Parexel - India

Senior Regulatory Affairs Consultant sought in India to lead global submissions for biological products including vaccines, monoclonal antibodies, and plasma-derived therapies. Requires expertise in MAAs, variations, and renewals across US, EU, Japan, Canada, Switzerland, and Australia. Ideal can...

Regulatory Affairs Consultant sought for a role based in India. You will leverage 8-11 years of experience in EU & US regulatory procedures to manage global submissions and lifecycle maintenance. Key responsibilities include preparing submission packages (Modules 1-5), handling Health Authority q...

Senior Regulatory Affairs Associate specializing in Clinical Trial Applications. Lead global CTA submissions under EU CTR and ROW, managing complex regulatory projects for biopharma clients. Requires 5+ years in pharma/CRO with strong project management skills. Enjoy flexible remote work from Ind...

Senior Regulatory Affairs Associate sought for a remote role in India with Parexel Consulting. Leverage 5-8 years of EU & US regulatory expertise to develop global submission strategies and manage lifecycle maintenance. Drive post-approval changes, Health Authority queries, and compliance readine...

Join us as a Site Care Partner in Mumbai, India, to drive clinical trial success. Leverage your GCP/ICH expertise to manage site start-up, activation, and investigator relationships. We seek strong communicators with cross-functional skills and adaptability to new technologies. Enjoy flexible wor...

MLR Vault Technician role in India seeks a detail-oriented professional to manage content within Veeva Vault PromoMats and Medical. Key duties include creating placeholders, uploading versions, and reference linking in a cross-functional environment. Ideal candidates have a scientific background ...

Join Parexel Consulting as a Health Economics Consultant (Evidence Evaluation) in Remote India. Leverage your HEOR and SLR expertise to deliver high-quality, strategic solutions for biopharma clients. Requires a Master’s/PhD in Life Sciences, 5+ years in evidence evaluation, and strong analytical...

Join Parexel as a Site Visit Report Reviewer (SVRR) in India. You will ensure clinical visit reports meet GCP, SOP, and regulatory standards while collaborating with CRAs and project teams. Monitor open issues, protocol deviations, and SAEs to closure. Ideal for detail-oriented professionals with...