Clinical Trial Manager (Study Start Up CTM)
ICON · Taiwan
Skills in this posting
Extracted from the posting text by the instrument — the demand side, read literally.
The posting
Taiwan-FSP- Clinical Trial Manager (Study Start Up CTM)- Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Trial Manager at ICON , you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes. What You Will Do: You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:
Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
Build and manage strong relationships with trial investigators and stakeholders.
Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
Your Profile: You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. Required qualifications and experience:
University degree in medicine, science, or equivalent combination of education & experience
Demonstrated ability to drive the clinical deliverables of a study
Subject matter expertise in the designated therapeutic area
Proven ability to work efficiently to tight deadlines and manage multiple priorities.
Familiar with Study Start Up proccess
Nice to have country selection experience
Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:
Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here . Are you a current ICON Employee? Please click here to apply Originally posted on Himalayas
Excerpt from the original listing. The full, current text lives at the source. Read and apply there →
The PivotHop read
- What a clinical research coordinator actually earnsmedian, seniority, by country
- Alternative careers for a clinical research coordinatorevery measured route out
- All open clinical research coordinator rolesthe full board
Where these skills also reach
Adjacent occupations measured from the same postings — readiness is what a clinical research coordinator’s profile already covers.
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- 19 open statistician roles32% readiness from clinical research coordinator
- 4 open biomedical engineer roles20% readiness from clinical research coordinator
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