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R & D Jobs in Allston, Massachusetts

952 jobs

Overview: The Research Assistant (Animal Physiology Core) coordinates and conducts the services for a core physiology laboratory for the evaluation of animal behavior, physiology, and metabolism in rodent models. Responsibilities: Performs research procedures on mice including but not limited to blood pressure monitoring, body mass composition, hypoxia/hyperoxia experiments, telemetry, behavior...
Job Number: 440163 Principal Statistician OVERVIEW: The purpose of this position is to provide compound level / development phase statistical expertise and leadership by: * Independently designing, analyzing and interpreting clinical studies at a compound level for early phase or less complex programs. * Providing strategic statistical input for feasibility assessments, development plans, cro...
Our client, a global consumer products manufacturer operating in the durable goods, components and consumer electronics space, is looking for an Assistant Manager - R&D to form part of the leadership team in their new office in Cambridge. This position would suit a PhD graduate with the ability to drive the search for new ideas and product innovation in a high-growth environment. Client Details ...
Title: Associate Clinical Operations Lead Location: Cambridge, MA Duration: 12 Months Job details: Under the direction of the Clinical Operations Leads, the Contract Associate Clinical Operations Lead is responsible for the successful oversight and management of clinical trial execution. Manages multiple aspects of the study, ensuring timely and high quality completion of study deliverables. E...
CLINICAL OPERATIONS CONSULTANTS: MANAGER & ASSOCIATE MANAGER Globally recognized Biotech leader with commercially marketed products, and with one of the most robust pipelines in the industry is seeking to expand its Clinical Operations team with two long term Clinical Operations Consultants. The Company doubled its sales in 2015-16 with projections exceeding Wall Streets analysis for this publicl...
Responsibilities of the Food Scientist: Participate in the testing and development of fluid and cultured Products Procure raw materials and technical information needed for development Prepare and process pilot plant prototypes Participate in production trials and commercialization Record test procedures and observations Coordinate product evaluations Lead shelf life testing of fluid and cu...
Review/audit of non-clinical documents to support the preparation for the development of an NDA submission to the FDA and MAA submission to the EMA to support an indication in oncology. Tasks include: Audit of 8 GLP "non clinical" (pre-clinical) study reports Audit of 68 non-GLP non-clinical study reports Reports range in size from 3 pages to 2298 pages (average is 222 pages) Results/findings...
Laboratory Specialist Lexington, MA 5 Mos Responsibilities Assist in the evaluation of the growth, metabolism and product expression of candidate cell lines in bench-scale bioreactors and shake-flasks. Daily activities include cell culture sampling, cell counting, and metabolite analysis, sample submission for product analyses as well as data management and analysis. The candidate will gain ...
BASIC SUMMARY: Initiate, direct and execute projects of diverse scope in a GLP environment, working independently (with peer guidance as needed) or as part of a multi-disciplinary team. Develop strategies, applying broad scientific principles and concepts for the preclinical assessment of treatment modalities including pharmaceuticals and medical devices. ESSENTIAL DUTIES AND RESPONSIBILITIES: R...
Development Engineer - Lexington, MA Currently seeking a Development/Bioprocess Engineer with cell culture knowledge/experience. You would be responsible for assisting in the evaluation of the growth, metabolism and product expression of candidate cell lines in bench-scale bioreactors and shake-flasks. Daily Responsibilities: Cell culture sampling, cell counting, metabolite analysis, sample sub...
COMPANY SEEKS SENIOR R&D ENGINEER LeMaitre Vascular is a leading global provider of innovative medical devices for the treatment of peripheral vascular disease. We develop, manufacture and market disposable and implantable vascular devices to address the needs of vascular surgeons and interventionalists. The company is listed on NASDAQ General Purpose of the Job: Works as member of multi-discip...
Job Title: Development Engineer Location: Bedford, MA Duration: 12 months+ Job Description: Development Engineer As part of the R&D organization, the successful candidate will design novel products to be used in the processing and purification of biopharmaceuticals. This position will be based at our Bedford, MA campus, with some local travel to internal/external manufacturing sites. The ca...
Fixed Assets Manager Job Location:Wilmington, MA Responsibilities BASIC SUMMARY: Responsible for reviewing/analyzing the transaction activities completed by the accountants as well as overseeing the fixed asset process.Responsible for developing global fixed asset processes and lead continuous improvement activities. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Manage the global fixed asset func...
Perform quality assurance checks on radiographic and photographic medical imaging data to ensure protocol specific requirements are met Perform established image processing techniques (converting imaging formats, performing preliminary measurements of lesions and volumes) across multiple modalities (including but not limited to CT, MRI, Ultrasound) using proprietary software as well as other thir...
Auto req ID 9126BR Title Watson Health - Client Experience Center Manager Job Description Ready to change the way the world works? IBM Watson uses Cognitive Computing to tackle some of humanity’s most challenging problems - like revolutionizing how doctors research cancer or transforming how care is delivered to citizens. This is a crucial role for Watson Health and a phenomenal opportunity for...
MSL training (does not have to be a trainer) a. Assist with delivery of data training (live and webex) to MSLs, internal medical affairs personnel, partner companies – mostly all planned, just needs to be delivered b. Assist with content development, as needed c. We are currently onboarding 2 x waves of new hire MSLs through an intensive 6-week program, which is due to complete at the end of Au...
The purpose of this position is to provide compound level / development phase statistical expertise and leadership by: - Independently designing, analyzing and interpreting clinical studies at a compound level for early phase or less complex programs. - Providing strategic statistical input for feasibility assessments, development plans, cross-study analyses and regulatory submissions. - Improv...
This individual is expected to contribute to the development and implementation of CMC regulatory strategy for biologic products in development, with minimal supervision, as well as to coordinateing all aspects of CMC regulatory submissions relevant to their assigned projects or programs. This person will serve as the regulatory CMC representative on relevant biologic project teams, and as the reg...
This position is 100% in-house at HCRI in Boston, MA. The Clinical Trial Associate II is responsible and accountable for Study Start-Up (SSU) and country regulatory related activities, including collecting original and electronic documents, negotiate Informed Consent Forms(ICFs), review and approve site regulatory documents and ICFs, perform site identification activities. Create regulatory docum...
The Research Administrator/Senior Research Administrator is responsible for supporting faculty and staff throughout the life-cycle of a funded project, including guidance with proposal preparation, proposal review and submission, award review and negotiation, post award non-financial management and close-out of the project. The RA/SRA brings together a broad range of knowledge and experience in su...