Clinical Research Associate Jobs in Singapore

Clinical Research Associate (Senior) at Novartis Singapore, part of the Clinical Trials team, drives site monitoring and partnership across Phase I–IV studies. The role leads site initiation, remote and onsite monitoring, risk mitigation, and audit readiness while collaborating with internal stakeholders.

Clinical Research Associate II at FTSIN Fortrea Singapore Pte Ltd drives site monitoring for clinical trials, ensuring compliance with ICH GCP and local regulations. The role manages site visits, data integrity checks, and regulatory documentation while coordinating with sponsors and study teams.

Intern Clinical Research Associate at Merck will serve as the primary site contact and manager for clinical studies across all phases. Responsibilities include site relationship development, compliance with ICH‑GCP, sponsor SOPs, local regulations, and protocol requirements.

Senior Clinical Research Associate at IQVIA responsible for site selection, initiation, monitoring, and close‑out visits, developing recruitment plans, administering protocol training, ensuring quality and regulatory compliance, and managing data queries. Works with global trials, collaborates with customers, and follows GCP and regulatory requirements.

Clinical Research Associate II responsible for site management and monitoring of clinical trials per Fortrea SOPs, ICH GCP, and sponsor requirements. Duties include site initiation, routine and close‑out visits, data integrity checks, eCRF review, IP inventory, audit readiness, and travel to study sites (~60%).

Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned. Responsible for all aspects of site management as prescribed in the project plans.

Senior Clinical Research Associate responsible for site monitoring and management across clinical studies. Leads monitoring visits, ensures protocol compliance, reviews CRFs, generates queries, and resolves data issues.

As you develop your career as a Senior CRA or CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You will be exposed to wider opportunities like operations management, dedicated customer solutions, project management and more.

Clinical Research Associate Manager at Novartis Singapore leads a team of CRAs, overseeing performance, coaching, and resource allocation for clinical trials. The role manages vendor relationships, monitors compliance with GCP/ICH standards, and supports audits and inspections.

Clinical Research team at Thermo Fisher Scientific conducts oncology trials across global sites. The Clinical Research Associate I monitors investigator sites, performs risk‑based assessments, ensures ICH‑GCP compliance, and documents findings both remotely and on‑site.

Clinical Research Associate 2 responsible for monitoring clinical sites, conducting routine monitoring, closeout, and pre-study visits. Maintains study files, liaises with vendors, and manages sites per project plans.

Clinical Research Team at Thermo Fisher Scientific supports global clinical trials by coordinating site activities and ensuring regulatory compliance. The Assistant Clinical Research Associate provides remote support for site preparedness, documentation, and logistics, assisting CRAs with monitoring, data collection, and vendor coordination.

Join Thermo Fisher Scientific as a Clinical Research Associate to support global clinical trials. In this role you will conduct on‑site and remote monitoring visits, ensuring protocol compliance, data integrity, and regulatory adherence.

Clinical Research Coordinator at IQVIA in Singapore supports investigator team in clinical trials, managing patient consent, randomization, e-questionnaire training, follow-up visits, and site file maintenance. Coordinates patient support programs, monitors project schedules, ensures data protection compliance, updates databases, prepares presentations, and maintains communication with stakeholders.

Join Our Team at the School of Biological Sciences, Nanyang Technological University, Singapore The School of Biological Sciences (SBS), part of the College of Science, was established in 2002 with a mission to advance biological and biomedical sciences. At SBS, our research spans various areas, including infectious diseases, immunology, neurodegenerative diseases, telomere biology, and genome function.

HELIOS Study team at LKCMedicine conducts a large-scale population health study to profile up to 100,000 Singapore residents, collecting surveys, physical measurements, and biomarkers. The Senior Executive, Clinical Research Officer, Operations will manage participant communications, administer questionnaires, collect samples, troubleshoot equipment, monitor supplies, and ensure compliance with protocols and Good Clinical Practice.

HELIOS Study team at LKCMedicine conducts a large-scale Singapore population health study, gathering health, lifestyle, and biomarker data. The Senior Executive Clinical Research Officer, Reporting ensures accurate participant communication, compiles health reports, manages honoraria, and coordinates follow‑up on critical findings.

The Lee Kong Chian School of Medicine (LKCMedicine) trains doctors who put patients at the centre of their exemplary care. The School, which offers both undergraduate and graduate programmes, is named after local philanthropist Tan Sri Dato Lee Kong Chian.

HELIOS Study team at LKCMedicine, a flagship Singapore population health study, conducts large‑scale health surveys, physical measurements and biomarker analyses. The Senior Executive (Clinical Research Officer, Biobanking) manages receipt, processing and storage of biological samples, oversees equipment maintenance, quality control and procurement, and supports frozen sample retrieval for collaborators.

LKCMedicine’s Clinical Research Officer joins the HELIOS-BEAM study team to advance digital mental health screening. The role manages participant recruitment, consent, data integrity, and protocol compliance, ensuring high-quality evidence for scalable digital biomarkers.