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Preclinical Research Director Jobs in Decatur, GA

Emory University

Post Doctoral Fellow

Atlanta, GA

$47K - $64K/yr

Emory University is a leading research university that fosters excellence and attracts world-class ... The goal of this work is to evaluate an HIV cure strategy in a preclinical nonhuman primate model.

Emory University

Post Doctoral Fellow

Atlanta, GA · On-site

$47K - $64K/yr

Discover Your Career at Emory University Emory University is a leading research university that ... The goal of this work is to evaluate an HIV cure strategy in a preclinical nonhuman primate model.

Emory University

Post Doctoral Fellow

Atlanta, GA

$47K - $64K/yr

Discover Your Career at Emory University Emory University is a leading research university that ... The goal of this work is to evaluate an HIV cure strategy in a preclinical nonhuman primate model.

All JobsPreclinical Research JobsPreclinical Research Director JobsPreclinical Research Director Jobs in Decatur, GA

Preclinical Research Director information

See Decatur, GA salary details

$56.1K

$186.8K

$225K

How much do preclinical research director jobs pay per year?

As of Aug 6, 2026, the average yearly pay for preclinical research director in Decatur, GA is $186,792.00, according to ZipRecruiter salary data. Most workers in this role earn between $132,300.00 and $223,600.00 per year, depending on experience, location, and employer.

What is the difference between Preclinical Research Director vs Preclinical Scientist?

AspectPreclinical Research DirectorPreclinical Scientist
CredentialsAdvanced degrees (PhD, DVM) often required; leadership experienceTypically a PhD or Master's in relevant field
Work EnvironmentOversees teams in labs or R&D departments, strategic planningConducts experiments in laboratory settings, data analysis
Employer & Industry UsagePharmaceutical, biotech companies, CROsResearch institutions, biotech firms, pharma companies
Search & Comparison IntentUnderstanding leadership roles in preclinical researchDetails on scientific research and experimental work

The Preclinical Research Director focuses on leading research teams, strategic planning, and overseeing multiple projects, while the Preclinical Scientist is primarily involved in conducting experiments and analyzing data. Both roles require advanced scientific credentials, but the director's role emphasizes leadership and management within the preclinical research process.

What are the key skills and qualifications needed to thrive as a preclinical research director, and why are they important?

To thrive as a Preclinical Research Director, you need advanced knowledge in pharmacology, toxicology, and drug development, typically supported by a PhD or equivalent degree and extensive research experience. Familiarity with laboratory information management systems (LIMS), regulatory guidelines like GLP, and data analysis tools is essential. Strong leadership, project management, and communication skills help drive cross-functional teams and ensure alignment with strategic goals. These competencies are crucial for overseeing successful preclinical studies that support regulatory submissions and move drug candidates toward clinical trials.

What does a preclinical research director do?

A Preclinical Research Director oversees the planning, execution, and management of preclinical studies that assess the safety and efficacy of new drug candidates or medical devices before they are tested in humans. This role involves coordinating research teams, ensuring compliance with regulatory standards, managing budgets, and facilitating communication between cross-functional teams. They play a critical role in translating scientific discoveries into viable clinical candidates by guiding research strategy and ensuring the integrity and quality of preclinical data.

How does a preclinical research director typically collaborate with cross-functional teams during drug development projects?

A Preclinical Research Director works closely with multidisciplinary teams, including pharmacologists, toxicologists, regulatory affairs, and clinical development professionals. They facilitate communication between scientific staff and management, ensuring that preclinical studies align with project goals and regulatory requirements. Collaboration often involves regular meetings to review data, discuss study designs, and address any scientific or logistical challenges. This role is essential for integrating diverse expertise and driving projects efficiently toward clinical development milestones.
What are popular job titles related to Preclinical Research Director jobs in Decatur, GA? For Preclinical Research Director jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Preclinical Research Director jobs in Decatur, GA look for? The top searched job categories for Preclinical Research Director jobs in Decatur, GA are:
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Preclinical Research Director jobs near you
Infographic showing various Preclinical Research Director job openings in Decatur, GA as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 11% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $186,792 per year, or $89.8 per hour.

Preclinical Quality Assurance Technician 1

Veranex

Atlanta, GA • On-site

Full-time

Re-posted 2 days ago

Job description

Veranex's mission as an Innovation CRO is to improve patient outcomes by accelerating our clients' innovations to market. As the world's only end-to-end professional services firm focused on MedTech, we take clients' Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.
About This Role
The Preclinical Quality Assurance Technician 1 will primarily support study-level Quality Control activities at Veranex Preclinical Services in Atlanta. The position will be aligned with the Quality Assurance department and remain independent from study operations while working directly with study teams to support timely, accurate, and complete study documentation.
What You'll Do
  • Perform contemporaneous and detailed QC reviews of GLP and non-GLP study records, raw data forms, worksheets, logs and reports for completeness, accuracy, consistency, legibility, and compliance with SOP's and Good Documentation Practices (GDP).
  • Verify that study records contain all required signatures, dates, corrections, and supporting documentation.
  • Coordinate with Study Directors and operational personnel to resolve documentation deficiencies prior to QA inspections or record archival.
  • Support review of data tables, calculations, report components, study closure, and archival.
  • Conduct data reconciliation activities in collaboration with study personnel.
  • Maintain QC logs, issue trackers, and study-specific quality records.
  • Support audit and inspection readiness activities.
  • Assist with document control, quality documentation, training, and other QA/QC activities.

Required Qualifications
  • High school diploma or equivalent required; associate or bachelor's degree preferred.
  • Strong attention to detail, organization, consistency, and follow-through.
  • Strong written and verbal communication skills.
  • Ability to work independently and across functional teams.

Preferred Qualifications
  • Prior regulated laboratory, quality, research, healthcare, or document-control experience is beneficial but not required.

Location
  • This is an onsite position in Atlanta, GA.

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

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