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Senior Ucsf Clinical Research 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 healthcare intelligence and clinical research organisation united by a mission to bring new medicines and ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Marietta, GA · On-site

$101K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

IQVIA

Sr. Clinical Research Associate, IQVIA

Marietta, GA · On-site

$101K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

Icon plc

Senior CRA

Atlanta, GA

Sr CRA - Oncology - GA FL - Astellas 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 ...

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Senior Ucsf Clinical Research information

See Decatur, GA salary details

$21.5K

$122.3K

$201.1K

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

As of Aug 1, 2026, the average yearly pay for senior ucsf clinical research in Decatur, GA is $122,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $153,300.00 per year, depending on experience, location, and employer.

What is the difference between Senior Ucsf Clinical Research vs Clinical Research Coordinator?

AspectSenior Ucsf Clinical ResearchClinical Research Coordinator
CredentialsBachelor's or higher, often with specialized certificationsBachelor's degree, often with certification in clinical research
Work EnvironmentAcademic medical centers, research institutionsHospitals, clinics, research sites
ResponsibilitiesOverseeing study protocols, managing teams, ensuring complianceParticipant recruitment, data collection, study coordination
Experience LevelMid to senior-level with extensive research experienceEntry to mid-level, focused on coordination tasks

The main difference is that Senior Ucsf Clinical Research roles involve overseeing research projects and managing teams, while Clinical Research Coordinators focus on day-to-day study operations and participant management. Senior roles require more experience and often additional certifications, whereas coordinators handle the operational aspects of clinical trials.

What are popular job titles related to Senior Ucsf Clinical Research jobs in Decatur, GA? For Senior Ucsf Clinical Research jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Senior Ucsf Clinical Research jobs in Decatur, GA look for? The top searched job categories for Senior Ucsf Clinical Research jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Senior Ucsf Clinical Research jobs? Cities near Decatur, GA with the most Senior Ucsf Clinical Research job openings:
Senior Ucsf Clinical Research jobs near you

Senior Clinical Research Associate

Icon plc

Atlanta, GA

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 4 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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