parexel

Parexel is seeking a Senior Regulatory Associate to author global CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs. You will prepare CMC packages, support GMP submissions, manage change control assessments, and ensure regulatory compliance across regions.Ideal candidates have at least 5 years in biotech/pharma regulatory...

Parexel International is seeking a Technical Consultant to join our Regulatory Operations team. You will serve as a subject matter expert for regulatory publishing systems, document management technologies, and electronic submission tools used to support global regulatory activities.This remote role partners with internal teams, software vendors, and clients...

Parexel is seeking a Senior Regulatory Associate to author global CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs. You will prepare CMC packages, support GMP submissions, manage change control assessments, and ensure regulatory compliance across regions.Ideal candidates have at least 5 years in biotech/pharma regulatory...

When our values align, there's no limit to what we can achieve.At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at...

Parexel, a global clinical research partner, seeks a Regulatory Affairs Sr. Associate focused on LATAM COFEPRIS interactions to support product lifecycle management.You will drive regulatory strategy, oversee submissions, labeling reviews, and post‑approval changes, collaborating with global and regional teams to ensure timely, compliant approvals.The role...

Parexel is seeking a Senior Regulatory Associate to author global CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs. You will prepare CMC packages, support GMP submissions, manage change control assessments, and ensure regulatory compliance across regions.Ideal candidates have at least 5 years in biotech/pharma regulatory...

Parexel is hiring a Senior Clinical Data Manager in Mexico or Argentina to lead data management activities across global projects and to participate as a key member of a multi-disciplinary team planning, leading and executing DM tasks for phase 1–4 studies.You will ensure data quality, coordinate with CROs, design eCRFs, develop data management plans, and...

Parexel is hiring a Participant Recruitment Site Engagement Associate in Mexico. The role supports clinical trial site staff to help access client systems, track recruitment progress, and ensure timely updates and escalations in line with client standards.You will oversee site information, coordinate tasks, and contribute to study-level recruitment planning....

Parexel, a global clinical research partner, seeks a Regulatory Affairs Sr. Associate focused on LATAM COFEPRIS interactions to support product lifecycle management.You will drive regulatory strategy, oversee submissions, labeling reviews, and post‑approval changes, collaborating with global and regional teams to ensure timely, compliant approvals.The role...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at...

Parexel is seeking a Global Trade Compliance Specialist to join our Clinical Logistics team. You will manage import and export operations across Latin American countries, ensuring customs compliance and supporting clinical research projects.Ideal candidates have strong knowledge of international trade in healthcare, experience coordinating with customs...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at...

Parexel is seeking a Consultant of Regulatory Strategy for Mexico with in-office requirements. You will manage regulatory dossiers, guide submissions, and act as a primary liaison with LATAM health authorities.The role supports infectious diseases programs across Latin America within a global regulatory team. The ideal candidate brings 5+ years in pharma...

When our values align, there's no limit to what we can achieve.At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at...

Parexel is seeking a Global Trade Compliance Specialist to join our Clinical Logistics team. You will manage import and export operations across Latin American countries, ensuring customs compliance and supporting clinical research projects.Ideal candidates have strong knowledge of international trade in healthcare, experience coordinating with customs...

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at...

Parexel FSP is hiring a Participant Recruitment Site Engagement Associate in Mexico Provides recruitment and engagement support to clinical trial site staff to help facilitate access to client systems, ensure timely updates about recruitment of participants, communicate recruitment plans and escalations appropriately in a manner that is consistent with...

Technical Consultant, Regulatory Publishing (eCTD Publishing & Regulatory Systems) - Remote Primary Location: Mexico Secondary locations: Colombia, Chile, Perú Work Schedule 11:00 AM to 8:00 PM (Mexico Time) This schedule is mandatory due to collaboration with global teams and stakeholders. About the Role Parexel is seeking a Technical Consultant to join...

Technical Consultant, Regulatory Publishing (eCTD Publishing & Regulatory Systems) - Remote Primary Location: Mexico Secondary locations: Colombia, Chile, Perú Work Schedule 11:00 AM to 8:00 PM (Mexico Time) This schedule is mandatory due to collaboration with global teams and stakeholders. About the Role Parexel is seeking a Technical Consultant to join...

Join Our Growing Team of CMC Regulatory Professionals!The Senior Regulatory Associate will author global CMC variation submissions, annual reports, renewals, and post-approval MAA roll-outs, including responses to Health Authority requests. Responsibilities include preparing and reviewing CMC packages, supporting GMP submissions, managing change control...