About this role
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.
In this role you will be responsible for evaluating and optimizing the feasibility of clinical trials, ensuring they are well-planned and positioned for success.
What You Will Do:
You will lead on clinical research tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:
This is an oversight role and is responsible for the management of the Country and Site Feasibility Team as it relates to training, mentoring and performance.
Analyze results of country and site outreach and evidence to guide team members in building the recommended country and site strategy.
Evaluate performance of study deliverables against recommended countries and site performance to optimize future selection strategies.
Accountable for the delivery of the study specific Country and Site Feasibility strategy for each study in alignment with the trial objectives, sponsor's portfolio strategy
Responsible for the oversight of the Country and Site Feasibility Team, resourcing to each project, metrics related to the function and meeting the yearly objectives established in coordination with the SSU Head and senior leadership.CDA experience
Develop feasibility assessment questionnaire templates, input into survey tools, assess data and collate to develop meaningful metrics to drive recommendations and decisions on a global scale.
Maintain effective relationships with country teams, portfolio delivery teams and other business functions to support effective portfolio delivery.
Engage with study start up team to ensure site level feasibility is completed in line with study site selection strategy.
Trouble shoot any issues and resolve accordingly with input from the portfolio delivery teams.
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Your Profile:
You will have a strong foundation in clinical research, with the experience to work independently and guide others.
Required qualifications and experience:
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Minimum of 4 years country and site feasibility experience for global trials
Leadership skills and ability to effectively collaborate with colleagues in Clinical Operations and cross-functionally to deliver on portfolio deliverables and objectives
Must have extensive expertise in strong knowledge of ICH/ GCP guidelines and multinational clinical trial regulations
Must have experience working across multiple phases of development and in multiple therapeutic areas
Strong organizational and project management skills, with experience in handling multiple feasibility projects simultaneously.
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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
About ICON plc
Global contract research organization providing outsourced clinical development services. Headquartered in Dublin, Ireland.