Assist Associate Director and senior leadership in the management of the outsourcing, vendor selection and clinical contracts process Generate RFIs, RFPs, and contract templates Assist Clinical Trial Managers with quarterly internal budget forecasts of clinical projects Assist Associate Director with costing trials for internal planning purposes Negotiate and maintain cli

Ensure clinical trials are conducted in compliance with protocol/amendment(s), with ICH GCP, SOPs and with applicable regulatory requirements in the assigned countries and sites Ensure subject safety and verify diligence in protecting the confidentiality and wellbeing of study subjects Verify adequacy, completeness, reliability, and quality of trial data collected at stud

The Senior Director, Business Development, effectively identifies and pursues new and existing business opportunities while enhancing relationships with existing clients, keeps abreast of industry trends, competitors' services and acquisitions, and works in conjunction with leadership to develop and respond to new and existing business development opportunities. The Senio

The Vice President, Business Development, is accountable for leading daily performance management and the results of the business development staff assigned. Through daily coaching and training, in addition to leading enterprise level accounts and business opportunities, this role drives sales outcomes as well as the development of existing staff. The Vice President, Busi

The Manager, Data Management is responsible for managing all aspects of data management activities and assigned direct reports to ensure all time frames and targets are met. The Manager, Data Management may serve as portfolio level oversight or as Biometrics Project Manager for data management and biostatistics stand alone programs. Responsibilities Onboarding of new empl

The Senior Grants and Contracts Manager works under limited supervision and guidance of management. This position is primarily responsible for creating, collaborating and negotiating investigator budgets and contracts. Responsibilities Maintains a flexible approach to address issues innovatively and proactively. Provides the Business Development and Proposal teams with gr

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Regulatory Affairs Associate in Abbott Park, IL. As a professional in the Regulatory Affairs function, the individual will assist teams in the registration of products by preparing documentation needed for registration in EURI/MENAP global. Their work will have a direct i

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Medical Director/Clinical Trial Physician remotely. The Clinical Trial Physician will play a key role in a large global phase 3 lupus outcome study. In addition to the responsibilities described below, the CTP will be specifically responsible for reviewing participants me

SOP Strategy and Development Lead revision and development of standard processes for the Clinical Development Team to ensure that all clinical research activities are conducted consistently and in compliance with applicable regulations and standards. Provide GCP guidance for clinical research activities and drive continuous improvement in all processes associated with the

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Regulatory Specialist in Des Plaines, IL. The Regulatory Specialist role will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES Responsible for implementing and maintaining the effectiven