Vitro Jobs in Usa

Retina Specialist Physician Opportunity near LONG ISLAND CITY, NY We are currently looking for a skilled physician specializing in ophthalmology with a focus on medical and/or surgical retina to join our team in providing exceptional patient care.

This is a permanent position, and we welcome applications from both experienced individuals with 2 years or more of experience and newly trained retina fellows.

Ideal Candidate Qualities: Ability to diagnose and treat a diverse range of vitro-retinal conditions to enhance patient outcomes.

Competency in diagnosis and treatment to maintain high standards of patient care and safety.

Patient-centered approach, ensuring a positive patient experience.

Excellent communication skills.

Interest in population health management and value-based care.

Responsibilities: Review patient medical history, reports, and examination results.

Conduct retinal examinations and interpret various tests (OCT, photos, fluorescein angiograms, etc.).

Evaluate, diagnose, and provide treatment for a variety of vitro-retinal conditions.

Perform office-based procedures, including intravitreal injections, photocoagulation, and laser procedures.

For surgical retinal specialists, conduct weekly outpatient surgical procedures such as vitrectomy, scleral buckling, membrane peeling, and macular hole repair.

Prescribe medications and develop ongoing treatment plans.

Collaborate with primary care providers, internal and external optometrists and ophthalmologists.

Provide relationship-centered care, considering psychosocial and physical patient needs.

Maintain accurate medical records.

Communicate effectively with the clinical team.

Qualifications: Doctor of Medicine (MD), Doctor of Osteopathic Medicine (DO), or foreign equivalent.

Completion of a three-year postgraduate medical training program in ophthalmology from a U.S.

accredited residency.

Completion of a medical or medical-surgical retina fellowship, preferably registered with AUPO-FCC.

Board Eligible/Board Certified in Ophthalmology.

Current, unrestricted New York State license or eligibility for licensure.

Active Drug Enforcement Agency (DEA) registration or eligibility.

Active Medicare/Medicaid Enrollment or eligibility.

Basic Life Support (BLS) required; Advanced Cardiac Life Support (ACLS) strongly preferred.

Strong communication skills, both oral and written.

Comfortable with Electronic Medical Record (EMR) system and Microsoft Office.

Job ID: j-201501

Associate Scientist

Location: Durham, NC

Focus: Retinal Disease & AAV Platforms

Role Summary

We are seeking a versatile Associate Scientist to drive the design and execution of molecular and cell biology experiments centered on AAV-based retinal gene therapies. This role is a hybrid of innovative R&D and operational leadership; you will transition between conducting high-stakes experiments at the bench and overseeing laboratory operations, including budget management, vendor sourcing, and regulatory compliance.

Primary Responsibilities

• Experimental Design & Execution: Develop and maintain complex mammalian cell models (including iPSC, human, and animal lines) to support in vitro disease modeling.
• Gene Therapy Validation: Lead molecular assays to evaluate the efficacy of AAV vectors and small molecules using dPCR, protein quantification, and functional potency assays.
• Data Strategy: Meticulously document, interpret, and present experimental findings to cross-functional scientific teams.
• Laboratory Operations: Manage the R&D budget, oversee procurement, coordinate with external service providers, and maintain instrumentation to ensure a seamless research environment.
• Quality & Compliance: Author and refine SOPs, technical reports, and protocols while ensuring the lab strictly adheres to safety and regulatory standards.

Technical Qualifications

• Cellular Modeling: Extensive hands-on experience with mammalian and iPSC culture. (Specific experience with retinal models or potency assays is highly preferred).
• Molecular Toolbox: Proficiency in cloning, qPCR/dPCR, Western Blotting, and ELISA.
• Digital Fluency: Advanced skill in data analysis and design software, including GraphPad Prism, SnapGene, and the MS Office Suite.
• Operational Mindset: Proven ability to manage lab inventory and equipment in a fast-paced, collaborative startup or biotech environment.

Education & Experience

• Degree: B.S. or M.S. in Neuroscience, Ophthalmology, Molecular Biology, Biomedical Engineering, or a related discipline.
• Experience: A minimum of 4 years of hands-on laboratory experience.
• Preferred Skills: Direct experience with viral vectors (AAV/Lentivirus) and the full lifecycle of iPSC management (culture, clone selection, and banking).

• Support external screening data operations and vendor coordination to ensure accurate, timely data delivery for scientific decision-making.

• Maintain and update external screening data repositories and vendor-specific portals.
• Process screening requests, validate and QC data deliverables, and distribute accurate data to scientists.
• Receive, format, and publish screening data using standardized data-loading tools and templates.
• Register and maintain vendor profiles and project records in designated systems.
• Maintain and update reference/control compound lists and screening protocols.
• Request registration of new control/reference compounds as needed.
• Adhere to established data handling standards and maintain clear documentation for audits and reporting.

• Bachelor’s degree in Life Sciences, Data Management, or a related field (or equivalent experience).
• Experience in scientific data workflows and management.
• Lab experience with in vitro screening assays desired.

• Strong attention to detail with excellent organizational and communication skills.
• Ability to manage multiple priorities in a fast-paced, cross-functional environment.
• Collaboration: Builds strong relationships across teams and with external partners.
• Adaptability: Responds effectively to changing priorities and evolving processes.
• Accountability: Takes ownership of deliverables and follows through to completion.
• Customer Focus: Anticipates the needs of scientists and stakeholders to improve service quality.
• Continuous Learning: Seeks opportunities to enhance knowledge of tools and best practices.

  External Screening Data Support Specialist

  Location: Groton CT or La Jolla, CA
  External Research Solutions (ERS) supports scientific innovation by managing external screening partnerships and ensuring seamless data integration between internal teams and external vendors. Our mission is to enable high-quality, efficient research through robust data operations, strong vendor collaboration, and disciplined data governance.
  

  Role Overview

• Support external screening data operations and vendor coordination to ensure accurate, timely data delivery for scientific decision-making.

• Key Responsibilities

• Maintain and update external screening data repositories and vendor-specific portals.
• Process screening requests, validate and QC data deliverables, and distribute accurate data to scientists.
• Receive, format, and publish screening data using standardized data-loading tools and templates.
• Register and maintain vendor profiles and project records in designated systems.
• Maintain and update reference/control compound lists and screening protocols.
• Request registration of new control/reference compounds as needed.
• Adhere to established data handling standards and maintain clear documentation for audits and reporting.

• Qualifications

• Bachelor’s degree in Life Sciences, Data Management, or a related field (or equivalent experience).
• Experience in scientific data workflows and management.
• Lab experience with in vitro screening assays desired.

• Competencies & Behavioral Skills

• Strong attention to detail with excellent organizational and communication skills.
• Ability to manage multiple priorities in a fast-paced, cross-functional environment.
• Collaboration: Builds strong relationships across teams and with external partners.
• Adaptability: Responds effectively to changing priorities and evolving processes.
• Accountability: Takes ownership of deliverables and follows through to completion.
• Customer Focus: Anticipates the needs of scientists and stakeholders to improve service quality.
• Continuous Learning: Seeks opportunities to enhance knowledge of tools and best practices.