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

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

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

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

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

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

Serves as the Regulatory Affairs lead on cross functional MDR project teams Ensures compliance with EU Medical Device Regulations (MDR) and EU guidance throughout the project. Actively participates in EU MDR project teams by attending meetings, collaborating with the project manager and cross functional team members, and communicating regulatory requirements and guidance

Lead and support the qualification and evaluation process for new service providers. Lead with minimal supervision the process of Request for Proposal (RFP) development from service provider selection through final contract execution. Manage the contracting activities including preparation, finalization, and administration of CDAs, MSAs, Service Agreements, Work Orders, C

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Clinical Trial Assistant in South Portland, ME. The Clinical Trial Assistant role will have a direct impact on the organization and the larger clinical industry, making this an amazing career opportunity. RESPONSIBILITIES To provide general administrative support to the M

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 Performs bio analytical methods (Chemistry lab) for various Bio QC Tests on raw ma

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

OVERVIEW We are currently searching for a skilled professional to join a well known client's team as a Medical Safety Reviewer in Columbus, Ohio. The Medical Safety Reviewer role will support the medical safety team by collecting, assessing, processing adverse events for clinical or post marketed products in compliance with applicable regulations, guidelines, researching,

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