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...

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...

**Essential Functions** - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines - Administer protocol and related study training to assigned sites and...

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,...

Petaling Jaya, Malaysia **Job ID** R0000017212 **Category** Administrative **ABOUT THIS ROLE**: **Key Accountabilities**: **Data Validation (cleaning)**: - Responsible for/start to lead data cleaning and data review activities (Co-Primary CDA/Primary CDA), e.g. query management and manual/SAS listing reviews. - Support/start to lead data processing...

Petaling Jaya, Selangor, Malaysia **Job ID** R0000020029 **Category** Data Management **ABOUT THIS ROLE**: **Key Accountabilities**: **Data Validation (cleaning)**: - Responsible for/start to lead data cleaning and data review activities (Co-Primary CDA/Primary CDA), e.g. query management and manual/SAS listing reviews. - Support/start to lead data...

Petaling Jaya, Malaysia **Job ID** R0000017833 **Category** Data Management **ABOUT THIS ROLE**: **Key Accountabilities**: **Data Validation (cleaning)**: - Responsible for/start to lead data cleaning and data review activities (Co-Primary CDA/Primary CDA), e.g. query management and manual/SAS listing reviews. - Support/start to lead data processing...

**Job Overview** Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. **Essential Functions** - Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and...

Direct a team of clinical professionals to support and deliver clinical research projects in Singapore and Malaysia, ensuring that projects are effectively resourced and that teams are effectively trained and managed to deliver successful outcomes to customers. Work with senior leadership in formulating and executing effective strategic goals and objectives...

**Responsibilities**: - Initiate investigator site activities, including collection and submission of regulatory documents to Ethics Review Board and Competent Authority, communicate and negotiate budgets and contracts with site, track and ensure site compliance to required training and effectively drive timelines aligned with company priority - Communicate...

Project Management Analysts (PMA) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) providing support with project management activities to mitigate risk, control cost,...

**Duties and Responsibilities** To be an effective academic and to work closely with administrative colleagues to facilitate learning and the development of knowledge through teaching, supervision, student advisory and providing services to the university and community. Lecturer Responsibilities - Preparing and delivering lectures, tutorials, workshops,...

Requirements - Possess at least a Certificate of Diploma for a Clinic Assistant - Pleasant disposition with good communication skills - Must be computer literate - Ability to deal with emotionally charged and pressured situations - Caring and compassionate nature Responsibility - Manage reception area - Assist doctors and clinic in serving and providing...

**Responsibilities** - Conduct pre-sale product demonstrations at healthcare facilities. - Provide post-sale user training to ensure optimal use and feature maximization of the equipment. - Collaborate closely with the sales team to support clinical products before and after sales. - Actively participate in customer service activities to enhance satisfaction...

**Job Overview** CTEs collaborate with research staff and other stakeholders to drive trial recruitment and to support study specific training needs. The CTE acts as a strategic partner to both external and internal stakeholders to optimise the site experience and performance. Leads the relationship management and communication of medical and scientific...

To collect and submit regulatory documents to the Ethics Review Board and Competent Authority, communicate and negotiate budgets and contracts with site. - Track and ensure site compliance to required training and effectively drive timelines aligned with a company priority. - To ensure the investigator sites meet requirements to enroll study participants...

1) To lead bioinformatics studies of the tumour genome and transcriptome for cancers that are common in Malaysia 2) To design and construct genomics and machine learning pipelines to process and analyze genomics and clinical data 3) To perform long-range transfer of genomics data, verify the integrity of the transferred data, as well as perform primary...