- TaipeiPermanent
The Clinical Research Associate will need to monitoring assigned clinical trials and as the primary contact to deal with request from sites.
Top 10 Global Pharmaceutical Company.
Global level studies.
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The Clinical Research Manager will lead a team to conduct clinical studies management. This role is responsible for assigned local clinical projects and ensuring the good quality results.
People management opportunity.
Sponsor side opening.
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The Clinical Project Manager will handle clinical projects and collaborate with venders. Internally, this role will co-work with cross-functional teams to do clinical projects with his/her solid experience and strong communication skills.
Clinical project management role.
Sponsor hired opportunity.
Save Job View Job - InternationalPermanent
The Scientific Manager will be responsible for early stage clinical development and project management tasks. This role will collaborate with the HQ closely.
Promising product pipeline
New set up team with flexible and proactive culture
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The clinical project manager is responsible for handling projects in oncology. And this role needs to mentor CRAs, financial budget management and project timeline management.
Regional to global level projects.
Work-life balance opportunity.
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This role is responsible for ensuring implementation of Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GPvP) oversight. Also, this role needs to ensure the collaboration and partnership with cross-functional teams meet a high level of compliance.
Develop professional skills
Positive company culture
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The Clinical Research Associate(Senior CRA/ CRAII) will be based in Taipei, completed project activities associated with monitoring functions of global level clinical research studies with my client's new sponsors while continuing to develop a solid understanding of the drug development process.
Global studies and clinical trials.
New created headcounts.
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The manager, site start-up will be responsible for coordinating with major functional area leads to identify and evaluate fundamental issues pertaining to Site Start-Up, project regulatory process, patients enrolment, interpret data on complex issues and providing professional solutions.
Strong product pipeline in oncology area.
Project management opportunity.
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