R & D Jobs in Billerica, Massachusetts

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314 Billerica, MA R & D jobs found on Monster.

Jobs 1 to 20 of 314
Job Description : Essential Function Provide site management for observational/non-interventional research study sites in accordance with relevant SOPs, study specific procedures and regulations. Responsibility for protocol expertise with accountability for quality and timelines and the following activities: * Site identification and selection * Negotiation of site agreements and budgets * Co...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
Job Description : Key Accountabilities • Perform quality assurance checks on study images. • Validate and maintain imaging database including images and tracking and review results for assigned projects. • Ensure the site personnel have a good understanding of the protocol, the requirements of the study so that they can fulfill their obligations to complete their study accurately. • Perform e...
The ideal candidate will possess an academic background in physics, chemistry, or electrical engineering, with in-depth experience in physical and chemical principles and practices. In addition, he or she shall possess strong interdisciplinary skills in mechanics, pneumatics, thermodynamics, and materials science. The candidate should also have academic training and industry experience in trace ex...
Job Title: Clinical Documentation Specialist Position Responsibilities QC Review of pre-study and study documents, coding of administrative and regulatory documents, verification of documentation, and maintenance of document tracking system. Collaborating with CTM to determine and respond to issues in regulatory documentation. Creates study specific document checklists in collaboration with th...
QA/QC Specialist III Needed in Lexington, MA Every day, Kelly Services connects professionals with opportunities to advance their careers. We currently have a contract opportunity with a global leader in the biotechnology industry in Lexington, MA. OVERVIEW This position supports the execution of quality systems including the external audit program. This position is responsible for successful, ...
Synageva BioPharma Corp. JOB DESCRIPTION JOB TITLE Manager, Pharmacovigilance REPORTING RELATIONSHIP Senior Director, Pharmacovigilance DATE AVAILABLE Immediately LOCATION Lexington, MA RESPONSIBILITIES Position Overview The Manager, Pharmacovigilance is a seasoned expert in the preparation, analysis, and follow-up of adverse event reports, including preliminary regulatory assessment f...
Manager, Pharmacovigilance Great Pharmacovigilance Opportunity Boston Area We are looking for a seasoned Pharmacovigilance expert who will manage all PV activities for the specified product and or programs in this exciting, high-growth, late stage/early commercial biotech Boston based company. This person will collaborate and act as key product expert with Safety physicians on program activiti...
Kelly Scientific Resources (Kelly Services, Inc.) is currently seeking a highly motivated Regulatory Affairs professional with for a key role at one of our top clients in Andover, MA. As a Regulatory Affairs Project Manager placed with Kelly Scientific Resources, you will be reporting to the Director of Regulatory Affairs & Clinical Research Develop and responsible for regulatory strategies for a...
Senior Microbiologist Temp to Perm: 6 months contract and then converts Permanent Waltham MA Work in a fast paced environment executing, troubleshooting and developing micro biological test. Responsible for ensuring compliance with regulatory, industry standards and internal laboratory procedures and practices are followed. Key Job Activities: · Create, edit, and review reports for client ana...
Director, Regulatory Affairs PixarBio seeks a qualified, highly motivated individual to serve as Director, Regulatory Affairs to implement the company’s regulatory strategies for all products. The ideal candidate will provide technical and regulatory expertise to the product teams and in accordance with the current FDA guidelines. The position will report directly to the CEO. Our CEO has been ca...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
Job Description : Essential Function The Observational Research Leader has overall accountability for the execution of the clinical operations strategy on the observational study/registry. The Observational Research Leader is responsible for coordinating the clinical team members and their activities across all geographies, liaising with project leadership and the sponsor to ensure that the Obse...
Sr. Statistical Programmer The Senor Statistical Programmer provides technical expertise for the conduct of clinical trials, might act as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programming activities related to analysis and reporting. • Coordinate project start-up activities, including Unix/PME...
Purpose Manage the Investigator Sponsored Trial program across all product offerings, including all processes related to multiple functional areas. Responsible for the function and compliance of the Medical Information group to ensure accurate, appropriate and timely availability of medical information in full regulatory compliance to medical liaisons, clinical teams and senior management Essen...
Senior Scientist – Fermentation Process Development The Process Development Group provides support through the development and optimization of production processes. We work with our Strain Development team and manufacturing colleagues. We are seeking a Fermentation Scientist to join our Process Development team. Responsibilities include all aspects related to development of a robust and scalable ...
Dyax is a biopharmaceutical company focused on the development and commercialization of products for unmet medical needs while creating value for patients, employees and shareholders. We are driven by one unifying factor which is to improve the lives of patients. We currently market a product for the treatment of acute attacks of hereditary angioedema (HAE), a rare genetic disease. We also have an...
Dyax is a biopharmaceutical company focused on the development and commercialization of products for unmet medical needs while creating value for patients, employees and shareholders. We are driven by one unifying factor which is to improve the lives of patients. We currently market a product for the treatment of acute attacks of hereditary angioedema (HAE), a rare genetic disease. We also have an...
Dyax is a biopharmaceutical company focused on the development and commercialization of products for unmet medical needs while creating value for patients, employees and shareholders. We are driven by one unifying factor which is to improve the lives of patients. We currently market a product for the treatment of acute attacks of hereditary angioedema (HAE), a rare genetic disease. We also have an...
Laboratory Technician Responsibilities for Laboratory Technician: Sample processing and manual ELISA assay performance Operation and maintenance of automated analyzer Reagent preparation and inventory maintenance Requirements for Laboratory Technician: BS in Biology, Immunology, Medical Technology or related 2+ years of clinical laboratory experience 1+ years of manual ELISA experience Ex...

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