Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Ecoa Lead - East Coast

Icon
ICON
8+ years
Not Disclosed
10 July 21, 2025
Job Description
Job Type: Full Time 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

 

eCOA Lead – Clinical Trials | Remote (East Coast USA)

ICON Strategic Solutions is seeking an experienced eCOA Lead to oversee and optimize the end-to-end electronic Clinical Outcome Assessment (eCOA) processes across global clinical trial programs. This remote-based opportunity is ideal for professionals with deep experience in clinical data systems, regulatory compliance, and vendor oversight within the pharmaceutical or biotech industry.

Key Responsibilities:

  • Lead development and governance of eCOA frameworks across global clinical programs

  • Serve as eCOA SME, guiding cross-functional teams through end-to-end implementation

  • Develop KPIs, performance metrics, and conduct vendor oversight meetings

  • Standardize global eCOA operations for compliance and efficiency

  • Create eCOA documentation and training programs to ensure audit-readiness

  • Drive patient and site engagement with structured journey mapping and educational initiatives

  • Monitor industry trends and ensure continuous regulatory inspection readiness

  • Maintain centralized eCOA portals and knowledge-sharing systems

  • Manage vendor compliance including copyrights, translations, and licensing

Required Skills & Qualifications:

  • Bachelor’s or Master’s degree in Life Sciences or related field

  • Minimum 8 years of clinical trial experience, including direct eCOA implementation

  • Strong knowledge of ICH-GCP, FDA, and EMA regulations

  • Proven expertise in eCOA system implementation, vendor management, and training

  • Deep understanding of clinical data workflows and regulatory frameworks

  • Excellent leadership, communication, and stakeholder management skills

  • Fluent in English (written and verbal)

Perks & Benefits:

  • Competitive salary (not specified; negotiable based on experience)

  • Annual leave entitlements and global well-being support

  • Comprehensive health insurance packages

  • Retirement planning support

  • Global Employee Assistance Program (24/7 access)

  • Life assurance and other optional country-specific benefits

  • Inclusive, diverse, and accessible workplace culture

Company Description:

ICON plc is a global leader in clinical research and healthcare intelligence, delivering outsourced development services to the pharmaceutical, biotechnology, and medical device industries. With a strong emphasis on innovation and compliance, ICON partners with clients to accelerate the development of life-saving therapies.

Work Mode:

Remote – Based on East Coast USA


Apply Now:

If you’re an expert in eCOA implementation with a passion for driving clinical data transformation, apply today to join ICON’s global mission in advancing healthcare innovation.