
51 - 200 employees
𧬠Biotechnology
π Pharmaceuticals
Biotechnology β’ Pharmaceuticals
Neurotech Pharmaceuticals, Inc. is a private biotechnology company focused on developing transformative therapies for chronic eye diseases, with a primary therapeutic focus on retinal disorders such as Macular Telangiectasia (MacTel) Type 2. The company develops and commercializes an Encapsulated Cell Therapy (ECT) platform that delivers Ciliary Neurotrophic Factor (CNTF) to protect photoreceptors and slow vision loss; its lead product ENCELTO (revakinagene taroretcel-lwey / NT-501) has received FDA approval for treating MacTel. Neurotech conducts R&D, clinical development, regulatory activities, and commercialization efforts targeting retinal neuroprotection and vision preservation.
π 6 days ago
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51 - 200 employees
𧬠Biotechnology
π Pharmaceuticals
Biotechnology β’ Pharmaceuticals
Neurotech Pharmaceuticals, Inc. is a private biotechnology company focused on developing transformative therapies for chronic eye diseases, with a primary therapeutic focus on retinal disorders such as Macular Telangiectasia (MacTel) Type 2. The company develops and commercializes an Encapsulated Cell Therapy (ECT) platform that delivers Ciliary Neurotrophic Factor (CNTF) to protect photoreceptors and slow vision loss; its lead product ENCELTO (revakinagene taroretcel-lwey / NT-501) has received FDA approval for treating MacTel. Neurotech conducts R&D, clinical development, regulatory activities, and commercialization efforts targeting retinal neuroprotection and vision preservation.
β’ Establish, manage, and maintain successful relationships with relevant healthcare entities including but not limited to, KOLs, HCPs, academic institutions, payors, patient organizations, etc. to serve as the education, research, and clinical/scientific informational resource. β’ Identify and engage in scientific exchange and develop strong scientific relationships with national, regional, and local key opinion leaders and experts. β’ Provide scientific presentations at company sponsored meetings such as advisory boards and external meetings such as managed care presentation as needed. β’ Attend national and regional medical/scientific meetings and symposia and engage in discussions with attendees as appropriate; attend scientific sessions and poster presentations, gather information, and summarizes findings; as appropriate, cultivate professional relationships from interactions at these meetings. β’ Ensure the appropriate dissemination of scientific information in a compliant, unbiased, and timely manner. β’ Respond to unsolicited medical and scientific requests for medical information in a compliant and timely manner; liaises with investigators on unsolicited requests for investigator-initiated research submission studies. β’ Sustain expertise in product/molecule data, disease state management, emerging therapies, and the competitive landscape. β’ Evaluate competitor research and information relevant to company therapeutic areas, objectives, activities, and product priorities; stay current on therapeutic advances; analyzes and applies relevant intelligence findings and presents data/insight to appropriate internal stakeholders. β’ Collaborate and work effectively across multi-disciplinary internal groups (Clinical, Regulatory, Commercial (Sales and Marketing), Legal, Compliance, etc.) to provide support medical/scientific and business objectives. This will include providing disease state, clinical and scientific training as requested across functional teams and providing input to management on therapeutic and research advances, business development opportunities/risks, and KOL feedback. β’ Maintain a thorough awareness of medical/clinical, regulatory, compliance, and quality issues and processes as they apply to the Companyβs therapeutic areas and adheres to, and supports the standards established by the company. β’ Completes accurate and timely submission of administrative reports, projects, expense reports, training, KOL documentation, conference reports, and all other required documentation; and other duties as assigned.
β’ A doctoral degree (MD, PharmD, PhD, OD or equivalent) is required. β’ Previous Medical Science Liaison experience in the pharmaceutical/biopharmaceutical industry is required. β’ Minimum of 4+ years MSL experience is required. β’ Ophthalmology experience strongly preferred; surgical device experience strongly preferred. β’ Knowledge of current regulatory guidelines to ensure corporate compliance in all activities, including those related to scientific interactions, unsolicited questions and clinical trials and research. β’ Behave in an ethical and professional manner, adhering to the company's guidelines and regulatory requirements. β’ Adept at building and maintaining relationships with key healthcare providers and other industry stakeholders. β’ Ability to manage multiple projects and initiatives simultaneously, and be able to organize, communicate, and prioritize work effectively. β’ Excellent interpersonal and communication skills are needed.
β’ Neurotech Pharmaceuticals provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Apply Nowπ 6 days ago
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πΊπΈ United States β Remote
π΅ $56.8k - $71k / year
π° Private Equity Round on 2020-12
β° Full Time
π Senior