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BeOne is seeking a CRA II to monitor oncology and hematology trials in Malaysia, working from home with a focus on data quality and timely study conduct. The role requires adherence to ICH‑GCP, local regulations, and BeiGene standards.The successful candidate will have a life sciences degree and relevant monitoring experience, fluent English, and strong...

BeOne Medicines seeks a Senior Clinical Research Manager in Kuala Lumpur to oversee clinical monitoring activities and guide the CRA team, ensuring compliance with ICH‑GCP, local regulations, and company SOPs. This role leads a high‑performing team and promotes a positive collaborative culture.The position requires 7+ years in pharma/CRO, 4+ years of...

Merck & Co., Inc. is seeking an Associate Director (CRAM) to lead a team of CRAs, ensure strong monitoring of clinical trials, and maintain compliance with local regulations and ICH GCP. The role involves talent development, mentoring, and coordinating with country PLMs to align monitoring functions.Key duties include capacity planning, resource allocation,...

MSD Malaysia is seeking an Associate Director (CRAM) to lead a team of 6–14 CRAs and drive high-quality monitoring of clinical trials in Malaysia. The role ensures adherence to local regulations, SOPs and ICH-GCP, while mentoring CRAs and optimizing resource allocation.Reporting to the CRD or Head of Site Management and Monitoring, you will collaborate...

IQVIA LLC in Kuala Lumpur is seeking a Clinical Trial Assistant to support daily administrative activities with CRAs and RSU teams. You will help maintain TMF documents, prepare and archive clinical reports, and assist with study file reviews to ensure timely, compliant delivery.This role requires strong English communication, solid organizational skills,...

IQVIA in Malaysia seeks a diligent Start-up Specialist to lead feasibility, site identification, and contract negotiations for clinical studies. You will coordinate country-specific submissions, prepare SIS/ICFs, and ensure timely data entry into CTMS across assigned countries.The role requires Bachelor’s in life sciences, strong GCP/ICH knowledge, and...

Job Description General Description: The Senior Clinical Research Manager oversees clinical monitoring activities and the CRA team's performance to ensure they comply with ICH‑GCP, local regulations, and company SOPs, and maintain quality across clinical trials. As a line manager, this role leads a team to achieve organizational goals and ensure high...

Summary of Responsibilities: • Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. • Conducts site monitoring responsibilities for clinical trials according to Fortrea’s...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate I – Make an Impact at the Forefront of InnovationWe 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...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of InnovationWe 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...

Aktualnie Poszukujemy Kandydatek/Kandydatów Na Stanowisko Kierownik Projektu / Kierowniczka Projektu Miejsce pracy: Jasin (obok Swarzędza) oraz w delegacji zagranica Numer Referencyjny Zakres obowiązków: • podtrzymywanie dobrych relacji z Klientami firmy; • nadzorowanie prac zespołu wyznaczonego do realizacji kontraktu; • czynny udział w...

Job Overview:As an CRA I, you will be responsible for site monitoring and study management activities to ensure compliance with study protocols, ICH-GCP guidelines, regulatory requirements, and sponsor expectations. You will serve as the primary contact for assigned sites while maintaining patient safety, data integrity, and investigational product...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of InnovationWe 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...

About Us and follow us on LinkedIn and X (formerly known as Twitter). BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.Conducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard...

Planet Pharma is seeking a Clinical Research Associate in Malaysia to lead site initiation, monitoring, and close-out of Phase II–IV trials. You will ensure compliance with ICH-GCP and regulatory standards while coordinating with sponsors and global teams. The role requires strong documentation, budget awareness, and potential mentoring of junior CRAs in a...

Emerald Clinical Trials is seeking an experienced Site Contracts Lead to join our Project Management team. You will drive contract development, negotiate terms with sites, and manage budgets across multiple studies.This hands-on role requires strong negotiation skills, a legal background, and the ability to collaborate with sponsors, vendors, and clinical...

BeOne Medicines is seeking a Clinical Research Associate (CRA) to monitor Oncology and Hematology trials in Malaysia. You will perform site initiation, data collection, and closeout activities in line with GCP/ICH and local regulations.Join a global oncology company advancing affordable treatments. You’ll conduct monitoring visits, prepare reports, and...

BeOne Medicines in Malaysia seeks an Associate Director, Regional Clinical Study Management (SEA) to lead regional trial strategies and a high-performing team across Southeast Asia. You will align portfolio delivery with Global Clinical Operations goals, ensuring timelines, budgets, and quality are met.In this role, you will partner with cross-functional...

MSD in Malaysia seeks an Associate Director (CRAM) to lead a team of 6–14 CRAs, ensuring strong trial and site performance in line with local regulations, SOPs and ICH GCP.The role emphasizes talent development through training, support and mentoring, and collaboration with country PLMs and HQ for resource planning and alignment.Mandatory experience...