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Associate Clinical Scientist information

See Decatur, GA salary details

$27

$53

$79

How much do associate clinical scientist jobs pay per hour?

As of May 31, 2026, the average hourly pay for associate clinical scientist in Decatur, GA is $53.45, according to ZipRecruiter salary data. Most workers in this role earn between $39.18 and $66.63 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Associate Clinical Scientist, and why are they important?

To thrive as an Associate Clinical Scientist, you need a solid foundation in biological sciences, analytical skills, and usually at least a bachelor's degree in a relevant field. Familiarity with laboratory information management systems (LIMS), statistical analysis tools, and regulatory standards such as GLP or GCP is typically expected. Strong attention to detail, teamwork, and effective written and verbal communication set exceptional candidates apart. These competencies ensure accurate data collection, regulatory compliance, and effective collaboration in clinical research environments.

How does an Associate Clinical Scientist typically collaborate with cross-functional teams during a clinical trial?

As an Associate Clinical Scientist, you will regularly work with multidisciplinary teams including clinical operations, data management, regulatory affairs, and biostatistics. Your role often involves supporting the design and execution of clinical studies, ensuring protocols are followed, and communicating scientific findings. Effective collaboration is key, as you may participate in team meetings, contribute to study documentation, and help resolve study-related issues. This collaborative environment fosters learning from experienced colleagues and provides a well-rounded view of the clinical development process.

What are Associate Clinical Scientists?

Associate Clinical Scientists are professionals who support the design, implementation, and monitoring of clinical trials and research studies in healthcare and pharmaceutical settings. They work closely with clinical teams to ensure that studies comply with regulatory requirements and scientific standards. Their responsibilities may include collecting and analyzing data, preparing reports, and assisting with protocol development. Typically, they have a background in life sciences and are involved in advancing medical research and improving patient care.

What is the difference between Associate Clinical Scientist vs Clinical Research Associate?

AspectAssociate Clinical ScientistClinical Research Associate
Required CredentialsBachelor's or Master's in life sciences, relevant certificationsBachelor's in life sciences, often with certifications in clinical trials
Work EnvironmentResearch labs, pharmaceutical companies, biotech firmsClinical trial sites, hospitals, research organizations
Employer & Industry UsagePharmaceutical, biotech, medical device companiesContract research organizations, pharmaceutical companies
Common Search & ComparisonYesYes

The Associate Clinical Scientist and Clinical Research Associate roles share similarities in industry and required credentials, but differ mainly in work environment and focus. The Associate Clinical Scientist typically works in research labs or biotech firms focusing on data analysis and scientific development, while the Clinical Research Associate is more involved in monitoring clinical trials at trial sites. Both roles are essential in the clinical research process, with overlapping skills and industry usage.

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

Sr. Clinical Research Associate, IQVIA

IQVIA

Marietta, GA

$101.60K - $169.30K/yr

Full-time

Posted 12 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

53rd of 203 rated it services

Job description

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:

Job Overview:

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Key Responsibilities:

Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.

Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.

Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.

Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.

Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Collaborate and liaise with study team members for project execution support as appropriate. Responsibilities Essential Functions If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.

If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications:

Bachelor's Degree in scientific discipline or health care preferred.

Requires at least 2 years of year of on-site monitoring experience.

Equivalent combination of education, training and experience may be accepted in lieu of degree.

Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.

Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Good therapeutic and protocol knowledge as provided in company training.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $101,600.00 - $169,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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