Consultant - Regulatory Consulting ( Pharma / CMC )

Job description

We are looking for a Regulatory Affairs, Consultant to join our Regulatory Consulting Team. This is an amazing opportunity to work on regulatory consulting projects. We have a great skill set in data monitoring, content writing and consulting for multiple domains- regulatory submissions, clinical trials, marketing authorization applications (MAA), chemistry manufacturing and controls (CMC), CMC variations, pharmacovigilance projects, and regulatory strategy, among others, and we would love to speak with you if you have any of the skills or expertise in the regulatory affairs and consulting domain. About You – experience, education, skills, and accomplishments: It would be great if you also had . . . - Bachelor’s or master’s degree in pharmaceutical sciences - At least 5 years of relevant work experience in regulatory affairs or in supporting regulatory professional services/ Consulting projects. - Relevant experience in clinical trial data optimization, clinical data management, MAA submissions - Regulatory Intelligence – Pharmacovigilance, Clinical Trial, New and post approval registrations, etc. - Customer facing or customer service experience desirable. - Demonstrated ability to...