Clinical Research Analyst

1. Primary point of contact to Sponsors and Contract Research Organisations (CRO) on enquiries related to clinical research. 2. Prepare site and inform & remind team on any pre-qualification visit by Sponsor / CRO. 3. Assist Investigators / Sub Investigators in preparation of required documents for ethics submission to Clinical Research Associate (CRA from...

Job DescriptionClinical Research Associate (CRA) Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR AsiaWe were awarded ‘Sponsor of the Year’ in 2019, 2020 and 2022 from Clinical Research Malaysia for the highest number of studies and total study value recorded in the country!We have a proud legacy of turning breakthrough...

Job DescriptionClinical Research Associate (CRA) Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR AsiaWe were awarded ‘Sponsor of the Year’ in 2019, 2020 and 2022 from Clinical Research Malaysia for the highest number of studies and total study value recorded in the country!We have a proud legacy of turning breakthrough...

Minimum Qualification Requirements - At least Bachelor’s degree preferably in a scientific or health related field, postgraduate degree is also welcomed - 1-4 years clinical research experience or relevant experience preferred Understanding of the overall clinical development paradigm and the importance of efficient site activation - Applied knowledge of...

387381BR **Principal RWE Research Analyst**: Malaysia **About the role** Location: #LI-Hybrid About this role: The Principal Real World Evidence (RWE) Research Analyst is responsible for the scientific and methodological aspects of all RWE projects as well as providing guidance for other members of the team. **Your Responsibilities**: Your...

The CRM is accountable for execution and oversight of local operational clinical trial activities and has ownership, oversight and impact on local regulatory and financial compliance, at a country operations level at the client in compliance with ICH GCP and country regulations. The position has a significant impact on how a country can deliver...

Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an...

Job DescriptionThe role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements...

1. Primary point of contact to Sponsors and Contract Research Organisations (CRO) on enquiries related to clinical research.2. Prepare site and inform & remind team on any pre-qualification visit by Sponsor / CRO.3. Assist Investigators / Sub Investigators in preparation of required documents for ethics submission to Clinical Research Associate (CRA from...

1. Primary point of contact to Sponsors and Contract Research Organisations (CRO) on enquiries related to clinical research.2. Prepare site and inform & remind team on any pre-qualification visit by Sponsor / CRO.3. Assist Investigators / Sub Investigators in preparation of required documents for ethics submission to Clinical Research Associate (CRA from...

Job DescriptionClinical Research Associate (CRA) Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR AsiaWe were awarded 'Sponsor of the Year' in 2019, 2020 and 2022 from Clinical Research Malaysia for the highest number of studies and total study value recorded in the countryWe have a proud legacy of turning breakthrough science...

Job DescriptionClinical Research Associate (CRA) Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR AsiaWe were awarded 'Sponsor of the Year' in 2019, 2020 and 2022 from Clinical Research Malaysia for the highest number of studies and total study value recorded in the countryWe have a proud legacy of turning breakthrough science...

Job DescriptionClinical Research Associate (CRA) Based in Malaysia, named one of the Best Companies to Work for in 2019 by HR AsiaWe were awarded 'Sponsor of the Year' in 2019, 2020 and 2022 from Clinical Research Malaysia for the highest number of studies and total study value recorded in the countryWe have a proud legacy of turning breakthrough science...

1. Primary point of contact to Sponsors and Contract Research Organisations (CRO) on enquiries related to clinical research.Prepare site and inform & remind team on any pre-qualification visit by Sponsor / CRO.Assist Investigators / Sub Investigators in preparation of required documents for ethics submission to Clinical Research Associate (CRA from Sponsor /...

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficient...

395165BR **Principal RWE Research Analyst (Japanese/Mandarin Speaker)**: Malaysia **About the role** Location: #LI-Hybrid About this role: The Principal Real World Evidence (RWE) Research Analyst is responsible for the scientific and methodological aspects of all RWE projects as well as providing guidance for other members of the team. **Your...

**Responsibilities**: - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution, filing,...

**Responsibilities**: - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines. - Assist the clinical team with the preparation, handling, distribution, filing,...

Plan and managing the types of information collected from patients, healthcare providers and medical researchers from Beacon Hospital - Provide support to the clinical research department on analytics execution - Manage and processing the raw datasets and conducted statistical analysis. Data sources include medical and pharmacy claims data, hospital data,...

Key Accountabilities:Start-up (from site identification through pre-initiation:Act as Parexel’s direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.Build relationships with investigators and site staff.Conduct, drive and manage country specific feasibility and/or site pre-qualification and...