Parexel

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 Consultant – Regulatory Labeling Strategist sought by Parexel Consulting to lead global labeling strategy for biopharma clients. This remote role requires 5-7 years’ industry experience, including 2+ years in global labeling with strategic leadership. You will drive CCDS...

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...

Parexel seeks a remote **Data Management Lead** (Data Manager II) based in the Continental US. You will oversee study data delivery timelines, including Go-Live and Final Database Lock, while collaborating with global cross-functional teams. This role demands 6+ years of clinical research experie...

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...

Senior Clinical Research Associate / CRA II – Oncology. Join Parexel to drive global clinical trials with 60-80% travel across the US. Leverage 3+ years of site monitoring experience (2+ in Oncology preferred) and deep ICH/GCP knowledge. Ensure patient safety, manage investigator sites, and enjoy...