{"id":3230,"date":"2023-01-19T02:53:58","date_gmt":"2023-01-18T21:23:58","guid":{"rendered":"https:\/\/pharmaceuticalcarrier.com\/?post_type=job_listing&#038;p=3230"},"modified":"2023-07-19T03:27:45","modified_gmt":"2023-07-18T21:57:45","slug":"project-manager-in-revana-therapeutics-belfast-united-kingdom","status":"publish","type":"job_listing","link":"https:\/\/pharmaceuticalcarrier.com\/index.php\/job\/project-manager-in-revana-therapeutics-belfast-united-kingdom\/","title":{"rendered":"Project Manager in Revana Therapeutics Belfast United kingdom"},"content":{"rendered":"<p><strong>Position Title:<\/strong> Program\/Project Manager<\/p><div class=\"pharm-content\" id=\"pharm-3767661714\"><script async src=\"\/\/pagead2.googlesyndication.com\/pagead\/js\/adsbygoogle.js?client=ca-pub-8402705006112223\" crossorigin=\"anonymous\"><\/script><ins class=\"adsbygoogle\" style=\"display:block;\" data-ad-client=\"ca-pub-8402705006112223\" \ndata-ad-slot=\"7652789694\" \ndata-ad-format=\"auto\"><\/ins>\n<script> \n(adsbygoogle = window.adsbygoogle || []).push({}); \n<\/script>\n<\/div>\n<p><strong>Reports to:<\/strong> CEO<\/p>\n<p><strong>Department:<\/strong> R&amp;D Location Belfast, Northern Ireland<br \/>\nIssue Date January 2023<\/p>\n<p><strong>Introduction<\/strong><br \/>\nRe-Vana Therapeutics, founded in 2016 and incorporated in both the U.K. and U.S. is a spin-out<br \/>\nfrom Queen\u2019s University Belfast (QUB) Northern Ireland. We are developing innovative and<br \/>\nproprietary biodegradable sustained-release technologies for the delivery of biologics and small<br \/>\nmolecules drugs, with a focus on ophthalmic indications.<br \/>\nOur value proposition is the ability to develop \u201ccustomized\u201d sustained-release implants capable of<br \/>\ndelivering both biologics and small molecules for as long as 6 months or more, thus reducing the<br \/>\nfrequency of ocular injections and reducing or eliminating the need for topical eye drops. The<br \/>\nsustained delivery of biologic drugs is recognized as one of the major unmet needs within<br \/>\nophthalmology. Currently, ophthalmic biologic drugs represent a $14B market worldwide with growth<br \/>\nprojections reaching more than $22B by 2024.<br \/>\nOur dual strategy includes the internal development of sustained-release therapeutics alongside the<br \/>\ndevelopment of external strategic collaborations with major pharmaceutical partners. To date ReVana has achieved significant progress and global awareness, raising seed money in 2017, a preSeries A in 2020 and a Series A in 2022 that included leading U.S. Ophthalmic and U.K. Venture<br \/>\nCapital Investors. We have been awarded two significant Innovate U.K. government grants for the<br \/>\ndevelopment of sustained-release ocular biologics. In 2022, we were awarded the prestigious<br \/>\nOphthalmic Innovation Summit Retina Award for \u201cDrug Delivery Innovation\u201d and the Belfast<br \/>\nChamber \u201cBusiness Innovation\u201d company of the year. In addition, Re-Vana has established a<br \/>\ncompelling Scientific Advisory Board (SAB) that includes global ophthalmic opinion leaders.<br \/>\nWe are seeking to further strengthen the team by hiring a full-time, Program Manager to develop and<br \/>\nmanage an internal Project Management system within the company.<br \/>\nThe successful candidate will be a key member of the Belfast based team. Reporting to the CEO,<br \/>\nhe\/she will work extensively with the COO, CTO and the internal scientific team.<br \/>\n.<br \/>\nThis is an outstanding opportunity to help build and contribute significantly to the strategic success of<br \/>\na well-capitalized, highly innovative startup company within a multibillion dollar market potential.<\/p>\n<p><strong>Description of Role:<\/strong><br \/>\nTo Project Manage the non-clinical product development and strategic collaboration programs in<br \/>\nsupport of the company\u2019s strategic plan. Prepare and provide strategic and tactical planning models,<br \/>\nadvice and direction to the scientific team to deliver all agreed technical and therapeutic programs<br \/>\non time, supporting the R&amp;D team to achieve set objectives.<\/p>\n<p><strong>Responsibilities:<\/strong><br \/>\n\u2022 Overall responsibility for internal non-clinical and strategic collaboration programs to ensure high<br \/>\nquality products are developed in alignment with strategic goals, industry best-practices, and<br \/>\nregulatory requirements and guidance\u2019s<br \/>\n\u2022 Management of appointed CDMO(s) for development of combination drug\/medical device(s)<br \/>\n\u2022 Develop and manage department-level budgets and product development timelines<br \/>\n\u2022 Contribute technical and industry knowledge to the scientific and senior management team<br \/>\nworking to develop strategic plans for product and portfolio development, applying technical and<br \/>\nindustry knowledge<br \/>\n\u2022 Evaluate trends and technologies within polymer based biodegradable drug delivery therapeutics<br \/>\nmaterials, and process technology that potentially address unmet clinical needs for new<br \/>\nprograms and\/or product development challenges for existing programs<br \/>\n\u2022 Develops R&amp;D and Operations reports for senior management and Board members<br \/>\n\u2022 Work with Re-Vana leadership to develop a pro-active, team-oriented culture<br \/>\n\u2022 Develop and mentor scientific team members to be empowered and continually improve<br \/>\nperformance and achieve personal development goals<br \/>\n\u2022 Apply scientific, therapeutic and technical knowledge of drug\/device combination product<br \/>\nindustry to assist company in development of new products and enhancements to existing<br \/>\nproducts<br \/>\n\u2022 Contribute to the intellectual property of the company via invention and patent applications<br \/>\n\u2022 Demonstrate a primary commitment to patient safety and product quality by maintaining<br \/>\ncompliance with Company\u2019s quality policies and procedures<br \/>\n\u2022 Other activities to support the Company in meeting its operational, strategic, and financial goals<\/p>\n<p><strong>Requirements:<\/strong><br \/>\n\u2022 B.Sc. in science or engineering discipline (MS or PhD preferred)<br \/>\n\u2022 At least 5 years of progressively responsible positions in product development of medical<br \/>\ndevices, pharmaceutical products, and\/or drug\/device combination products<br \/>\n\u2022 5+ years of prior project management experience<br \/>\n\u2022 Able to work effectively within the confines of a regulated, quality-system driven, FDA-monitored<br \/>\ncombination product environment required<br \/>\n\u2022 Excellent communication, leadership, problem-solving, and time management skills<br \/>\n\u2022 Ability to effectively interact with all levels of professionals, backgrounds, and perspectives<br \/>\n\u2022 Solid knowledge and background in the design &amp; development of drug delivery technologies and<br \/>\nmedical devices from concept to commercialization strongly preferred<br \/>\n\u2022 Experience with drug\/device combination product and polymers strongly preferred<br \/>\n\u2022 Product development program\/project management from concept to commercialization preferred<br \/>\n\u2022 Experience managing local and virtual teams<\/p>\n<p><strong>Additional<\/strong><br \/>\nRemuneration to be based on a fixed salary, bonus and stock options relevant to a startup<br \/>\norganization<br \/>\n<strong>Contact<\/strong><br \/>\nPlease send an updated CV with supporting letter to<br \/>\nMichael O\u2019Rourke CEO<br \/>\nmor@revanatx.com<\/p>\n<blockquote class=\"wp-embedded-content\" data-secret=\"4CaucPZwA0\"><p><a href=\"https:\/\/www.revanatx.com\/\">Home<\/a><\/p><\/blockquote>\n<p><iframe loading=\"lazy\" class=\"wp-embedded-content\" sandbox=\"allow-scripts\" security=\"restricted\" style=\"position: absolute; clip: rect(1px, 1px, 1px, 1px);\" title=\"&#8220;Home&#8221; 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