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Project Manager

  1. Taiwan
2024-109628
  1. Project Management
  2. ICON Strategic Solutions
  3. Remote

About the role

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ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

 

As a Project Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.


What you will be doing:

Overview

As a regional project manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

  • Clinical Trial Management and Central Trial Oversight services provide for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials.
  • May act as the lead over a team of CTMs across a project/program, on insourced and outsourced studies.
  • Able to lead taskforces and provide innovative input.

 

What you will be doing:

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance. We are hiring a "Regional project manager" to work closely with our client, a leading pharmaceutical company.

Overview

Our Clinical Trial Management and Central Trial Oversight services entail coordinating global and regional clinical trial activities for both in-house and outsourced trials. The focus is on leading the Study Management Team (SMT) to ensure timely progression of clinical operations across various stages: country & site feasibility, selection, setup, execution, closure, and vendor activities. These responsibilities are assigned by the Global Clinical Development Operations Trial Leader (GTL).

 

The role also involves assisting the GTL in overseeing CRO, country, and site tasks. This includes managing global vendors engaged in site-related activities like IVRS, Central Lab, ePRO, Imaging, Translation, Printing, Ancillary supplies, and Meeting Planners. Engaging with stakeholders within and outside Global Clinical Development Operations (GCDO) is a key aspect, including collaboration with Study Responsible Physicians, Global Data Managers, Trial Supply Managers, CRO and vendor personnel, as well as trial sites if applicable.

 

Key Responsibilities:

  • Collaborate closely with the GCDO Trial Leader (GTL) as a vital Trial Team member.
  • Ensure compliance with protocol, company SOPs, GCP codes, regulations, and guidelines from start to finish, maintaining inspection readiness.
  • Assume ownership of assigned tasks and demonstrate the ability to step in for the GCDO Trial Leader when needed.
  • Handle more intricate assignments that can significantly impact business outcomes.
  • Lead a team of CTMs across projects/programs, both insourced and outsourced studies.
  • Provide innovative input and lead taskforces, contributing to process enhancements and non-project initiatives.
  • If you're ready to influence the pharmaceutical landscape and work alongside industry leaders, apply now for the role of Global Clinical Trial Manager. Make a difference while advancing your career in a dynamic and impactful setting.

 

 

#LI-remote

#LI-ST1


You are:

  • Minimum 3 years' clinical trial management in pharma/CRO. And cover more than 3 countries. 
  • Proficient in ICH-GCP, local regulations.
  • Strong clinical research operations expertise.
  • Successful end-to-end trial management track record.
  • Proven leadership driving Study Management Teams.
  • Skilled in delegation and stakeholder management.
  • Forming and leading high-performing teams.
  • Coordinating global virtual teams 2-3 years.
  • Proactive planning, risk management, consensus building.
  • Strong project management, IT, decision-making.
  • Solution-focused, risk mitigation.
  • Fluent in English and local language.
  • Effective communication and presentation skills.
  • Budget oversight capability.

 


What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others



Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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