Clinical trial supply associate jobs in Summit, New Jersey (NJ) State

Support the Clinical Operations team in executing clinical trials, initially in the US with potential expansion abroad. Ensure proper access controls for clinical trial documentation. Develop and maintain systems for the receipt, tracking, and archiving of clinical trial documents. At least 3 yea...

As the Associate Director, Innovation Capability for Clinical Trial Diversity, you will drive the delivery of innovative solutions for clinical trials in the key focus area of diversity and inclusion. Bachelor's degree in sciences/ healthcare/ technology and 5+ years of clinical trial innovation ...

As the Associate Director, Innovation Capability for Clinical Trial Diversity, you will drive the delivery of innovative solutions for clinical trials in the key focus area of diversity and inclusion. RY9z8wRole Requirements:Essential Requirements:* Bachelor's degree in sciences/ healthcare/ tech...

Clinical Trial Drug Safety Associate. Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. Perform training of s...

As the Associate Director, Innovation Capability for Clinical Trial Diversity, you will drive the delivery of innovative solutions for clinical trials in the key focus area of diversity and inclusion. Bachelor's degree in sciences/ healthcare/ technology and 5+ years of clinical trial innovation ...

You will participate in interviews with our stakeholders to capture user requirements and process flows, lead and participate in design, and build solutions with business users and SAP team members to further extend capabilities and functionalities on our existing Clinical Trial Supply Management...

As the Associate Director, Innovation Capability for Clinical Trial Diversity, you will drive the delivery of innovative solutions for clinical trials in the key focus area of diversity and inclusion. Bachelor's degree in sciences/ healthcare/ technology and 5+ years of clinical trial innovation ...

To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as a Clinical Trial Drug Safety Associate for our August Research location in Sofia, Bulgaria with opportunities to work remotely in ac...

Experience Qualifications+ Strong experience and expertise in end-to-end clinical operations functional understanding and execution, including experience in clinical trial/protocol design and implementation required+ Additional experience and expertise in end-to-end clinical trial execution in on...

You will participate in interviews with our stakeholders to capture user requirements and process flows, lead and participate in design, and build solutions with business users and SAP team members to further extend capabilities and functionalities on our existing Clinical Trial Supply Management...

Associate Director, Clinical Trial Acceleration. Supports the ED/Head, Clinical Sciences, Trial Acceleration and Scientific Alliances with departmental initiatives and the planning, coordination, management, reporting and prioritization of USMA trial acceleration activities. Support Head, Clinica...

As a Clinical Trial Associate Team Manager (CTA TM) you will be in the Trial Strategy and Delivery department and responsible for managing a team of Clinical Trial Associates (CTAs). You will report to the Head of Trial Management and work closely with the Global Clinical Trial Managers (GCTMs), ...

The Clinical Trial Associate (CTA) will support the planning, implementation, and management of clinical trials. The Clinical Trial Associate oversees various aspects of clinical trial activities, delivering timely and quality results while adhering to study protocols and complying with regulator...

Senior Clinical Research Associate. Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... Summary The Head of Clinical Trial (CT) Diversity sits within Global Oncology Clinical Development ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... Responsibilities:Clinical Trial Operational Risk (CTOR) Management:Build and manage GCO CTOR ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... Summary Oversees typically a single non-pivotal trial (small size, standard complexity in design ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... Lead trial feasibility and site identification activities in collaboration with the CRO and the ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... and clinical trial design. In addition, he/she will develop a QSP strategy to address ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... Proactively reaches out and build relationship with key program and study staff at clinical ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... clinical trial data analysis- Develop and maintain necessary programming macros or tools to ...

Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies ... clinical trial data analysis - Develop and maintain necessary programming macros or tools to ...