44 results for Regulatory Consultants
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Regulatory Affairs Consultant
Taiwan, Remote Consulting, Regulatory Affairs -
(Senior) Director, Regulatory & Access Consulting
Japan, Remote Consulting, Regulatory Affairs -
Senior Regulatory Affairs Consultant / 薬事部門のプロジェクトマネジャー
Japan, Tokyo Japan, Osaka; Japan, Remote Consulting, Regulatory Affairs -
TALENT POOL: Regulatory Affairs Consultant - CMC biologics (home or office based)
United Kingdom, Remote Croatia, Remote; Croatia, Zagreb; Czech Republic, Prague; Czech Republic, Remote; Hungary, Budapest; Hungary, Remote; Ireland, Dublin; Ireland, Remote; Italy, Milan; Italy, Remote; Lithuania, Remote; Lithuania, Vilnius; Poland, Remote; Poland, Warsaw; Romania, Bucharest; Romania, Remote; Serbia, Belgrade; Serbia, Remote; Spain, Madrid; Spain, Remote Consulting, Regulatory Affairs -
Regulatory Affairs Associate CTA
Turkey, Istanbul Consulting, Regulatory Affairs -
Senior Regulatory Affairs Associate
South Korea, Seoul South Korea, Remote Consulting, Regulatory Affairs -
Senior / Vice President, Technical - Clinical Regulatory Affairs (Remote)
United States, Remote Consulting, Regulatory Affairs -
Senior Regulatory Affairs Associate (CMC)
South Korea, Seoul Consulting, Regulatory Affairs -
TALENT POOL - Regulatory Affairs Project Manager
United Kingdom, London Croatia, Remote; Croatia, Zagreb; Czech Republic, Prague; Czech Republic, Remote; Hungary, Budapest; Hungary, Remote; Ireland, Dublin; Ireland, Remote; Italy, Milan; Italy, Remote; Lithuania, Remote; Lithuania, Vilnius; Poland, Remote; Poland, Warsaw; Romania, Bucharest; Romania, Remote; Serbia, Belgrade; Serbia, Remote; Spain, Madrid; Spain, Remote; United Kingdom, Remote Project Leadership, Regulatory Affairs -
Senior Regulatory Affairs Associate (CMC)
Taiwan, Taipei Consulting, Regulatory Affairs -
Regulatory Affairs Associate, DENMARK - Talent Pool
Denmark, Remote Consulting, Regulatory Affairs -
Local Qualified Person for Pharmacovigilance (QPPV) Freelancer - TALENT POOL
Poland, Remote Australia, Brisbane; Belgium, Remote; Bulgaria, Remote; Croatia, Remote; Czech Republic, Remote; Estonia, Remote; France, Remote; Germany, Remote; Greece, Remote; Hungary, Remote; Israel, Remote; Italy, Remote; Latvia, Remote; Lithuania, Remote; Netherlands, Remote; Portugal, Remote; Slovakia, Remote; Switzerland, Remote; Turkey, Remote Clinical Logistics -
Medical Director - Ophthalmology
Spain, Remote Belgium, Remote; Croatia, Remote; Czech Republic, Remote; Denmark, Remote; Georgia, Remote; Hungary, Remote; Ireland, Remote; Israel, Remote; Italy, Remote; Lithuania, Remote; Netherlands, Remote; Poland, Remote; Romania, Remote; Serbia, Remote; South Africa, Remote; Sweden, Remote; Switzerland, Remote; Turkey, Remote; United Kingdom, Remote Medical Sciences -
Principal Medical Writer
Poland, Remote Poland, Warsaw Medical Writing -
Principal Medical Writer
Croatia, Remote Croatia, Zagreb Medical Writing
15 Content Pages Found
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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. -
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Discover the qualifications, experience, and skills needed to be a successful Regulatory Affairs Consultant -
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. -
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™. -
Meet Yuri, Regulatory Affairs Consultant
From regulatory dossiers to career growth, Yuri shares his journey in Chemistry, Manufacturing, and Controls (CMS) at Parexel. Explore the dynamic world of a regulatory affairs consultant through his professional experiences and insights. -
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! -
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. -
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, Senior 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. -
Medical Writing Opportunities
Join Parexel's global team of 700+ medical writers. Deliver impactful, high-quality content and advance your career in medical writing. -
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Careers in Oncology
Our dedicated people, innovative approaches, and culture of caring all work together to ease the journey for patients and investigators.
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