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

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...

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 ...

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 ...

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...

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...

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. ...

Work closely with cross-functional teams supporting the business, including Clinical, Medical Affairs, Regulatory, Compliance, Finance, Procurement, Tax, and other business functions to facilitate consistent and efficient support for clinical trials. Experience drafting and negotiating contracts ...

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. ...

Associate Directors are emerging leaders in the field of quantitative drug development, with a ... clinical trial simulation, disease progression models, quantitative systems pharmacology (QSP ...

Associate Directors are emerging leaders in the field of quantitative drug development, with a ... clinical trial simulation, disease progression models, quantitative systems pharmacology (QSP ...

... supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities ... support of clinical trial objectives. You will be part of a diverse, cross-functional team of ...

Some knowledge of clinical trial methodology and experience in development of strategy and the design of protocols desired. * Works with some supervision and guidance. Exercises judgement within well ...

Actual Title: Associate Principal Scientist Department- Patient-Centered Endpoints & Strategy ... trial and observational studies • Ability to understand and respond to multiple internal and ...

Lead/support/oversee clinical supplies production with respect to device component manufacture and final assembly of biologic/drug product with device constituent part.Lead/support the development ...

Experienced in the life sciences domain and clinical trial processes * Demonstrated ability to influence others without direct authority. * Demonstrated performance as a key contributor to ...

... supply management were integral aspects of the position is strongly preferred. * Valid driver ... Flexible work schedules, clinical training series, leadership development program * 10 paid ...