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Evidence Delivery Specialist
ICON Plc —Burlington, ON
Knowledge and understanding of the clinical study and drug development processes, GCP/ICH guidelines. Bachelor’s degree required preferably in medical or…
Trial Delivery Management (Advanced)
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Bachelor's degree in a relevant scientific discipline or healthcare-related field. You will have solid project and program management experience, with the…
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Evidence Delivery Specialist

ICON Plc
Burlington, ON

Apply Now

Job details

Full-time

Benefits

Childcare assistance
On-site childcare

Skills

Bachelor's
Communication skills

Full job description

Evidence Delivery Specialist

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

What you will be doing

Executes activities to fulfil sponsor oversight responsibilities and to maintain inspection-readiness, including
Maintain Study Inspection Readiness Tools
Coordinate and oversee periodic study-level TMF/Master File (MF) QC
Perform Periodic TMF/MF QC on behalf of Study/EAP Management
Customization of the study’s Expected Document List (EDL) in collaboration with the CROs
Collaborate with extended study team to develop, maintain, and execute activities according to the study Sponsor Oversight Plan
Ensure appropriate documentation of oversight and inspection-readiness tasks is maintained
Ensure handover documents are created, signed and filed in TMF
In collaboration with CRO, support creation, execution and maintenance of TMF/MF Plan
Supports key study start-up activities, in collaboration with CRO and internal functions as needed
Support compliance and quality deliverables
Create and maintain internal study/program trackers and systems as needed, including mailboxes and collaboration forums
Support budget management activities including

Your profile

Bachelor’s degree required preferably in medical or biological science or equivalent by experience
Knowledge and understanding of the clinical study and drug development processes, GCP/ICH guidelines
Excellent written and verbal communication skills as well as proven collaboration and influencing skills
Team oriented and flexible; ability to respond quickly to shifting demands and opportunities
Demonstrated ability to collaborate as well as work independently
Ability to effectively work with Clinical Research Organizations/External Providers
Preferred background in medical affairs/investigator initiated studies
Proven ability to interact widely and effectively within the company across regions, functions and culture
Ability to manage competing priorities

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, 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 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

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.

Apply Now

Refine Your Search

Evidence Delivery Specialist

Contract Specialist

Study Start Up Associate II

Clinical Research Associate

Trial Delivery Management (Advanced)

Evidence Project Manager

Manager, Investigator Site Budgets & Contracts

Sr CRA

Sr. Clinical Research Associate

Clinical Trial Transparency Anonymization Specialist

Country Study Operations Manager

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