36 results for Regulatory Consultants
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Regulatory Affairs Consultant Safety/Labelling
Poland, Remote Romania, Remote Consulting -
Principal Regulatory Affairs Consultant - CMC small molecule
United Kingdom, Remote Serbia, Remote; Serbia, Belgrade; Romania, Remote; Romania, Bucharest, Metropolis Center; Hungary, Remote; Hungary, Budapest; Ireland, Remote; Ireland, Dublin; Spain, Remote; Spain, Madrid; Italy, Milan; Italy, Remote; Poland, Remote; Poland, Warsaw, Business Garden; Croatia, Remote; Croatia, Zagreb Consulting -
Regulatory Affairs Consultant - Switzerland & Germany
Switzerland, Remote Consulting -
Senior Associate, Regulatory & Access Consulting
Japan, Remote Japan, Osaka, Remote Consulting -
Senior Regulatory Affairs Consultant (Project Leader) /薬事部門のプロジェクトリーダー
Japan, Tokyo Japan, Osaka Consulting -
Regulatory Affairs Project Lead (MAAs)
Romania, Remote Serbia, Remote; Serbia, Belgrade; Romania, Bucharest, Metropolis Center; Hungary, Remote; Hungary, Budapest; Czech Republic, Remote; Czech Republic, Prague; Lithuania, Remote; Lithuania, Vilnius; Poland, Remote; Poland, Warsaw, Business Garden; Croatia, Remote; Croatia, Zagreb Consulting -
Regulatory Affairs Associate
Poland, Warsaw, Business Garden Romania, Remote; Croatia, Remote Consulting -
Associate Director, Regulatory Affairs
India, Remote Consulting -
Regulatory Affairs - Publishing
Mexico, Remote Consulting -
Regulatory Affairs - Publishing
Argentina, Remote Consulting -
Senior Regulatory Affairs Manager - CMC (various locations)
United Kingdom, Remote Serbia, Remote; Serbia, Belgrade; Romania, Remote; Romania, Bucharest, Metropolis Center; Hungary, Remote; Hungary, Budapest; Ireland, Remote; Ireland, Dublin; United Kingdom, London, Gridiron; Spain, Remote; Spain, Madrid; Italy, Milan; Italy, Remote; Poland, Remote; Poland, Warsaw, Business Garden; Croatia, Remote; Croatia, Zagreb Consulting -
Regulatory Manager - CMC biologics (various European locations)
United Kingdom, Uxbridge Serbia, Remote; Serbia, Belgrade; Romania, Remote; Romania, Bucharest, Metropolis Center; Hungary, Remote; Hungary, Budapest; Poland, Cracow; Ireland, Remote; Ireland, Dublin; Spain, Remote; Spain, Madrid; Italy, Milan; Italy, Remote; Czech Republic, Remote; Czech Republic, Prague; United Kingdom, Uxbridge, Remote; Lithuania, Remote; Lithuania, Vilnius; Poland, Remote; Poland, Warsaw, Business Garden; Belgium, Remote; Belgium, Wavre, Parc Des Collines; Croatia, Remote; Croatia, Zagreb Consulting -
Local Qualified Person for Pharmacovigilance (QPPV) Freelancer - TALENT POOL
Netherlands, Remote Estonia, Remote; Slovakia, Remote; Greece, Remote; Germany, Berlin, Remote; Switzerland, Remote; Australia, Brisbane; Hungary, Remote; Portugal, Remote; Italy, Remote; France, Paris, Remote; Czech Republic, Remote; Israel, Remote; Latvia, Remote; Bulgaria, Remote; Turkey, Remote; Lithuania, Remote; Poland, Remote; Belgium, Remote; Croatia, Remote Clinical Logistics -
Medical Director - Ophthalmology
Serbia, Remote Netherlands, Remote; Switzerland, Remote; South Africa, Bloemfontein, Remote; Romania, Remote; Hungary, Remote; Ireland, Remote; Denmark, Remote; Spain, Remote; Italy, Remote; France, Paris, Remote; Czech Republic, Remote; Israel, Remote; Sweden, Remote; Georgia, Remote; Turkey, Remote; United Kingdom, Uxbridge, Remote; Lithuania, Remote; Poland, Remote; Belgium, Remote; Croatia, Remote Medical Sciences -
Senior Medical Director - Pharmacovigilance/Drug Safety
United Kingdom, Remote Serbia, Remote; South Africa, Bloemfontein, Remote; Romania, Remote; Hungary, Remote; Ireland, Remote; Spain, Remote; Italy, Remote; Czech Republic, Remote; Israel, Remote; Turkey, Remote; Lithuania, Remote; Poland, Remote; Croatia, Remote Medical Sciences
17 Content Pages Found
- Discover the qualifications, experience, and skills needed to be a successful Regulatory Affairs Consultant
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Meet Irene, Senior Regulatory Affairs Consultant
Explore Irene's journey as a Senior Regulatory Affairs Consultant at Parexel, as she is bringing life-changing treatments to patients, passion for clinical research, and embodiment of Parexel's patient-centric approach. -
Regulatory Affairs Jobs at Parexel
Help shape the future of drug development, streamline approval processes, and safeguard patient well-being. Advance your career and explore Parexel's diverse roles in Regulatory Strategy, Regulatory Affairs, Compliance, Consulting, and more. -
Regulatory Affairs Jobs at Parexel
Help shape the future of drug development, streamline approval processes, and safeguard patient well-being. Advance your career and explore Parexel's diverse roles in Regulatory Strategy, Regulatory Affairs, Compliance, Consulting, and more. -
Meet Steve, a VP Technical of Regulatory Strategy
Steve is working to guide clients through the regulatory journey from initial clinical trials to achieving market success. Read more about what a day in the life of a VP Technical at Parexel looks like and how Steve can utilize his FDA background and apply his skills to his current position. -
Meet Mwango: SVP & Global Head of Regulatory Strategy
Mwango shares how she came to Parexel after spending 16 years at the FDA to experience the process and considerations from the drug developer’s perspective. Read about her role as a VP-Technical and what valuable advice she offers to those looking to work With Heart™. -
What does a Regulatory Affairs Consultant do?
Explore the Regulatory Affairs Consultant role at Parexel: key responsibilities, tools, collaboration, career growth, and work flexibility in clinical research. -
Meet Sheryl: Principal Regulatory Affairs Consultant, Regulatory Strategy
Sheryl, Principal Regulatory Affairs Consultant, talks about why she joined Parexel and how she keeps the patient first. -
Meet Ben: Senior Regulatory Affairs Consultant
Ben provides and insight into his role as a regulatory affairs consultant. He also talks openly about being part of the LGBTQ+ community and how Parexel's flexible work arrangements help him as a single father. -
Meet Simona: Principal Consultant, Regulatory & Access
Simona shares how Parexel has supported her career development, the day-to-day activities of being a Principal Consultant at R&A, and much more! -
Our work culture
Learn about our culture, perks, learning opportunities, and our corporate responsibility approach. Parexel's compassionate and results-driven work culture prioritizes patient care and employee growth. -
Meet Jo, VP Consulting, navigating FDA inspections
Discover how Jo leverages her FDA background to guide pharma companies through inspections, accelerating patient access to life-changing medicines. -
Meet Jessica, Senior Director, Integrated Solutions Strategy, CRS Solutions Consultant
Jessica has made the unique commitment to participate in a clinical trial once a year and she is on her 10th study! Read more about Jessica and how she continues to push the clinical trials industry further; Discover what Jessica is most proud of during her time at Parexel, and what she does to always put "Patients First". -
Medical Writing Opportunities
Join Parexel's global team of 700+ medical writers. Deliver impactful, high-quality content and advance your career in medical writing. -
Meet Lynne: Senior Vice President & Head of RCS Global Compliance
Lynne, Senior Vice President & Head of RCS Global Compliance, shares her journey at Parexel after leaving the FDA
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