Clinical Standards

Associate Clinical Leads are an integral part of clinical trial delivery working alongside clinical teams to improve patients' lives by bringing new drugs to the market faster. · Ensure clinical delivery of assigned projects in compliance with regulatory requirements customer req ...

The Clinical Research Director serves as the Clinical Operations lead for a country or cluster of countries and is responsible for the execution of all clinical trials within the scope of the Global Clinical Trial Operations country organization. · ...

We believe in creating meaningful moments every day for our residents, · their families and our teams. · Provide visible, · supportive and inspirational clinical leadership across · the region to support and develop our Home Managers · and Clinical Care Managers. · ...

The Clinical Research Director serves as the Clinical Operations lead for a country or cluster of countries. · •    Partner with regional leadership to shape and deliver the country or cluster strategy that meets the global clinical research pipeline needs. · Represent the countr ...

The Clinical Research Director serves as the Clinical Operations lead for a country or cluster of countries responsible for execution of all clinical trials within scope. · Ensure trials are conducted to high quality standards. · Provide leadership and oversight of objectives for ...

Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). · Assist with daily worklo ...

+ Job summary · Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. · +Bachelor's De ...

Perform clinical research procedures to collect, record and interpret data on patients enrolled in studies. Assist with workload planning. · ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. · ...

As a Senior or Principal Statistical Programmer in our sponsor-dedicated Flexible Solutions business unit, you will be central to the successful delivery of complex global oncology clinical trials (Phases I–III) for some of the world's most renowned and innovative pharmaceutical ...

We are currently seeking a Study Start Up CRA to join our diverse and dynamic team.As a Study Start Up CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, ...

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. · ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory ...

This job involves performing daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery. · Perform daily administrative activities in conjunction with the Clin ...

Manage the execution of assigned clinical studies from initiation through to closeout. Ensure that clinical study management and project deliverables are on time and in accordance with standard operating procedures (SOPs), policies, and practices. · ...

We're proud to foster an inclusive environment driving innovation and excellence. · We are currently seeking a Study Start Up CRA to join our diverse and dynamic team. · You will play a critical role in overseeing and managing clinical trial activities to ensure they are conducte ...

The Senior Study Start up Specialist will perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations. · Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites. ...

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance act ...

The Clinical Manager is responsible for supporting quality clinical care delivery in a fast-growing organization specializing in mental health services. · Clinical degree (MD, RN, NP) · Experience in clinical operations or management · ...

Leading clinical team to achieve project objectives while optimizing speed quality cost delivery according SOPs policies practices. · Participate bid defense preparations. · Develop maintain clinical project plans including but not limited to clinical operations plan recruitment ...