中国 的 Parexel 职位

Provides clinical and scientific expertise to the clinical trial strategy and protocol development process. · ...

We improve the world's health. · We take our work personally, we do it with empathy and we're committed to making a difference. · ...

· We all share the same goal - to improve the world's health. · To achieve this goal, we need individuals who are passionate about improving people’s lives through their work in clinical development. · Job requirements: · ,""," ...

Develop and execute account strategies for assigned clients and territories. Build and maintain relationships with senior decision-makers and key stakeholders. · ...

The Clinical Trial Assistant is responsible for performing a variety of research, database, and clerical duties in support of multiple clinical trials. · ...

We all share the same goal - to improve the world's health. · Comply with required training curriculum.Complete timesheets accurately as required.Submit expense reports as required. Maintain a working knowledge of and comply with Parexel processes, ICH-GCPs and other applicable r ...

Maintain overall integrity of study implementation at clinical sites act as direct contact between PAREXEL assigned sites assess evaluate problem solve resolve site issues build relationships investigators site staff facilitate support access relevant study systems ensure complia ...

At Parexel we all share the same goal - to improve the world's health. · Act as PAREXEL's direct contact with assigned sites. · ...

As a Senior Clinical Project Manager at Parexel, you will oversee study start-up activities, provide inputs to project tools and study plans, and develop site selection and monitoring plans. You will also lead a virtual team across locations and cultures, negotiate with diplomacy ...

The clinical research associate II will act as Parexel's direct point of contact with assigned sites, · building relationships with investigators and site staff.Conduct remote qualification visits (QVs), · generate visit/contact reports, · determine appropriate follow-up action, ...

Contribute to the development of a therapy that ultimately will benefit a patient. · PhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experience · ...

+Improve the world's health from clinical trials to regulatory, consulting and market access. · Study design expertise for IIT and RWE studies · Protocol development experience · ...

Implements and monitors clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH GCP guidelines. · ...

+The Clinical Research Associate II will be responsible for maintaining overall integrity of study implementation and adherence to study protocol at clinical sites. · +Act as PAREXEL's direct contact with assigned sites. · Evaluate if on-site staff assignment is still accurate an ...

Maintenance (from initiation through close out): Ensure timely and accurate completion of project goals and update of applicable trial management systems. Work with team members to meet project goals, provide strategy for efficient project planning and goal completion, and encour ...

This is a site-facing position responsible for implementing client's Site and Monitoring Health strategy in alignment with ICH GCP E6 and E8. · ...

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

This position of senior biostatistician requires study design expertise, specifically for IIT and RWE studies. The ideal candidate will have protocol development experience and proficiency in SAS and R programming. · ...

The Clinical Trial Administrator (CTA) performs research, database, and clerical duties in support of multiple clinical trials. · This position also provides administrative support by reviewing vendor invoices, · tracking payments, taking meeting minutes during project team meeti ...

When our values align, there's no limit to what we can achieve. · ...