台湾 的 Parexel 职位

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. · ...

The Clinical Research Associate I/II/Senior will work on clinical trials to improve patients' health. · They will collaborate with investigators and site staff to ensure timely completion of project goals. · ...

+Job summary · At Parexel, we all share the same goal - to improve the world's health. · +Bachelor's degree in information technology, Computer Science, or a related field. · Minimum of 1-3 years of experience in IT support. · +Work on the IT tickets raised by business related to ...

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

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. · ...

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. · Exercise sound judgment i ...

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. · ...

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

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. · ...

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... · ...

Supports the accounts payable function by performing tasks such as vendor invoice processing and quality checking. · ...

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 ...

+ Project Management: Ability to fill Statistical Programming Lead role on projects. Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to. · Coordinate and lead a statistical programming team to successful completion of a study within g ...

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

At Parexel, we all share the same goal - to improve the world's health. · ...

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 ...

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

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. · Project Execution: Responsible for product and GMP registration dossier preparation and submission of as ...