Clinical Trial Manager - Regulatory - Ireland
2 days ago Be among the first 25 applicants
As a Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This will be focusign on Regulatory submissions, contract and budget negotiations and reviewing reports at site level. This is a local position within Ireland.
* Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA).
* Oversees and tracks clinical research-related payments. Payment reconciliation at study closeout.
* Oversees FCPA, DPS/OFAC, and maintenance of financial systems.
* Financial forecasting in conjunction with Sr. CTM /other roles.
* Executes and oversees clinical trial country submissions and approvals for assigned protocols.
* Develops local language materials including local language Informed Consents and translations.
* Interacts with IRB/IEC and Regulatory Authority for assigned protocols.
* Manages country deliverables, timelines and results for assigned protocols to meet country commitments.
* Responsible for quality and compliance in assigned protocols in country.
* Contributes to the development of local SOPs.
* Oversees CTCs as applicable.
* Coordinates and liaises with CRM, CTC, CRA, (Finance and Legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, CTRAs and local milestones.
* Collaborates closely with Headquarter to align country timelines for assigned protocols.
* Provide support and oversight to local vendors as applicable.
* Oversees and coordinates local processes, clinical and ancillary supplies management, importing and exporting requirements, supplies destruction, local electronic/hard copy filing, archiving and retention requirements, and insurance process management.
* Enters and updates country information in clinical and finance systems.
* Ownership of local regulatory and financial compliance.
* The position has a significant impact on how a country can deliver country-specific trial commitments and objectives especially during study start-up.
* Required to in/directly influence investigators, external partners and country operations and adheres to budget targets and agreed payment timelines.
* Works in partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas and externally with vendors and sites, IRB/IECs and Regulatory Authorities in submission and approval related interactions.
* Through continual interaction with local clinical team/s successfully delivers clinical and financial contracts within fair market value.
You Have
* Degree in the lifesciences is preferred
* Previous CRA experience is preferred
* Experience with negotiating at site level (contracts, budgets etc)
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, 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, colour, 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.
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Research, Analyst, and Information Technology
* Industries
Pharmaceutical Manufacturing
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