nonclinical

ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA.At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different nationalities is committed to pioneering...

Proclinical is partnering with a clinical-stage biotechnology company to identify a Director/Senior Director of Toxicology & Nonclinical Safety in Leiden, NL. The role leads nonclinical safety strategy, oversees GLP toxicology programs and supports regulatory submissions.Based in Leiden with four on-site days per week, the senior leader will manage CRO...

Director / Senior Director of Toxicology€95,000 - €135,000 + Bonus + Stock OptionsBased in Leiden, NL (4 days on site a week)Are you looking to define and execute toxicology strategies that enable the progression of innovative RNA therapeutics from discovery through clinical development?Proclinical is working with a clinical-stage biotechnology company...

ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different nationalities is committed to pioneering...

ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different nationalities is committed to pioneering...

ProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different nationalities is committed to pioneering...

ProQR Therapeutics N.V. is seeking a Director of Toxicology to lead nonclinical safety assessment across the Translational Development portfolio.You will define strategies, drive GLP studies with CROs, and ensure robust safety packages for regulatory submissions, working with cross-functional teams to advance RNA therapeutics from discovery to development....

About Ocugen Netherlands B.V.Ocugen Netherlands B.V. is the European subsidiary of Ocugen, Inc., a U.S.-based biotechnology company focused on developing innovative gene and cell therapies and vaccines to improve patients' lives. Our work includes advancing novel treatments for serious retinal diseases with significant unmet medical needs.We are establishing...

Manager / Associate Director Regulatory Affairs Operations & SubmissionsIs dit uw volgende baan? Lees de volledige omschrijving hieronder om erachter te komen en aarzel niet om te solliciteren.Department DevelopmentProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge,...

ROLE OVERVIEWAn exciting opportunity for a Regulatory Affairs Project Manager to join our client, a leading organisation within the pharmaceutical, biotechnology and life sciences sector. This role will lead and coordinate regulatory projects across the product lifecycle, working closely with Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC),...

DescriptionAbout Ocugen Netherlands B.V. Ocugen Netherlands B.V. is the European subsidiary of Ocugen, Inc., a U.S.-based biotechnology company focused on developing innovative gene and cell therapies and vaccines to improve patients’ lives. Our work includes advancing novel treatments for serious retinal diseases with significant unmet medical...

The role: The Senior Director Non-Clinical Development determines and executes the strategy of Pharming's non-clinical development programs for Pharming's biopharmaceutical products and leads the non-clinical team. Responsibilities include non-clinical development of all of Pharming’s products including the modules for the regulatory filing and ensure...

pProclinical is partnering with a clinical-stage biotechnology company to identify a Director/Senior Director of Toxicology Nonclinical Safety in Leiden, NL. The role leads nonclinical safety strategy, oversees GLP toxicology programs and supports regulatory submissions. /ppBased in Leiden with four on-site days per week, the senior leader will manage CRO...

h3Director / Senior Director of Toxicology /h3 /brp€95,000 - €135,000 + Bonus + Stock Options /p /brpBased in Leiden, NL (4 days on site a week) /p /brpAre you looking to define and execute toxicology strategies that enable the progression of innovative RNA therapeutics from discovery through clinical development? /p /brpProclinical is working with a...

ppProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in Cambridge, Massachusetts, USA. At ProQR, we are on a mission to edit RNA, treat disease and change lives. A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different nationalities is committed to pioneering...

h3Manager / Associate Director Regulatory Affairs Operations Submissions /h3 pDepartment Development /p pProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. /A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different...

h3Manager / Associate Director Regulatory Affairs Operations Submissions /h3 pDepartment Development /p pProQR Therapeutics is a NASDAQ-listed biotechnology company headquartered in Leiden, the Netherlands with an office in and Cambridge, Massachusetts, USA. /A team of 180+ enthusiastic ProQRians from all walks of life and more than 30 different...

pbThe role: /b The Senior Director Non-Clinical Development determines and executes the strategy of Pharming's non-clinical development programs for Pharming's biopharmaceutical products and leads the non-clinical team. Responsibilities include non-clinical development of all of Pharming’s products including the modules for the regulatory filing and ensure...

  VP / SVP Research and Development The opportunity A Forbion portfolio company is seeking an accomplished scientific leader to join its R&D organisation as VP/SVP Research & Development. The company is a science-led European biotech developing differentiated biologic medicines for serious diseases. It is advancing an innovative portfolio toward the clinic...

  Job Title:       Director, Regulatory AffairsLocation:      Amsterdam, Netherlands, United Kingdom- Remote ConsideredReports to:  Vice President, Regulatory Affairs   Position Summary: Ready to lead regulatory strategy for innovative products that can improve health worldwide? As Regulatory Affairs Director, you will guide global regulatory...