular types of Clinical Research Regulatory jobs in Decatur, GA are:

Senior Clinical Research Regulatory jobs near you

Senior Clinical Research Associate

Atlanta, GA

Icon plc
See more jobs at Icon plcexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 16 hours 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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