42 results for Regulatory Consultants
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Regulatory Affairs Consultant
Taiwan, Taipei Regulatory Affairs -
Regulatory Affairs Consultant (Biologics/Small Molecules)
India, Bengaluru Regulatory Affairs -
Regulatory Affairs Consultant / CMC薬事コンサルタント
Japan, Remote Japan, Tokyo Regulatory Affairs -
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 Regulatory Affairs -
Regulatory Affairs Consultant(CMC)
Taiwan, Remote Regulatory Affairs -
Senior Director, Regulatory & Access Consulting
Japan, Remote Regulatory Affairs -
Senior Regulatory Affairs Consultant - Labelling (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; Poland, Remote; Poland, Warsaw; Romania, Bucharest; Romania, Remote; Serbia, Belgrade; Serbia, Remote; Spain, Madrid; Spain, Remote Regulatory Affairs -
Regulatory Affairs Consultant - Global Labeling Lead (Temporary)
United States, Remote Regulatory Affairs -
Senior/Vice President, Technical (Clinical Regulatory)
United States, Remote Regulatory Affairs -
Senior Regulatory Affairs Associate - CMC biologics or vaccines
Romania, Bucharest Croatia, Remote; Croatia, Zagreb; Ireland, Remote; Poland, Remote; Poland, Warsaw; Romania, Remote; Serbia, Belgrade; Serbia, Remote; United Kingdom, Remote Regulatory Affairs -
Senior Regulatory Affairs Associate (Labelling)
India, Bengaluru Regulatory Affairs -
Senior Regulatory Affairs Associate (Biologics/Small Molecules)
India, Bengaluru Regulatory Affairs -
Senior Regulatory Affairs Associate - Artwork (home or office based)
Romania, Bucharest Croatia, Remote; Croatia, Zagreb; Czech Republic, Prague; Czech Republic, Remote; Hungary, Budapest; Hungary, Remote; Poland, Remote; Poland, Warsaw; Romania, Remote; Serbia, Belgrade; Serbia, Remote 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 -
Audit Specialist (Sponsor Audits and Inspections)
Lithuania, Remote Serbia, Belgrade; Serbia, Remote Quality Management
16 Content Pages Found
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What does an Initiation Clinical Research Associate do?
Explore the Initiation Clinical Research Associate (iCRA) role at Parexel: key responsibilities, tools, collaboration, career growth, and work flexibility in clinical research. -
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. -
Regulatory Affairs Consultants Qualifications, Experience, and Skills
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™. -
What does a Project Specialist do?
Explore the Project Specialist role at Parexel: key responsibilities, tools, collaboration, career growth, and work flexibility in clinical research. -
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 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 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. -
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. -
What Does a Statistical Programmer Do?
Explore the responsibilities, collaboration, and growth opportunities of a Statistical Programmer in the Clinical Research Industry.
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