Parexel - India, IT - Administration, Remote work

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...

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 ...

Senior Physician, Patient Safety role in India seeks an MBBS/MD with 2+ years of ICSR medical review experience. You will ensure global drug safety compliance, manage adverse event reporting, and serve as a Subject Matter Expert. Ideal for pharmacovigilance professionals with strong medical termi...

Senior Medical Writer, Patient Safety role in Bengaluru, India. Lead the preparation of complex aggregate safety reports (PSURs, PBRERs, DSURs) and drive strategic safety submissions. Requires expertise in pharmacovigilance regulations and signal detection. Join a team focused on global complianc...

Senior Regulatory Affairs Associate sought for Parexel Consulting to lead radiopharmaceutical lifecycle management. Leverage expertise in CMC authoring, safety labelling, and Health Authority submissions. This remote role based in India offers flexible work, global client exposure, and mentorship...