SUSAN SCHNEIDER CONSULTING, LLC

Consulting services that support life-changing therapies through quality development solutions and expert guidance to biotechnology companies, pharmaceutical institutions, research organizations, entrepreneurs, investment firms, medical foundations, and advocacy groups.

Strategic Guidance. Clinical Leadership. Global Experience.​

FOCUSED ON GETTING PIVOTAL THERAPEUTIC OPTIONS TO MARKET TO POSITIVELY IMPACT HEALTHCARE AND QUALITY OF LIFE

Susan Schneider, Managing Member, is an executive leader and medical professional with nearly two decades of experience delivering high-quality early and late-stage clinical development programs in multiple disease indications. 

Key areas of consulting expertise include aligning global, cross-functional, scientific, clinical, and medical teams with a core focus on the design and implementation of all phases of clinical trials and post-marketing commitments. 

Strategic planning and execution of projects in multiple disease states transitioning from the preclinical stage through clinical development and product launch

Life cycle management of clinical development plans

Susan Schneider

Growth and development of gene therapy programs and drug delivery platforms

Business development due diligence and in-licensing opportunities 


Our areas of expertise serve biotechnology and pharmaceutical companies, health alliances, foundations and coalitions, contract research organizations, and advocacy groups worldwide. Susan Schneider Consulting, LLC provides support for growth objectives, development pipelines, and outreach opportunities

Clinical Research Medical Affairs Execution

Providing an essential component in seamlessly delivering on an organization’s strategic plan while ensuring the safety and efficacy of therapeutics and delivery platforms in development and incorporating real world experience.

Portfolio Strategy Input

Supporting the success of an organization’s initiatives through alignment between the pipeline, business needs, and actions required to achieve corporate goals.

Publication/
Presentation Planning

Assuring cohesive scientific and clinical data dissemination via formulation of a plan taking into consideration overall strategy, unmet medical needs, disease indication under study, current clinical practice, compliance, and timely communications,

Product Launch Readiness

Participating in an organization’s approach to preparedness in launching a new product by collaboration across functions with a focus on leading scientific and medical education and training, providing clinical expertise, and liaising on patient needs.

Professional Experience

Dr. Schneider, Managing Member, brings a wealth of experience to consulting opportunities, having held a broad spectrum of pharmaceutical and biotechnology positions including Medical Director, Therapeutic Area Head, Medical Advisor, Faculty Member, Senior Vice President Clinical Development Ophthalmology, and Chief Medical Officer

Education

Unique insights and learning perspectives acquired through a solid academic base:

M.D., Medical College of Pennsylvania

BA, The University of Pennsylvania

A strong clinical foundation via solid training in ophthalmology:

Fellowship, Ocular Oncology, Wills Eye Hospital

Fellowship, Ophthalmic Pathology, Wilmer Eye Institute

Residency, Ophthalmology, Medical College of Virginia

Clinical Plans, Study Designs, & Protocol Development

Reliable solutions for ensuring well-executed and successful clinical trials

Clinical Plans, Study Designs, & Protocol Development

Reliable solutions for ensuring well-executed and successful clinical trials

Clinical Trial Operational Execution

Well-crafted targeted strategies for recruitment and enrollment to ensure effective and efficient clinical trial completion

Clinical Trial Operational Execution

Well-crafted targeted strategies for recruitment and enrollment to ensure effective and efficient clinical trial completion

Data Monitoring & Oversight

Employing high-quality and timely data analysis and interpretation for clinical trials

Data Monitoring & Oversight

Employing high-quality and timely data analysis and interpretation for clinical trials

Clinical Regulatory Submission Representation

Optimal clinical regulatory strategies, input, and guidance throughout the submission process

Clinical Regulatory Submission Representation

Optimal clinical regulatory strategies, input, and guidance throughout the submission process

Advisory Oversight & Advocacy Guidance

Oversight in navigating healthcare settings to empower the decision-making process and to best reflect the patient journey in clinical development

Advisory Oversight & Advocacy Guidance

Oversight in navigating healthcare settings to empower the decision-making process and to best reflect the patient journey in clinical development

Presentation & Publication Planning

Establishing a format for scientific representation of data and outcomes from research, clinical development, and medical affairs

Presentation & Publication Planning

Establishing a format for scientific representation of data and outcomes from research, clinical development, and medical affairs

Committed to providing expert guidance and innovative solutions for developing important therapeutic options by supplying customized consulting services with excellence, integrity, and collaboration.

Your partner in a wide range of consulting possibilities.


Thank you for your interest. To learn more, please contact us.

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