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Fsp Cra (Level I)

Thermo Fisher Scientific
Thermo Fisher Scientific
0-2 years
Not Disclosed
10 Jan. 14, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences 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

FSP Clinical Research Associate (CRA I) – Singapore
Location: Singapore | Job Type: Full-Time | Category: Clinical Research | Work Model: Hybrid

Company Overview:
Join Thermo Fisher Scientific / PPD Clinical Research Services, a leading global contract research organization (CRO) delivering high-quality clinical trial services across more than 100 countries. Our teams bring scientific and operational excellence to advance life-changing therapies and improve health outcomes worldwide.

Position Summary:
The CRA I (FSP model) supports site monitoring and management activities for clinical trials, ensuring compliance with study protocols, ICH-GCP, sponsor SOPs, and regulatory requirements. This entry-level CRA role provides a unique opportunity to gain hands-on experience in clinical trial monitoring, site management, and data quality under supervision.

Key Responsibilities:

  • Conduct on-site and remote monitoring visits as per client monitoring plans and SOPs.

  • Verify accuracy, completeness, and source data integrity of clinical trial data.

  • Support site initiation, routine monitoring, and close-out visits under supervision.

  • Ensure timely collection and review of essential documents in line with ICH-GCP and local regulatory requirements.

  • Maintain regular communication with site personnel to ensure protocol adherence, timely data entry, and resolution of issues.

  • Track site performance metrics and follow up on action items to maintain study compliance.

  • Assist with submissions to regulatory authorities (e.g., HSA) and ethics committees (IRB/IEC).

  • Document observations, visit reports, and correspondence accurately and within timelines.

  • Complete administrative tasks, including training, timesheets, and expense reports.

  • Collaborate with project team members and client representatives to ensure consistent study delivery and quality outcomes.

  • Participate in study-specific and corporate training programs to develop monitoring expertise.

Qualifications:

  • Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field.

  • Prior experience in clinical research (e.g., CTA, CRC, or CRA trainee) preferred.

  • Foundational knowledge of ICH-GCP, clinical trial operations, and local regulatory requirements.

  • Strong organizational, communication, and interpersonal skills.

  • Ability to work under supervision and develop independent clinical monitoring skills over time.

Why Join Us:
This role offers hands-on clinical research experience in a global CRO environment, structured mentorship, and professional development opportunities to kick-start your career in clinical operations.