Jobs: parexel

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.   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...

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...

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...

Data Management Lead llThe Data Management Lead ll provides leadership and expertise in all aspects of Data Management. Develop and manage timelines for study data deliveries, including Go-Live, Interim Deliveries, and Final DB Lock. Collaboration with the relevant functions (Clinical, Biostatistics, Database Programming, Medical, Medical Writing etc.)...

When our values align, there's no limit to what we can achieve.   Data Management Lead ll The Data Management Lead ll provides leadership and expertise in all aspects of Data Management. Develop and manage timelines for study data deliveries, including Go-Live, Interim Deliveries, and Final DB Lock. Collaboration with the relevant functions...

When our values align, there's no limit to what we can achieve.   Data Management Lead ll The Data Management Lead ll provides leadership and expertise in all aspects of Data Management. Develop and manage timelines for study data deliveries, including Go-Live, Interim Deliveries, and Final DB Lock. Collaboration with the relevant functions...

As a member of Parexel’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and Parexel teams in differing locations. Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and...

Develop knowledge of SAS and processes/procedures within other Parexel functional areas Develop knowledge of clinical trial process Check own work in an ongoing way to ensure first-time quality Work on dummy datasets, tables, listings and figures Work on some new statistical methods used in clinical trials Ensure compliance with SOPs/Guidelines, ICH-GCP, and...

Job Purpose:The primary role of the Senior Software Engineer is to Designs (HL,LL), modifies, develops, writes and implements software programming applications to satisfy complex requirements, to time and budget. She/he defines the technical requirements and creates high-level specifications ensuring feasibility, functionality and integration with existing...

When our values align, there's no limit to what we can achieve.   Senior Director, Medical Writing Services . Job Purpose: The primary role of the Senior Director is to ensure the satisfactory management of Medical Writing Services (MWS) operations in the assigned region in a manner consistent with Corporate and Department mission and goals....

When our values align, there's no limit to what we can achieve.   Senior Director, Medical Writing Services . Job Purpose: The primary role of the Senior Director is to ensure the satisfactory management of Medical Writing Services (MWS) operations in the assigned region in a manner consistent with Corporate and Department mission and goals. In...

Senior Director, Medical Writing Services.Job Purpose: The primary role of the Senior Director is to ensure the satisfactory management ofMedical Writing Services (MWS) operations in the assigned region in a manner consistent with Corporateand Department mission and goals. In addition, the Senior Director understands stakeholder needs,preferences,...

When our values align, there's no limit to what we can achieve.   Parexel’s Strategic CGMP Compliance team is known for our unparalleled breadth and depth of expertise globally. Parexel CGMP Compliance offers services which create and maximize product value for clients throughout the product lifecycle, leveraging our unique fusion of scientific,...

When our values align, there's no limit to what we can achieve.   Clinical Trial Protocol Specialist The Clinical Trial Protocol Specialist will research, create, and edit clinical trial protocols as well as provide expert support for protocol development. Operates as a lead medical writer or as a Subject Matter Expert (SME) to support Medical Writers...

When our values align, there's no limit to what we can achieve.   Clinical Trial Protocol Specialist The Clinical Trial Protocol Specialist will research, create, and edit clinical trial protocols as well as provide expert support for protocol development. Operates as a lead medical writer or as a Subject Matter Expert (SME) to support Medical...

India, Remote **Job ID** R0000017927 **Category** Clinical Trials **ABOUT THIS ROLE**: **TMF Support** - Collaborates with the TMF Inspection Readiness Specialist to plan and execute assigned tasks. - Maintains overview of the agreed planning, proactively providing status updates and notifying trends to the study team and TMF IR Specialist. - Stays...