Parexel 职位 台湾

We all share the same goal - to improve the world's health. · Work on IT tickets raised by business related to applications. · Understand business functionality of applications supported. · ...

This role involves working as a Clinical Research Associate (CRA) for Hematologic Oncology studies. · Maintenance (from initiation through close out):Act as Parexel's direct contact with assigned sites. · Build relationships with investigators and site staff. · ...

At Parexel, we all share the same goal - to improve the world's health. · Act as Parexel's direct point of contact with assigned sites · Buid relationships with investigators and site staff · ...

We are looking for a Senior Clinical Research Associate to join our team at Parexel. As a Senior Clinical Research Associate, you will be responsible for ensuring the overall integrity of study implementation and adherence to study protocol at clinical sites. · ...

We all share the same goal - to improve the world's health. · Negotiate directly with clinical trial sites on cost, business, and contractual terms, · Lead study-level site contracting activities, · guide other contract leads, · and serve as the primary contact for site contracti ...

The Senior Regulatory Affairs Associate will act as primary RA representative for local Commercial and medical team, assess and mitigate impact of changes with local team, and support post-approval regulatory activities.Key responsibilities include prioritizing work to achieve sp ...

At Parexel, we all share the same goal - to improve the world's health. · Good analytical skills · Prior experience with SAS programming required · ...

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. · ...

Act as PAREXEL's direct contact with assigned sites. · Build relationships with investigators and site staff.Facilitate and support site with access to relevant study systems. · ...

This role involves providing technical support to clinical business users, troubleshooting and resolving issues related to applications, and collaborating with other IT team members. · ...

Parexel is seeking a Senior Clinical Research Associate to join their team. As a key member of the clinical development solutions group, this role will be responsible for ensuring timely and accurate completion of project goals and updating applicable trial management systems. · ...

The Clinical Study Administrator will contribute to site activation by assisting with staff access to vendor systems and following up on training completion. · Project Initiation & Planning: Contribute to site activation and project management. · Project maintenance  · ...

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access... · ...

This position involves production and/or QC of derived datasets statistical outputs using programming techniques coordination of project teams client interactions analysis planning report writing training in statistical analysis participation in process/quality improvement initia ...

Senior Statistical Programmer is responsible for project management, statistical programming, and training. They must have excellent analytical skills, proficiency in SAS, and knowledge of SOPs/Guidelines. · ...

Assist with the development of statistical analysis plans, mock shells, and programming specifications. Under supervision, performing data review and statistical analysis. · ...

Job summary · Improve the world's health by contributing to the development of a therapy that ultimately will benefit a patient. · ...

The Clinical Research Associate (CRA) will be responsible for ensuring timely and accurate completion of project goals and update of applicable trial management systems. · ...

+At Parexel, we all share the same goal - to improve the world's health. · +Coordinate project start-up activities, · creation of global programs, · tracking spreadsheets, · and other required documentation. · Review statistical analysis plans · and mock-shells. · ...

The successful candidate will lead study-level site contracting activities, guide other contract leads, and serve as the primary contact for site contracting issues and timelines on assigned studies. · ...