Clinical Research Coordinator

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...

**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...

**Responsibilities include, but are not limited to**: - Main Point of Contact (POC) for assigned protocols and link between Country Operations and clinical trial team (CTT). - Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and performance of deliverables/timelines/results to meet country...

1. Plan and managing the types of information collected from patients, healthcare providers and medical researchers from Beacon Hospital 2. Provide support to the clinical research department on analytics execution 3. Manage and processing the raw datasets and conducted statistical analysis. Data sources include medical and pharmacy claims data, hospital...

The Clinical Operations Leader is responsible for coordinating the functional team members and their activities across all geographies, liaising with project leadership and the sponsor to ensure that the Clinical Operations deliverables (timeline, quality, productivity) are met. The Clinical Operations Leader has overall accountability for the execution of...

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...

**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...

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**: - 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,...

**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,...

**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,...

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...

**Clinical Trial Managers** are an integral part of clinical trial delivery, working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Clinical Trial Manager is a member of the core project team responsible for the clinical delivery of clinical studies to meet contractual requirements in accordance with...

**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...

**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...

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...

**Assist or coordinate clinic functions efficiently and effectively by: -** - Handling, tracing and tracking medical records of patient in clinic to/ from the Medical Record Department / counter prior or after the clinic session. - Maintain confidentiality and safety to all patient’s record. - Perform Assessment (weight, height and vital signs) of patient...

**Job Summary**: 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. **Clinical Instructor Responsibilities** - Supervise all clinical activities and working of all student...