Clinical Dietitian jobs in the Biotech, R&D, Science category in Massachusetts

The Clinical Project Manager is responsible for independently managing multiple clinical trials of moderate complexity or managing a broader range of activities on large multi-center studies. The Clinical Project Manager is expected to address site and vendor related issues, with assistance as needed. Specific responsibilities include the clinical trial management of timelines, budgets, resources,...
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A health care company with global reach. A product pipeline filled to the brim. A team committed to scientific advancement. Think what's possible. A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented, performance driven people. All of which makes us one of the most rewardin...
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Job ID: 23354 Date Posted: 02/20/2013 Location: Galleria Job Family: Clinical Research Full/Part Time: Full-Time Regular/Temporary: Regular FLSA Status: Nonexempt Job Summary Located in Boston, Dana Farber Cancer Institute brings together world-renowned clinicians, innovative researchers, and dedicated professionals as allies in the common mission of conquering cancer, HIV/AIDS and related disease...
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EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany, a global pharmaceutical and chemical group. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, as well as oncology and autoimmune/inflammatory diseases as emerging ...
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TechData is hiring SAS Programmer (Some positions can be telecommute) and Biostatistician (Some can be telecommuting)for our pharmaceutical clients. Please see below requirements and send your resume to: dan.chen@techdataservice.com or recruiting@techdataservice.com. TechData is a leading provider for temporary and permanent positions in the pharmaceutical industry. TechData offers the best pay ra...
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Job Summary:Performs the coordination and preparation of document packages for regulatory submissions from all areas of company as well as internal audits and inspections. Compiles all materials required in submissions, license renewal and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking/...
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Theres quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, its a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Currently, we seek a Specimen Technician I for our Cambridge, MA Laboratory. Days and Hours: Tuesday - Satur...
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ORGANIZATION DESCRIPTION: EMD Serono is the biopharmaceutical division of Merck KGaA, Darmstadt, Germany, a global pharmaceutical and chemical group. We strive to create value and benefit patients by transforming medical science into breakthrough solutions in our core therapeutic areas of neurodegenerative diseases, fertility and metabolic endocrinology, as well as oncology and autoimmune/inflamma...
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. This role is key for medical supervision and medical management of clinical trials in the North American Region (US & Canada). The Medical Advisor (MA) is the medical link between Medical Operations (and/or Units/Customers) and (potential) investigators or experts/Key Opinion Leaders (KOL's) in North American Region. He/she should be the medical support in the territory for the studies he/she is...
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Responsibilities: Review the Triage incoming reports for initial assessment of seriousness, expectedness, causality, and reportability for reports from clinical trials and post marking sources in accordance with local work instructions, US FDA regulations, and international guidelines and regulations with high level of accuracy, accountability, and minimal supervision Assist with data entry of inc...
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Quality Assurance Auditor II Job Objectives and Tasks: Develops audit plans to ensure all clinical trials are conducted in compliance with the study protocol, site procedures, and all applicable regulatory requirements Conducts CQA audits of clinical sites, clinical quality systems, clinical vendors and regulatory documents to ensure clinical trials are conducted per Good Clinical Practice (GCP) r...
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ALEXION PHARMACEUTICALS POSITION SUMMARY Title: Senior Statistical Programmer Reports to: Senior Manager, Statistical Programming Location: Cambridge, MA Company Description Alexion Pharmaceuticals, Inc. is a biopharmaceutical company working to develop and deliver life-changing drug therapies for patients with serious and life-threatening medical conditions. Alexion is engaged in the discovery, d...
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Job Title: TMF Manager Position Description This position is responsible for management of Clinical and other sections of the Trail Master Files (TMF), utilizing records management best practices and appropriate technologies. The individual will provide leadership and expertise in records management and archiving support for clinical research work. Including the completeness, safekeeping and acces...
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Job Title: Inform Database Developer Position Responsibilities Plans, directs, and manages the clinical database design and maintenance process. Reviews the protocol and associated reference material and develops the database design project timeline. Maintains database design timelines. Promotes good project management practices. Conducts project initiation meetings with the database design team t...
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This position provides an opportunity to join a growing Drug Development Department and contribute substantially to the successful characterization, scale up, and manufacturing of novel CNS medications. In addition, there is an opportunity to expand your knowledge in the field of CNS research through day-to-day activities and close interactions with the Research and Clinical groups within EnVivo. ...
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We’re looking for an energetic, outgoing and detail oriented individual with a passion for improving how information is communicated in clinical trials. Acting as an extension of our client’s clinical trial operations group, you will use our novel technology platform to create and manage communication to clinical trial sites, motivating study team members to recruit and retain trial participants. ...
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Cambridge Biomedical, a specialized CRO and esoteric reference laboratory partnering with clients to provide Custom Solutions for Life Sciences Companies™ is seeking atechnically skilled and highly motivated Assistant Laboratory Supervisor to provide technical support to staff performing moderate to high complexity testing of esoteric assays. As a member of our team you will be responsible for: § ...
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Theres quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, its a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Currently, we seek a Specimen Technician I for our Cambridge, MA Laboratory. Days and Hours: Monday - Friday...
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BioBridges provides consulting expertise to help emerging pharmaceutical, biotechnology and medical device companies successfully span The Clinical Divide™. It offers its two services, ClinPath and ClinPoint for varying client situations and resourcing problems. By filling the voids in a company’s existing capabilities, BioBridges spans The Clinical Divide™. BioBridges ensures trials start off on ...
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Job Title: Regulatory Affairs Manager Position Description Serves as a liaison between the company and regulatory agencies for all assigned projects and is responsible for day to day regulatory support. Expected to provide guidance within Regulatory Affairs and to data generating departments to ensure timely filing and approval/maintenance of assigned programs. Position Responsibilities Responsibl...
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Diamond Diagnostics, is a manufacturer and international supplier of diagnostics laboratory equipment and supplies. The company is based in Holliston, Massachusetts and services clients in over 100 countries worldwide. Diamond is a fast-paced, dynamic organization seeking professional, enthusiastic, focused and skill proficient employees in the above mentioned capacity. The position entails the fo...
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Senior Project Manager Location: East Coast My client is a global leader providing enterprise software and services into the Life Sciences industry. They are a best of breed/niche player in the service offering and software products that sell into pharma/biotech. This is a large stable organization that’s experiencing growth and looking for a key executive to take them to the next level (50+m). If...
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Posting Title : FIELD RESEARCHER - Friedman School of Nutrition Science & Policy Requisition Number : 1862 City : Sierra Leone State/Province : Freetown Zip code : 00000 Job Description-Overview : *This is a grant funded, limited appointment position, with the possibility of extension for up to three years.* Position to start immediately and be located in Boston, MA, USA for approximately 2 months...
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The Role and your Responsibilities Project management support involving the building and maintenance of detailed dossier compilation and submission plans. Leads the development and implementation of regional strategy for timely periodic review and updates and implementation of appropriate Standard Operating Procedures (SOPs) within Regional Regulatory Affairs. Partner with other departments intera...
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One Year Benefit Eligible Assignment Associates of Cape Cod, Inc., a biotechnology company specializing in the detection of elicitor's of innate immunity is currently looking for an individual with a M.Sc. or Ph.D for a one year benefit eligible assignment. The successful candidate should have an interest in clinical applications of newly developed detection methods and a degree of expertise in Mi...
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