Clinical Research Associate 2

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...

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...

'¢ Acts as the primary point of contact to Sponsors and Contract Research Organisations (CRO) on enquiries related to clinical research. '¢ Performs feasibility study and revert report in a timely manner '¢ Prepares site and inform & remind team on any pre-qualification visit by Sponsor / CRO. '¢ Assists Investigators / Sub Investigators in preparation...

**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,...

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...

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...

**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,...

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...

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...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

**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...

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...

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...

**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...

**Scope of work** i. Registering patient information, and answering telephone inquiries from patients and others ii. Collects, verifies, records, and maintains data on clinical activity iii. Obtains patient histories, and insurance approvals as appropriate; prepares and updates medical charts and associated records, and enters patient data into files and...

The Clinical Quality Associate Director (CQAD) in general, is responsible for the maintenance and further development, and the communication of high-quality standards in the delivery of clinical studies. This includes a key role in ensuring that the training needs in the local SMM (Site Management & Monitoring) team are fulfilled in cooperation with the...

The Clinical Quality Associate Director (CQAD) in general, is responsible for the maintenance and further development, and the communication of high-quality standards in the delivery of clinical studies. This includes a key role in ensuring that the training needs in the local SMM (Site Management & Monitoring) team are fulfilled in cooperation with the...

**Scope of work** i. Registering patient information, and answering telephone inquiries from patients and others ii. Collects, verifies, records, and maintains data on clinical activity iii. Obtains patient histories, and insurance approvals as appropriate; prepares and updates medical charts and associated records, and enters patient data into files and...

**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...