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R & D Jobs in Canton, Massachusetts

782 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...
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...
Regulatory Affairs Manager One of the largest in vitro diagnostic companies in the world is looking for a Regulatory Affairs Manager. The company is a privately owned and works globally to develop, manufacture, and sell measurement technologies. Requirements: Advanced Degree in Sciences 10+ years’ experience in Regulatory Affairs and in medical devices or in vitro diagnostics Knowledge of FDA...
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 ...
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...
If you are a Senior Manager, CMC & Regulatory Affairs with CMC Biologics experience, please read on! Top Reasons to Work with Us 1. Join an award winning team of scientists! 2. Be part of changing the nature of cancer therapeutics. 3. Experience tremendous personal and professional growth. What You Will Be Doing The Senior Manager, CMC & Regulatory Affairs will be responsible for preparing C...
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...
We are looking for a talented, hands-on, biomedical/biomaterials engineer with industry experience in tissue allografts, biologics and/or biomaterials to support the expansion of existing product lines as well as the development of new products. The successful candidate will be responsible for managing a range of product development efforts from product concept through product design and developm...
FM Global is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000-size companies with engineering-based risk management and property insurance solutions. FM Global helps clients maintain continuity in their business operations by drawing upon state-of-the-art loss-prevention engineering and research; risk management skills and support services...
ESSENTIAL DUTIES AND RESPONSIBILITIES: This individual will review, evaluate, and investigate product complaints relative to the identity, quality, reliability, safety, and effectiveness of Company's products. The Analyst will provide technical expertise and assistance in handling/categorizing complaints to comply with current FDA and international reporting regulations. Duties also include com...
Senior Manager, Medical Writing Job Locations US-NJ-Hampton US-MA-Needham Overview: We are looking for a person to fill the role of Senior Manager, Medical Writing. The job will be based in either Hampton, NJ or Needham, MA. The Senior Manager will support Celldex’s clinical development programs through leading medical writing projects, generation of documents relevant to clinical research, a...
Senior Manager, Statistical Programming Overview: The Sr. Manager in Statistical Programming will lead multiple projects to support drug development under supervision of the Head of Statistical Programming. The position will provide the technical expertise to support the development and maintenance of standard programing process including SAS Macros, Programming Specs (ADaM), and validation proc...
SENIOR RESEARCH SCIENTISTS - 6-10 YEARS OF EXPERIENCE Cambridge Biomedical is seeking technically-skilled, Senior Research Scientists for our CRO group. Industryexperience in assay development and validation and strong background with immunoassays (ELISA, MSD, Luminex, cell-based assay) as well as qPCR and FLOW is required. The Research Scientist will collaborate with other scientists in implemen...
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...
The manager will oversee, direct and mentor a team of Research Administrators/Sr. Administrators and Award Analysts/Sr. Analysts (approximately 8 professionals) focused on service excellence, continuous improvement and compliance with policies, processes and regulations. Provides quality control over the work output of the unity by clarifying and enforcing standard operating procedures, staff acco...
Overview: The Study Coordinator will interface with Principal Investigator, Clinic and Center personnel in team effort to coordinate multiple concurrent clinical trials. This job entails direct management and oversight of several clinical trials. The candidate should possess working knowledge of good clinical practice and an understanding of the Code of Federal Regulations with regards to clinica...
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Be part of an exciting and well-established company that seeks to add to our talented team! Summary This new position, based in the Northeast will help us build a new service line to deliver testing, certification, repair and decontamination services for biosafety cabinets, fume hoods and USP 797 cleanrooms. We currently provide environmental services to various industries, including companies, ...
If you are a Laboratory Information Systems Manager with experience, please read on! Based in Natick, MA, we are well-established and highly profitable “healthy living" company. Due to growth, we are looking to hire a Laboratory Information Systems Manager to join the team. An outgoing, team first mentality is a must. Hands on experience are a must. If you love being hands on and working with a gr...