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

Develops scientific understanding of assigned program and protocol requirements Supports protocol design and development strategy for clinical trials Manages protocol development process; including writing support, reviewing, adjudication/resolution of cross functional comments, and ensuring high quality final document Contributes to the development of Informed Consent Fo

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 an Occupational Health Nurse in Plymouth, MN. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES Provide occupational health services including treatment and care to site pop

Develop a robust timeline and plan for the overall program. Development or improvement of program processes to drive program efficiency Update program trackers and program update reports Assist with PMO deliverables for program health improvement initiative Take on project management remediation process which includes coordinating with program workstream leaders to manage

Draft, review, negotiate, and finalize contracts within the company. Contract types may include vendor service agreements, change orders, clinical trial agreements, assignments and amendments. Performs research on and track contractual obligations within agreements. Manage tracking, filing and maintenance of legal contract records in the legal database. Acts as liaison be

Responsible for the management of assigned clinical trial(s) and the physician training events by leading cross functional teams that may include tasks specific to study start up, regulatory, contract and budgeting, safety, medical monitoring, training event planning, etc. Serves as the clinical trial/project point of contact and the liaison with the CRO, third party vend

Review SOWs and other related contracts to identify, evaluate and negotiate with third party providers, to secure cost effective services and mitigate risk. Create/ Review/ Validate Analytics such as spend reports, savings, and contracts. Analyze market trends, pricing, and industry developments to inform Strategic Sourcing decisions. Lead RFP/RFI of supplier negotiations

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 Process Technician in Exton, PA. Under supervision and guidance, the Process Technician of Upstream Operations will be responsible for hand on executing the routine operation, maintenance, and periodically requalification of cell culture based upstream production equipmen

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Medical Technical Writer, Remote. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES Manages and writes/edits relevant sections of global clinical documents, required for a

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as an Administrative Coordinator in Exton, PA. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES The Administrative Coordinator will prioritize workload and deliver specific cl

The AC Intern will assist the managers or executive leaders across the Staffing & Solutions AC Businesses. In addition, they may support Manager, Directors, and Senior Directors as they identify and pursue new and existing business opportunities. The Intern will support the executive leaders with departmental projects and assist with identifying new client opportunities,

Independently perform the following responsibilities under the direction of the Product Development Manager and/or Program Head to coordinate, manage, and lead the overall execution of clinical studies or group of clinical studies while following appropriate GCPs and SOPs Provide scientific insight into study design and disease process; Lead protocol development and writi

Independently perform the following responsibilities under the direction of the Product Development Manager and/or Program Head to coordinate, manage, and lead the overall execution of clinical studies or group of clinical studies while following appropriate GCPs and SOPs Provide scientific insight into study design and disease process; Lead protocol development and writi