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ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
Position Summary
The Clinical Operations Study Lead is responsible for independently managing multiple clinical trials of moderate complexity or managing a broader range of activities on large multi-center studies. The COSL is expected to address site and vendor-related issues, with assistance as needed.
Résumé du poste
Le chef d’étude des opérations cliniques (CEOC) est responsable de la gestion indépendante de plusieurs essais cliniques de complexité modérée, ou de la gestion d’un éventail plus large d’activités concernant de grandes études multicentriques. Le CEOC est censé régler les problèmes liés au centre et aux fournisseurs, grâce à une assistance adaptée.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
***Hybrid. This role will require 3 days a week onsite at our West Point, PA (19486) location. 2 days remote based.
Looking for an individual with ERP system experience (SAP/Ariba preferred).
Current or previous Invoicing or Purchase order experience highly preferred.
Demonstrable Excel skills needed.
Suplpy Chain, Logistics, Inventory experience preferred but not required.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
- Reporting to the Associate Director or Director within FASTR (Feasibility, Activations and Strategy & Tactics of Recruitment), this role will be responsible for providing support to study teams across key programs, to enable acceleration of sponsor clinical studies
- Senior Specialist will play a supportive but critical role in the FASTR Team focusing on the delivery of high quality operational, site feasibility and recruitment deliverables, as needed
- Works in close collaboration with trial management teams and FASTR study start-up, recruitment and feasibility teams to provide key inputs, metrics, and outputs to support study acceleration strategies for program and protocol planning
- Supports across a range of rare disease areas and FASTR Feasibility / Recruitment Leads
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
The Clinical Research Associate may be regionally based and is responsible for the monitoring of clinical trial activities in compliance with FDA regulations, ICH/GCP guidelines and company SOPs, to support New Drug Applications. The CRA will support project teams in the placement, implementation, communication, site management, recruitment and retention (R&R) issue identification and resolution, and activities required at the conclusion of clinical studies, as stipulated in the monitoring plans for assigned projects.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
The Manager, Strategic Relationship Management provides support and assistance in the planning, execution and management of outsourcing for services associated with global clinical trials. The Manager, SRM minimizes regulatory, legal, and financial risks as it pertains to outsourcing agreements and to maintain strategic support relationships.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
The Global Strategic Sourcing (GSS) Analyst provides support and assistance in the planning, execution and management of strategic sourcing for services associated with R&D and global clinical trials. An important part of this role is to minimize regulatory, legal, financial, operation risks as it pertains to Master Service Agreements, Work Orders and Change Orders.
Hybrid Role: Will require 3 days weekly onsite in our Wilmington, DE (19803) office. 2 days home based.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
ICON plc is a world-leading healthcare intelligence and clinical research organization. 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.
The Clinical Budget Analyst is an important member of the Clinical Development Execution team at our client. You will become the “go to” person for broader financial understanding or insight into defined clinical projects, and will have direct responsibility for the financial health of clinical studies. In addition, you’ll be the liaison between Clinical Operations, Outsourcing and Finance, providing oversight support for invoicing and overall study budgets, and you will provide valuable analysis and metrics to help improve the financial management of clinical studies. You’ll be responsible for establishing a solid trusting relationship with Finance and other business relationships throughout the organization. This role is a fantastic opportunity if you want to gain a comprehensive view of clinical processes and financials.
Icon is looking for a Records Management Associate to work office based in Indianapolis, IN. This is an administrative type position that manages the Records Center’s incoming/outgoing documents and files. Position is full time and requires multi-tasking, communication and organizational skills, along with attention to detail.
Icon is looking for a Records Management Associate to work office based in Indianapolis, IN. This is an administrative type position that manages the Records Center’s incoming/outgoing documents and files. Position is full time and requires multi-tasking, communication and organizational skills, along with attention to detail.