Study Delivery Lead NIS

Study Delivery Lead NIS

About the role

An exciting role for a Clinical Trial Manager with experience in leading and driving cross-functional teams

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes. In this role, your focus will be NIS Non-Interventional Studies.

What You Will Do:

Ideally, you will be a Clinical Trial Manager with retrospective and prospective designs, post authorization safety studies, real world evidence, and epidemiology experience. This is a leadership role and the CTM will bring experience in leading and driving cross-functional teams.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team. This position combines end-to-end design, execution, and reporting of clinical studies and trials including:

• Non-interventional studies using primary data collection, including prospective studies enrolling patients and / or HCPs, de novo registries, discrete choice experiments, creation of new datasets with secondary data (e.g. with EMRs / chart abstraction), patient reported outcomes development and validation.

• Non-interventional comparative and descriptive studies using secondary data sources, including retrospective studies, burden of illness and drug utilisation studies, prevalence / incidence studies of exposure, risk factors and outcomes.

• Studies utilizing a mixture of existing medical data and the collection of new data via sites or directly via patients.

• Economic modelling studies and supplemental analyses of clinical trials / meta-analyses.

• Interventional and low-interventional studies.

Required qualifications and experience:

• A minimum ideally of 4+ years of experience in a Clinical Trial Management position at a CRO or Pharmaceutical Organization.

• Bachelor's degree in health, life sciences, or Advanced degree (e.g. MS, PhD, PharmD)

• At least 10+ years ideally of relevant experience in clinical trial management.

• Experience in managing complex or global trials is advantageous.

• Preferred: Experience in managing all trial components from start-up to database lock.

• Preferred: Experience in leading and driving cross-functional teams including oversight of external CROs, etc.

• Proven expertise in the proactive identification of issues which may impact clinical programmes coupled with the ability to contribute to solutions affecting cross-functional matrix teams.

• Demonstrated experience leading in matrix environment to deliver projects, develop clinical plans, and manage change.

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 maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

At ICON, inclusion & belonging are fundamental to our culture and values. 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 or submit a request here

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.

Are you a current ICON Employee? Please click here to apply

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Location

Sofia, Warsaw, Bucharest, Madrid, London

Reference: JR163100

Remote Working

Remote

Job Categories

Clinical Trial Management

Description

• About the Role Our client is seeking a talented Global Study Manager to support the delivery of Cell Therapy global clinical studies from protocol development through study close-out and archiving. Wo

• What is the difference between a clinical trial manager and a clinical project manager?

• Global Study Manager

Salary

Location

UK, Reading

Location

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Trial Management

Job Type

Permanent

Description

• About the Role Our client is seeking a talented Global Study Manager to support the delivery of Cell Therapy global clinical studies from protocol development through study close-out and archiving. Wo

• Reference

• JR162238

• Expiry date

• 01/01/0001

• Author

• Dominic Brady

• Read more

• Shortlist Save this role