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Entry Level Clinical Research Associate 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

$101.60K - $169.30K/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

$101.60K - $169.30K/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:

Alcanza

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

A Medical Assistant diploma, LPN/LVN, EMT credential OR Associate's degree AND a minimum of 1 year of clinical research or clinical experience, OR an equivalent combination of education and ...

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Entry Level Clinical Research Associate information

What is an Entry Level Clinical Research Associate job?

An Entry Level Clinical Research Associate (CRA) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements, ethical guidelines, and study protocols. They assist in site selection, data collection, and verifying that study procedures are properly followed. Entry-level CRAs typically work under the supervision of senior CRAs and may travel to different clinical sites. Strong attention to detail, knowledge of Good Clinical Practice (GCP) guidelines, and organizational skills are essential. This role is a starting point for a career in clinical research, with opportunities for growth into senior CRA or project management positions.

What are the key skills and qualifications needed to thrive in the Entry Level Clinical Research Associate position, and why are they important?

To thrive as an Entry Level Clinical Research Associate, you typically need a bachelor's degree in life sciences or a related field, a solid understanding of clinical trial protocols, and attention to detail. Familiarity with Good Clinical Practice (GCP) guidelines, electronic data capture (EDC) systems, and regulatory documentation is often required. Strong communication, organization, and problem-solving abilities help you effectively collaborate with study sites and team members. These skills are critical to ensure the accuracy, compliance, and successful progression of clinical studies.

What are the typical daily responsibilities of an Entry Level Clinical Research Associate?

As an Entry Level Clinical Research Associate, your day-to-day work generally involves assisting with monitoring clinical trial sites, reviewing study documentation, and ensuring adherence to protocol and regulatory requirements. You may support more senior team members in conducting on-site or remote visits, tracking patient recruitment, and managing data collection. Additionally, you’ll communicate regularly with site staff and other stakeholders to resolve issues and ensure data quality. This hands-on experience is essential for building expertise in clinical research processes and advancing toward more senior CRA roles.
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Entry Level Clinical Research Associate jobs near you
Senior Clinical Research Associate

Senior Clinical Research Associate

Icon plc

Atlanta, GA

Full-time

Medical, Dental, Vision, Life, Retirement

Posted yesterday

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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