# FSP CRA (Level II) [Thermo Fisher](https://www.jorb.ai/firms/thermo-fisher.md) · Singapore · [None](https://www.jorb.ai/jobs/none.md) Thermo Fisher is hiring a FSP CRA (Level II) in Singapore. Posted 2026-06-04; applications close 2026-08-03. **Apply**: https://jobs.thermofisher.com/global/en/job/TFSCGLOBALR01352257EXTERNALENGLOBAL/fsp-cra-(level-ii) Posted 1mo ago. ## Role details ## Job Description **Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation** We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global FSP team, you will perform and coordinate all aspects of clinical monitoring and site management activities in close collaboration with the sponsor. As a Clinical Research Associate (Level II), you will conduct both on-site and remote monitoring visits to ensure protocol and regulatory compliance, as well as proper documentation. Acting as a site management specialist, you will ensure that clinical trials are conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable local regulations, and SOPs. You will play a key role in ensuring subject safety, data integrity, and inspection readiness, while building strong relationships with investigational sites and sponsor stakeholders. ### What You’ll Do - Perform on-site and remote monitoring visits using a risk-based monitoring approach, including SDV, SDR, and source data review as applicable - Apply root cause analysis (RCA), critical thinking, and problem-solving skills to identify site issues and implement corrective and preventive actions - Ensure investigational sites comply with protocol, ICH-GCP, and applicable local regulatory requirements - Review investigational product accountability, including physical inventory and documentation - Prepare monitoring visit reports, follow-up letters, and other documentation in a timely and high-quality manner - Escalate issues and follow through to resolution in collaboration with the CTM and sponsor team - Maintain regular communication with sites between visits to ensure ongoing compliance and data quality - Participate in site selection, site initiation, routine monitoring, and close-out activities - Ensure essential documents are complete and maintained in compliance with ICH-GCP and applicable regulations - Update study systems (e.g. CTMS) and provide study progress updates to the CTM as required - Facilitate effective communication between investigational sites, sponsor, and internal project teams - Support audits and inspections by ensuring audit readiness at site level - Complete administrative tasks (e.g. expense reports, timesheets) in a timely manner - Contribute to process improvements and team initiatives as applicable ### Education and Experience Requirements - Bachelor’s degree in life sciences or a related field, or Registered Nurse qualification - Minimum 1–2 years of clinical monitoring experience (or equivalent), or completion of a recognized CRA training program - Experience working in an FSP or sponsor-dedicated model is preferred - Experience in site management and monitoring within Singapore is preferred - Familiarity with local regulatory requirements (e.g. HSA) and site practices is an advantage - Valid driver’s license is preferred (if applicable) ### Knowledge, Skills and Abilities - Solid clinical monitoring skills with understanding of risk-based monitoring concepts - Working knowledge of ICH-GCP, local regulatory requirements, and clinical trial processes - Strong critical thinking and problem-solving skills - Effective communication skills in English (additional regional language skills are a plus) - Strong stakeholder management skills, including working with sponsor teams - Good organizational and time management skills - Attention to detail and commitment to quality - Ability to work independently and collaboratively in a team environment - Proficiency in Microsoft Office and ability to learn relevant systems ### Working Conditions and Environment - This is a hybrid role, combining home-based work with on-site monitoring visits - Regular travel to investigational sites within Singapore - Occasional presence at sponsor or office locations may be required - Work may involve exposure to clinical environments ## Applying to this role This FSP CRA (Level II) role at Thermo Fisher runs through the firm's own careers portal and expects a CV and cover letter written specifically for the posting, not a portable submission carried across firms. Jorb AI's application agent tailors a CV and cover letter from your background to this posting and tracks the role alongside the rest of your applications. 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