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Company:
ICON
Posted: April 29, 2025
As a Clinical Registry Coordinator, you will join the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
What you will be doing :
1.
Provide clinical registry support, oversight, and accountability for one or more development programs for clinical trials.
2.
Lead with the clinical development team and other partners to establish and confirm clinical registry expectations for assigned trials.
3.
Develop and deliver the Disclosure Plan with the CDTL and Patent attorney.
4.
Gather content and integration requirements for registration records with CDT and other partners.
5.
Set timelines and follow up regularly to ensure delivery of disclosure milestones.
6.
Submit approved documents to registries worldwide, either directly or through local staff.
7.
Track, report, and document disclosure records and related documents in relevant tools and systems.
8.
Assist partners and local teams in maintaining accurate source data related to disclosures.
9.
Ensure timely resolution of planning issues for compliant delivery.
10.
Participate in working groups to meet trial needs and deliverables.
11.
Identify and share lessons learned, best practices, and FAQs.
12.
Present and train at business partner meetings.
13.
Collaborate with other CRCs and managers for alignment and information sharing.
You are :
• Minimum 4 years of relevant experience in a clinical development environment.
• Bachelor's degree in Health or Science with experience in clinical research roles.
• Clinical Registry experience is preferred.
• Experience with clinical trial or regulatory document management is preferred.
• Experience working in diverse, cross-functional, global teams.
• Advanced skills in Microsoft Office, including data analysis.
What ICON can offer you :
We prioritize building a diverse culture that rewards high performance and nurtures talent.
Our benefits include competitive salary, various leave entitlements, health insurance, retirement plans, and well-being programs.
We support an inclusive environment and are committed to equal opportunity employment.
We encourage all qualified candidates to apply, even if they do not meet every requirement.
•
What you will be doing :
1.
Provide clinical registry support, oversight, and accountability for one or more development programs for clinical trials.
2.
Lead with the clinical development team and other partners to establish and confirm clinical registry expectations for assigned trials.
3.
Develop and deliver the Disclosure Plan with the CDTL and Patent attorney.
4.
Gather content and integration requirements for registration records with CDT and other partners.
5.
Set timelines and follow up regularly to ensure delivery of disclosure milestones.
6.
Submit approved documents to registries worldwide, either directly or through local staff.
7.
Track, report, and document disclosure records and related documents in relevant tools and systems.
8.
Assist partners and local teams in maintaining accurate source data related to disclosures.
9.
Ensure timely resolution of planning issues for compliant delivery.
10.
Participate in working groups to meet trial needs and deliverables.
11.
Identify and share lessons learned, best practices, and FAQs.
12.
Present and train at business partner meetings.
13.
Collaborate with other CRCs and managers for alignment and information sharing.
You are :
• Minimum 4 years of relevant experience in a clinical development environment.
• Bachelor's degree in Health or Science with experience in clinical research roles.
• Clinical Registry experience is preferred.
• Experience with clinical trial or regulatory document management is preferred.
• Experience working in diverse, cross-functional, global teams.
• Advanced skills in Microsoft Office, including data analysis.
What ICON can offer you :
We prioritize building a diverse culture that rewards high performance and nurtures talent.
Our benefits include competitive salary, various leave entitlements, health insurance, retirement plans, and well-being programs.
We support an inclusive environment and are committed to equal opportunity employment.
We encourage all qualified candidates to apply, even if they do not meet every requirement.
•
Read the full job description and apply online on the recuiter's web-site
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