parexel

Parexel is seeking a Patient Safety Specialist to support global pharmacovigilance activities across clinical trials and post‑market projects. You will help implement safety processes, assist with regulatory submissions, and collaborate with cross‑functional teams to ensure quality and compliance. The role covers ICSR processing, literature surveillance,...

Parexel Consulting is seeking an Associate to support qualitative research and client deliverables. You’ll work under the Project Lead to ensure timely, high-quality outputs and maintain effective client relationships in a collaborative, cross-cultural team. Ideal candidates have a Bachelor's or Master's in a relevant field, 1–2 years of qualitative...

Parexel is seeking a Technical Consultant to join our Regulatory Operations team. This remote role supports global regulatory activities from Mexico and partners with internal teams, software vendors, and clients to provide technical expertise in publishing systems and eCTD submissions. You will configure, validate, and maintain regulatory technology...

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 Philippines in Manila is seeking a part-time Intern to contribute to clinical trial support and site management with emphasis on quality and compliance.You will assist with ISF preparation, TMF uploads, document scanning, and coordination of forms and shipments, while learning regulatory practices.Strong MS Office skills and English communication are...

Join Parexel as a part-time Intern in Manila, contributing to clinical trial support and site management with a focus on quality and compliance.Your RoleKey responsibilities include:Assist with site activation tasks such as building Investigator Site Files (ISF), customizing study-specific forms and templates, coordinating local printing, and supporting...

Parexel FSP is seeking a Global Study Manager II to lead the study management lifecycle across multiple regions. You will oversee CRO relationships, vendor deliverables, and study budgets, driving timelines and data quality.The role requires strategic input and hands-on execution across study startup, monitoring, and closure. Ideal candidates will bring...

Technical Consultant, Regulatory Operations (eCTD Publishing & Regulatory Systems) - Remote Location: Mexico (Candidates located in other countries cannot be considered) Work Schedule 11:00 AM to 8:00 PM (Mexico Time) This schedule is mandatory due to collaboration with global teams and stakeholders. Ideal candidates currently hold titles such as...

Parexel FSP is looking for Global Study Manager II in Argentina, Brazil or Mexico! Job Summary The Global Study Manager II (GSM II) provides operational leadership throughout the study lifecycle, with accountability for oversight and execution of study management, site management, preferred Contract Research Organization (pCRO), and vendor deliverables for...

Key Accountabilities Maintain expert-level knowledge of safety profiles, labeling, and global regulations Lead development of project-specific procedures and workflows Provide technical guidance to junior team members Prepare for and participate in audits and inspections Analyze metrics and drive continuous improvement Collaborate with...

The Patient Safety Specialist supports global pharmacovigilance activities across clinical trials and post-marketed projects, contributing to the execution of safety processes with increasing autonomy and expertise. Responsibilities may include case processing management, regulatory submissions or support, literature surveillance, affiliate coordination, and...

A leading global biopharmaceutical services firm is seeking a Regulatory Affairs Specialist in Manila. This role requires expert knowledge of drug safety regulations and the ability to provide technical guidance. Responsibilities include managing regulatory applications and submissions, ensuring compliance with global standards, and collaborating with...

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...

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...

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...

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...

Join Parexel as a part-time Intern in Manila, contributing to clinical trial support and site management with a focus on quality and compliance. Your Role Key responsibilities include: Assist with site activation tasks such as building Investigator Site Files (ISF), customizing study-specific forms and templates, coordinating local printing, and...

Parexel International is seeking a Patient Safety Specialist to support global pharmacovigilance activities across clinical trials and post-marketed projects. You will contribute to safety processes with growing autonomy, handling ICSR processing, safety submissions, literature surveillance, and cross-functional coordination with clients. The role requires...

The Patient Safety Specialist supports global pharmacovigilance activities across clinical trials and post-marketed projects, contributing to the execution of safety processes with increasing autonomy and expertise. Responsibilities may include case processing management, regulatory submissions or support, literature surveillance, affiliate coordination, and...