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

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

Work on life cycle management product test assignments. Experience in testing of mechanical, electrical, and electromechanical products. Contribute to test data analysis as needed. Collaborate with test technician team and engineering in achieving project goal. Be a part of root cause investigation analysis as needed EXPERIENCE Minimum of three years of experience in test

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a QC Technician III in Saint Joseph, MO. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES/EXPERIENCE Perform microbiological methods including microbial identification and

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Stability Associate II in New Haven, CT. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES When we put unexpected teams in the same room, we unleash bold thinking with the

Works on non routine to routine problems where analysis of situations or data requires an evaluation of identifiable factors. With guidance may exercise independent judgment in developing methods, techniques and evaluation criteria for obtaining results. Ensures record tracking of pertinent data is being completed through computerized systems. Analyzes non routine informa

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

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 Sourcing Manager in Ridgefield, CT. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES Duties Implement complex Category Strategy following TOM and develop it for corporate

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Regulatory Specialist II in Alameda, CA. Their work will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES Responsible for regulatory activities, including product registrations, impact a

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 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

Independently negotiates initial or amended site Clinical Trial Agreements (CTAs) and budgets, and/or serves as escalation point and oversight for CROs negotiating site CTAs and budgets in support of assigned global Clinical Studies. Independently negotiates other initial or amended clinical Agreements such as Investigator Initiated Research Agreements (IIRs), Confidentia

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

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