台湾 的 IQVIA 职位

Provides education to health care prescribers and their staff on the proper use of designated treatments for assigned disease area or reinforcement of study protocols as related to a clinical trial. · ...

Liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. · ...

Perform manage and coordinate activities for assigned opportunities/projects data mining and analysis formulate recommendations present to internal external stakeholders train support new team members/junior staff make recommendations process improvements. · ...

Design and deliver research studies independently with minimal support from project leader in an efficient manner. Deliver projects with total revenue at USD 300~500K per year as a key team member. · ...

This internship supports medical affairs solutions projects including data collection analysis and report writing. · Cases research data collection and analysis · Touring investigation materials analyses including interview minutesand extraction of insights · ...

Provides high quality timely development and on time input to client solutions for the pharmaceutical and related industries. · Under direct supervision assists with the review and analysis of client requirements or problems and the development of proposals of cost effective solu ...

This Analyst/Associate Consultant will provide high-quality development and input to solutions for service delivery. They will contribute to meeting client satisfaction objectives. · Supporting the design and build of new technology solutions including; understanding business nee ...

This is an accounting coordinator position at IQVIA. Assist daily financial work including payment documents arrangement. · ...

Provides administrative and/or technical support. · ...

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations. · ...

This role is an individual contributor assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the line manager (LM). The purpose of this role is to work together with global or regional Quality Management team(s), functional tea ...

The Associate Director Clinical Project Management will manage staff and provide guidance in accordance with organization's policies and applicable regulations. Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional devel ...

· ...

Job Overview · This role is an individual contributor assigned to designated Delivery Unit(s), sponsor(s), business line(s), and/or specific tasks as defined by the line manager (LM). · The purpose of this role is to work together with global or regional Quality Management team(s ...

Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs. · Bachelor's Degree Life sciences or related field Req · 7 years' relevant experience in a scientific or clinical environment inc ...

Associate Clinical Leads are an integral part of clinical trial delivery, working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. · ...

Admin Specialist performs various administrative tasks including document management and data entry. · ...

This position handles daily office administrative tasks and applies for departmental funds. · Maintains records of contracts and internal documents. · ...

We invite talented and motivated individuals to join us and grow with our organization as well the exciting field of RWE. · As part of the industry-leading global RWE solution, the IQVIA China Real-World Solution team is a young, energetic and fast-growing team consists of master ...

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, · Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements, · Work with sites t ...