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Cta Submission Manager (Ivd)

4-7 years
Not Disclosed
10 June 5, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

CTA Submission Manager (In Vitro Diagnostic Regulations - IVDR)

Location:

Remote – Any EMEA Location (including Czech Republic, Hungary, Poland, Romania, UK)

Job ID:

2025-119367

Department:

Regulatory Affairs – ICON Strategic Solutions

Managed By:

Patrick Hale
(Recruiter – Reachable via ICON careers site)


About ICON:

ICON plc is a global healthcare intelligence and clinical research organization. With a focus on innovation, quality, and inclusivity, ICON leads advancements in regulatory and clinical development worldwide.


Role Overview:

As a CTA Submission Manager (focused on IVDR), you will oversee and execute clinical trial application (CTA) submission strategies across global and regional studies. This includes coordination with cross-functional teams and ensuring timely, compliant submission of IVD-related documentation in line with industry and regulatory standards.


Key Responsibilities:

  • Lead operational submission strategy and activities for assigned CTAs and IVDR submissions.

  • Serve as Subject Matter Expert (SME) for CTA/IVDR submissions.

  • Collaborate with study teams to prepare, review, and manage submission documentation.

  • Author and coordinate Annex I and other key documents.

  • Support submission to Health Authorities (HA) and Ethics Committees (EC).

  • Coordinate translations and manage the submission build process.

  • Monitor and respond to RFIs (Requests for Information) via CTIS and internal systems.

  • May act as IVD applicant or local country liaison as needed.

  • Escalate and resolve submission issues proactively.


Candidate Profile:

  • Bachelor’s degree in Pharmacy, Life Sciences, Business, or IT (or equivalent experience).

  • Strong knowledge of CTA and Ethics Committee processes globally.

  • Demonstrated experience with IVDR submissions.

  • Technical proficiency and adaptability to regulatory software and standards.

  • Excellent communication, organizational, and project management skills.


Benefits at ICON Include:

  • Competitive salary and benefits

  • Remote work flexibility

  • Comprehensive health and insurance options

  • Retirement planning tools

  • Employee Assistance Programme (LifeWorks)

  • Work-life balance and wellness initiatives


Diversity & Inclusion Statement:

ICON supports an inclusive, respectful, and accessible work environment. Candidates of all backgrounds are encouraged to apply. Reasonable accommodations are available upon request.


Application Note:

Even if you don’t meet every qualification, you are encouraged to apply. ICON values diverse experience and perspectives.