Working under the supervision of the Administrative Director of the CNCT and the Principal Investigator and following established policies and procedures, coordinates clinical research studies. May be responsible for the following activities recruiting and evaluating patients for studies; collecting and organizing patient data; attending and collecting human specimens dur

SmithGroup is an award winning, multinational integrated design firm with a team of 1,300 experts across 19 offices in the U.S. and China. We employ research, data, advanced technologies and design thinking to help clients solve their greatest challenges. Our specialistsdevelop beautiful, sustainable, future focused solutions for healthcare providers, science and technolo

SmithGroup is an award winning, multinational integrated design firm with a team of 1,300 experts across 19 offices in the U.S. and China. We employ research, data, advanced technologies and design thinking to help clients solve their greatest challenges. Our specialistsdevelop beautiful, sustainable, future focused solutions for healthcare providers, science and technolo

SmithGroup is an award winning, integrated design firm that blends research, data and technology with innovation and a creative spirit to deliver resilient, inclusive spaces that solve our clients' greatest challenges. Our teams create exceptional design solutions for healthcare, science and technology, workplace, mixed use, higher education, cultural, waterfront, parks a

Perform timely and accurate evaluations and analysis of raw materials, products, processes, and facilities that support the efficient manufacturing and shipment of quality products according to specifications at our manufacturing facility. Requirements Responsible for all aspects of food safety and quality as defined in plant and department procedures. Collect, analyze, a

The assigned publication programs will be global, may be complex, and of business importance to Client and Client's reputation, requiring multi functional leadership experience to achieve program goals Ensure Client's company sponsored publication activities are conducted according to good publication practices (including ICMJE, GPP3, CONSORT, etc) and Client's Global Pub

Job Title QC Associate Job ID 24 02046 Location Devens, MA Duration 06 Months contract on W2 Onsite, Devens Work Schedule Mon Fri, Business Hours This position will perform routine testing including media and reagent preparation, cell maintenance and working closely with several instrumentations used for Bioassay testing. Education and Experience Required BS with minimum

We are seeking a self motivated, detail orientated, and collaborative team member to partner effectively with research staff and support day to day laboratory operations at our new flagship building in Cambridge, MA. The successful candidate will be part of the Lab Operations (Lab Ops) team within Strategy & Research Operations and will play a critical role in maintaining

Under the direction of a member of the faculty, the Bioinformatician is responsible for the design, development, evaluation and iterative modification of a technical infrastructure to expedite the quantitative evaluation of data resulting from studies that are laboratory based. The position will entail the establishment and maintenance of applicable in house bioinformatic

Primary Work Address 16 Divinity Avenue, Cambridge, MA, 02138 Current HHMI Employees, click here to apply via your Workday account. The Howard Hughes Medical Institute (HHMI) advances the discovery and sharing of scientific knowledge to benefit us all. As a biomedical research organization and philanthropy, HHMI supports a vibrant community of academic researchers, educato

Work with a team of multidisciplinary scientists to deploy gene editing (such as base editing and prime editing), delivery (such as AAV), and protein evolution technologies developed in the lab) Advance current technologies to incorporate new biological and therapeutic models, genotypic readouts, and data acquisition and computational analysis approaches Identify goals, f

This individual will support method development, validation, and quality control activities conducted at Sarepta Andover in compliance with cGMP regulations. The individual will devise, troubleshoot, and validate cell based assays to assess the critical quality attributes of AAV gene therapy products including potency and infectivity. This role would facilitate activities

The Associate Director, QC Cell Culture and Bioassay will be responsible for overseeing a testing laboratory charged with the execution of all GMP bioassay testing (release and stability) related to Sarepta' s Gene Therapy pipeline. The Associate Director will build and oversee a team of eight to ten QC technicians with responsibilities that include but are not limited to

of Role Manage the Investigator Sponsored Trial program across the Lantheus Medical Imaging portfolio for all Lantheus assets, including all processes related to multiple functional areas. Essential Functions Independently manages tracks and monitors the Global Investigator Sponsored Trial program across all Lantheus assets and ensure that compliance with SOPs is documente

This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. PRINCIPAL DUTIES AND ESSENTIAL FUNCTIONS Responsible for assisting in the recruitment of study participants. Assesses potential patients and eligibility for inclusion in a particular protocol based on protocol requirements. Reviews all eligibility