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Principal Cra

6+ 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

 

Meta Title

Principal CRA – Clinical Research | Singapore

Meta Description

Join ICON as a Principal CRA in Singapore. Lead vaccine trials, manage clinical sites, and drive regulatory compliance in a remote role.

Meta Keywords

Principal CRA, Clinical Research Associate, remote CRA jobs, ICON Singapore, ICH-GCP, vaccine trials, site monitoring, pharma jobs Singapore, CRO careers


Job Title: Principal CRA – Remote (Singapore)

Location: Singapore (Remote)
Company: ICON plc
Job Type: Full-time
Industry: Clinical Research, Pharmaceuticals
Compensation: Competitive salary (not specified in listing)


Job Summary

ICON plc is hiring a Principal Clinical Research Associate (CRA) to lead the monitoring of global vaccine trials for one of the top pharmaceutical sponsors. Based remotely in Singapore, this senior CRA role offers an opportunity to lead site management activities, contribute to protocol compliance, and ensure clinical trial success across phases II–IV. You’ll work in a collaborative, high-performing environment committed to global health advancement.


Key Responsibilities

  • Deliver study-specific training and support for assigned trials

  • Lead the creation of monitoring tools, tip sheets, and documentation with PM input

  • Conduct reviews of CRA trip reports and provide actionable feedback

  • Serve as back-up Project Manager (PM) when necessary

  • Participate in study-related meetings, providing insights and leadership

  • Conduct site monitoring and co-monitoring visits across assigned locations

  • Ensure adherence to international (ICH-GCP) and local regulatory guidelines


Required Skills & Qualifications

  • Degree in Pharmacy or Life Sciences

  • 6+ years of monitoring experience in clinical trials, preferably in vaccines

  • Proven leadership abilities in a similar CRA role

  • Strong knowledge of ICH-GCP and applicable regulatory requirements

  • Excellent verbal and written communication skills

  • Availability to travel for on-site visits as required


Perks & Benefits

  • Competitive salary (details not disclosed)

  • Annual leave entitlements based on location policies

  • Comprehensive health insurance for self and family

  • Global retirement planning and savings programs

  • 24/7 Global Employee Assistance Program via TELUS Health

  • Life assurance and wellness support programs

  • Country-specific flexible benefits: childcare vouchers, travel passes, gym discounts


About ICON plc

ICON plc is a world leader in clinical research and healthcare intelligence. With a mission to accelerate the development of life-saving medicines, ICON partners with leading pharmaceutical, biotechnology, and medical device organizations to deliver high-quality, data-driven solutions globally.


Work Mode

Remote (Singapore-based) – Travel required for site visits


Call to Action

Are you an experienced CRA ready to take the next step into leadership with one of the most respected CROs globally? Apply now to become a Principal CRA at ICON and help bring vital treatments to market faster, safer, and smarter.

Apply on ICON Careers Website