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Medical Biotech Jobs in Georgia (NOW HIRING)

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA

CRA 1, IQVIA Biotech

Marietta, GA · On-site

$71K - $145K/yr

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have ... innovative medical treatments to help improve patient outcomes and population health worldwide.

MMS

Senior Medical Writer (Remote)

Atlanta, GA · On-site

About MMS MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, and medical device industries with a proven, scientific approach to complex trial data and regulatory ...

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Medical Biotech information

See Georgia salary details

$30.8K

$139.1K

$284.6K

How much do medical biotech jobs pay per year?

As of Aug 15, 2026, the average yearly pay for medical biotech in Georgia is $139,096.00, according to ZipRecruiter salary data. Most workers in this role earn between $54,000.00 and $226,700.00 per year, depending on experience, location, and employer.

What can I do with a medical biotechnology degree?

A medical biotechnology degree prepares individuals for roles in research and development, clinical laboratories, and pharmaceutical companies. Graduates can work as research scientists, laboratory technicians, quality assurance specialists, or regulatory affairs professionals, often utilizing skills in molecular biology, cell culture, and data analysis. Certification and familiarity with laboratory tools and protocols enhance employment opportunities in healthcare and biotech industries.

What are the key skills and qualifications needed to thrive as a medical biotech professional?

To thrive as a Medical Biotech professional, you need a solid background in molecular biology, genetics, and laboratory techniques, often supported by a degree in biotechnology or a related field. Familiarity with lab equipment, PCR, data analysis software, and sometimes certifications like GLP (Good Laboratory Practice) are typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help professionals excel in research and teamwork. These skills and qualities are crucial for ensuring scientific accuracy, regulatory compliance, and successful innovation in medical biotechnology.

What is a medical biotech professional?

Medical biotech professionals are scientists and technicians who use biological processes and technologies to develop products and solutions that improve human health. They work in areas such as developing new drugs, gene therapies, diagnostic tools, and vaccines. These professionals may be involved in laboratory research, clinical trials, regulatory affairs, or manufacturing. Their work often bridges the gap between scientific discovery and practical medical applications, contributing to advances in healthcare and treatment options.

Is medical biotechnology a good career?

Medical biotechnology is a growing field that involves developing medical products, therapies, and diagnostics using biological systems and organisms. It offers opportunities in research, development, and manufacturing, often requiring strong scientific skills and knowledge of laboratory techniques. The career can be rewarding for those interested in advancing healthcare and biotechnology innovations.

What are some common challenges faced by medical biotech professionals, and how can they be addressed?

Professionals in medical biotech often encounter challenges such as keeping pace with rapidly evolving technologies, navigating complex regulatory requirements, and managing cross-disciplinary collaboration. Staying current with scientific advancements requires continuous learning and adaptability. Regulatory compliance can be addressed through regular training and close coordination with quality assurance teams. Additionally, success in this field often depends on strong communication skills to effectively collaborate with research scientists, clinicians, and regulatory specialists.

What does a medical biotechnologist do?

A medical biotechnologist researches and develops technologies to improve healthcare, such as creating diagnostic tools, developing new treatments, and studying disease mechanisms. They often work in laboratories, using techniques like molecular biology and cell culture, and may require specialized training or certifications. Their work supports advancements in medical diagnostics, therapeutics, and personalized medicine.

What is the difference between Medical Biotech vs Clinical Research Associate?

AspectMedical BiotechClinical Research Associate
Required CredentialsBiotech degree, lab skills, sometimes advanced degreesLife sciences degree, clinical trial knowledge, certifications
Work EnvironmentLaboratories, biotech companies, research facilitiesClinical sites, hospitals, research organizations
Employer & Industry UsageBiotech firms, pharmaceutical companies, research institutionsPharmaceutical companies, CROs, hospitals

Medical Biotech professionals focus on developing and testing biotechnological products, often working in labs and research settings. Clinical Research Associates oversee clinical trials, ensuring compliance and data integrity at trial sites. While both roles require a background in life sciences and related certifications, Medical Biotech emphasizes product development, whereas Clinical Research Associates concentrate on trial management and regulatory adherence.

What cities in Georgia are hiring for Medical Biotech jobs?

Cities in Georgia with the most Medical Biotech job openings:

Medical Biotech jobs near you
Infographic showing various Medical Biotech job openings in Georgia as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 16% Part Time, 1% Temporary, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $139,096 per year, or $66.9 per hour.

CRA 1, IQVIA Biotech

IQVIA

Marietta, GA

$71K - $145K/yr

Full-time

Re-posted 6 hours ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring highquality clinical data, and maintaining study integrity.

Key Responsibilities

As a CRA I, you will conduct various types of monitoring visits-including site selection, initiation, routine monitoring, and closeout visits-to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).

A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address sitelevel challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or startup activities based on study needs.

Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, followup letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.

Qualifications

  • Bachelor's degree required; a scientific or healthcare discipline is preferred.
  • 6 months -2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
  • Basic knowledge of clinical research regulations (GCP/ICH).
  • Ability to travel as required by the project.

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 $71,900.00 - $145,300.00. 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.

What IQVIA employees say

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Hours and flexibility

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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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