ZipRecruiter

Log In

1

Clinical Affairs Associate Jobs in Georgia (NOW HIRING)

Agilent

Clinical Affairs Scientist

Turin, GA · On-site +1

$105K - $197K/yr

The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance ...

Danaher

Principal Clinical Scientist

Atlanta, GA · On-site +1

Our associates are involved in every stage of diagnostics, from ideation to development and ... Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to ...

next page

Showing results 1-20

All JobsClinical Affairs Associate JobsClinical Affairs Associate Jobs in Georgia

Clinical Affairs Associate information

See Georgia salary details

$10

$26

$46

How much do clinical affairs associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical affairs associate in Georgia is $26.63, according to ZipRecruiter salary data. Most workers in this role earn between $17.88 and $35.10 per hour, depending on experience, location, and employer.

What is a clinical affairs associate?

A Clinical Affairs Associate is a professional who supports clinical research and regulatory activities within healthcare or medical device organizations. Their primary responsibilities include assisting with the planning, execution, and monitoring of clinical trials, ensuring compliance with regulatory requirements, and helping prepare documentation for submissions to regulatory bodies. They often coordinate between internal teams, external vendors, and regulatory agencies to ensure the smooth progress of clinical studies. This role is crucial for ensuring that new medical products are safe, effective, and meet all necessary regulatory standards before reaching the market.

What are the key skills and qualifications needed to thrive as a clinical affairs associate, and why are they important?

To thrive as a Clinical Affairs Associate, you need a solid understanding of clinical research processes, regulatory requirements, and data management, typically supported by a degree in life sciences or a related field. Familiarity with tools like electronic data capture (EDC) systems, clinical trial management systems (CTMS), and knowledge of GCP guidelines is essential. Strong attention to detail, organizational skills, and effective communication are standout soft skills in this role. These competencies ensure accurate documentation, regulatory compliance, and smooth coordination of clinical trial activities.

What are some typical challenges faced by clinical affairs associates when managing clinical trial documentation?

Clinical Affairs Associates often encounter challenges in ensuring all clinical trial documentation is accurate, up-to-date, and compliant with regulatory standards. Managing multiple studies simultaneously can lead to tight deadlines and the need for meticulous attention to detail. Effective communication with cross-functional teams, such as clinical operations, regulatory affairs, and data management, is essential to resolve discrepancies and maintain data integrity. Staying organized and keeping abreast of evolving regulatory requirements are key to overcoming these challenges.

What are the most commonly searched types of Clinical Affairs jobs in Georgia?

The most popular types of Clinical Affairs jobs in Georgia are:

What are popular job titles related to Clinical Affairs Associate jobs in Georgia?

For Clinical Affairs Associate jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Clinical Affairs Associate jobs in Georgia look for?

The top searched job categories for Clinical Affairs Associate jobs in Georgia are:

What cities in Georgia are hiring for Clinical Affairs Associate jobs?

Cities in Georgia with the most Clinical Affairs Associate job openings:

Clinical Affairs Associate jobs near you
Infographic showing various Clinical Affairs Associate job openings in Georgia as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $55,395 per year, or $26.6 per hour.

Clinical Affairs Scientist

Agilent

Turin, GA • On-site, Remote

$105K - $197K/yr

Full-time

Posted 15 days ago

Key responsibilities

  • Support clinical trial study designs and execution, including authoring study protocols and reports.

  • Collaborate with cross-functional teams and external partners to generate clinical evidence and ensure compliance with regulatory requirements.

  • Provide scientific oversight and contribute to the development of clinical and scientific documentation, including manuscripts, abstracts, and presentations.

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Job Description

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer(OCMO) Global Clinical Affairs team. The CAS' main responsibilities will be to support clinical evidence generation, in conjunction with cross-functional teams as part of the co-development process of companion diagnostics in the field of oncology. This position will support clinical trial study designs and execution, regulatory applications, and scientific marketing deliverables. The ideal candidate will have a strong background in clinical science/research and experience working in pharmaceutical, biomarker, and/or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. This position reports to the Manager of Clinical Affairs Sciences and has no direct reports.
Responsibilities include but are not limited to:

  • Provide thought leadership on key relevant clinical topics to support strategy development and execution.

  • Generation of content to support external validation studies including study design and authoring of study protocols and reports. May also contribute to cutoff/cutpoint determination studies, method comparison, bridging, and analytical concordance studies.

  • Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms.

  • Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials.

  • Ensure scientific validity of reported results including statistical analysis, tabulation, and presentation of data.

  • Collaborate with regulatory and development teams during the submission process including authoring of clinical performance information and other documentation such as Instructions for Use (IFU).

  • Provide clinical and scientific oversight of local marketing and commercial materials.

  • Ensure effective, efficient and compliant Clinical Affairs processes including preparing, revising, and maintaining standard operating procedures for the conduct of clinical studies.

  • Serve as the clinical science subject matter expert in cross-functional internal meetings as well as meetings with pharmaceutical partners and regulatory bodies.

  • Author manuscripts, abstracts, whitepapers and prepare oral/poster presentations.

  • Support audits and inspections as a clinical subject matter expert.

Qualifications

  • Master's degree or advanced degree (e.g., Ph.D., Pharm. D., M.D.) in pharmaceutical, medical or relevant biomedical science fields. Advanced Degree preferred.

  • 4+ years of experience in IVD product development, clinical research, medical writing, and/or clinical science in the medical device and/or pharmaceutical industry.

  • Familiarity with clinical trial design, conduct, and oversight including biostatistics, and Good Clinical Practice preferred.

  • Ability to interpret regulatory standards, guidance, and laws.

  • Strong scientific, medical writing, and presentation skills

  • Exceptional ability to manage multiple projects in a fast-paced environment with changing priorities.

  • Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments.

  • Experience working with external partners and/or regulatory bodies including the FDA.

  • Knowledge in oncology, immunology, and/or pathology preferred.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 27, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $105,280.00 - $197,400.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: Medical/Clinical

What Agilent Technologies employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply