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Principal Cra

6+ years
Not Disclosed
10 June 5, 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

 

Meta Title

Principal CRA Job Singapore | Remote Clinical Research Role

Meta Description

Apply for Principal Clinical Research Associate (CRA) role in Singapore. Remote opportunity with ICON in pharma clinical trials, site monitoring, and leadership.

Meta Keywords

principal clinical research associate Singapore, remote CRA jobs, clinical monitoring job Singapore, CRO clinical research Singapore, ICH-GCP CRA role, pharma clinical trials, vaccine clinical research


Job Summary

Join ICON, a global leader in clinical research and healthcare intelligence, as a Principal Clinical Research Associate (CRA) based remotely in Singapore. This role offers an exciting opportunity to lead site monitoring, co-monitoring, and clinical trial oversight for innovative pharmaceutical vaccine studies. Ideal candidates will have 6+ years of CRO or pharmaceutical monitoring experience, strong leadership skills, and expertise in ICH-GCP guidelines. Embrace remote work flexibility while driving clinical excellence and contributing to life-saving therapies.


Responsibilities

  • Conduct study-specific training for assigned clinical trials

  • Develop and update monitoring tools with Project Manager (PM) review

  • Create tip sheets and contribute to routine study monitoring updates

  • Review CRA trip reports to ensure compliance and quality

  • Act as back-up Project Manager when needed

  • Attend study-related meetings to support clinical trial progress

  • Manage site monitoring and co-monitoring visits effectively


Required Skills & Qualifications

  • Degree in Pharmacy or related healthcare/science discipline

  • Minimum 6 years of clinical monitoring experience with CRO or pharmaceutical companies

  • Proven leadership abilities in clinical research or CRA roles

  • Excellent communication skills for stakeholder engagement

  • Thorough knowledge of international clinical guidelines (ICH-GCP) and local regulatory requirements

  • Flexibility and willingness to travel as needed for site monitoring


Perks & Benefits

  • Competitive salary (salary range not specified)

  • Various annual leave entitlements to support work-life balance

  • Comprehensive health insurance plans tailored for you and your family

  • Competitive retirement savings plans to secure your future

  • Global Employee Assistance Programme (TELUS Health) providing 24/7 access to health professionals

  • Life assurance and flexible country-specific benefits such as childcare vouchers, gym discounts, travel subsidies, and health assessments

More details: https://careers.iconplc.com/benefits


Company Description

ICON plc is a global clinical research organization specializing in pharmaceutical and biotech clinical trials. Leveraging healthcare intelligence and innovation, ICON drives forward new therapies to improve patient outcomes worldwide.


Work Mode

Remote – Singapore based


Call to Action

Ready to advance your career as a Principal CRA with a global CRO?
Apply now to join ICON’s innovative clinical research team remotely and contribute to breakthrough vaccine development!