... development, preclinical and clinical research, regulatory affairs, and market access and ... Coordinate with Study Directors and operational personnel to resolve documentation deficiencies ...
... development, preclinical and clinical research, regulatory affairs, and market access and ... Coordinate with Study Directors and operational personnel to resolve documentation deficiencies ...
Educate medical students in Pathology across a 2-year preclinical curriculum. * Collaborate with ... Participate in development and facilitation of clinical case presentations for active learning as ...
Educate medical students in Pathology across a 2-year preclinical curriculum. * Collaborate with ... Participate in development and facilitation of clinical case presentations for active learning as ...
Educate medical students in Pathology across a 2-year preclinical curriculum. * Collaborate with ... Participate in development and facilitation of clinical case presentations for active learning as ...
Educate medical students in Pathology across a 2-year preclinical curriculum. * Collaborate with ... Participate in development and facilitation of clinical case presentations for active learning as ...
Educate medical students in Pathology across a 2-year preclinical curriculum. * Collaborate with ... Participate in development and facilitation of clinical case presentations for active learning as ...
Educate medical students in Pathology across a 2-year preclinical curriculum. * Collaborate with ... Participate in development and facilitation of clinical case presentations for active learning as ...
Director Preclinical Development information
What is a director preclinical development?
A Director of Preclinical Development oversees the early-stage research and testing of drug candidates before they enter clinical trials. They manage preclinical studies, ensuring regulatory compliance, safety, and efficacy assessments. This role involves coordinating with cross-functional teams, external partners, and regulatory agencies to advance promising compounds. Strong expertise in toxicology, pharmacology, and regulatory guidelines is essential. The director plays a key role in shaping the preclinical strategy to support successful drug development.
What are the key skills and qualifications needed to thrive in the director preclinical development position, and why are they important?
To thrive as a Director Preclinical Development, you need deep expertise in pharmaceutical or biotechnology research, strong project management abilities, and an advanced degree (Ph.D., Pharm.D., or equivalent) in a life sciences field. Familiarity with regulatory guidelines (such as GLP), experience using data management and statistical analysis software, and prior leadership roles in preclinical studies are essential. Exceptional communication, problem-solving, and team leadership skills set candidates apart in managing multidisciplinary teams and collaborative projects. These competencies are crucial for successfully guiding drug candidates through preclinical stages while ensuring regulatory compliance and timely project delivery.
What are the typical responsibilities and team dynamics for a director preclinical development?
A Director of Preclinical Development is responsible for overseeing the planning, execution, and management of preclinical research programs, ensuring that studies meet scientific, regulatory, and project milestones. You will typically work with cross-functional teams including toxicologists, pharmacologists, regulatory affairs professionals, and external partners, fostering collaboration throughout the drug development process. The role often involves reviewing study designs and data, preparing regulatory submissions, and providing strategic direction to advance compounds toward clinical testing. Working closely with upper management, you'll play a key part in shaping research priorities and resource allocation. This position offers significant influence over drug development strategies and opportunities for advancement to higher executive or scientific leadership roles.
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What job categories do people searching Director Preclinical Development jobs in Georgia look for? The top searched job categories for Director Preclinical Development jobs in Georgia are:
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
Required Qualifications
Preferred Qualifications
Location
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.
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.
About Veranex
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Raleigh, NC, US
Year founded
2021