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Pharmaceutical Biotech Jobs in Massachusetts

682 jobs

One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. Since its founding in 1981, the company has introduced breakthrough treatments that have provided new hope for patients. The company's areas of focus are rare genetic diseases, multiple sclerosis, cardiovascular disease, and endocrinology. Genzyme...

Product Manager, Global MS (Pharma/Biotech)-70087209-53738JC Description One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. Since its founding in 1981, the company has introduced breakthrough treatments that have provided new hope for patients. The company's areas of focus are rare genetic disea...

Ascent Pharma is looking for a Home-based Sr. Clinical Data Manager! RESPONSIBILITIES: •Review protocols for proper data capture including Case Report Form design. Able to perform a thoroughly detailed review of CRF data requirements. •Designs CRFs and creates annotated CRF and CRF completion guidelines. •Develop a Data Management Plan that outlines CRF flow, data queries, manual checks, and d...

Ascent Pharma is seeking a Home-Based Sr Biostatistician! ***APPLY TODAY OR REFER A FRIEND! We offer a terrific referral bonus! Divna Rosenzweig/Sr. Clinical Development Recruiter (310) 933-4549 Please send resumes directly to ***** Job Description This position will perform management functions relating to the administrative and scientific activities of specific project w...

Report to the Planning and Resource Lead Biotech units R&D Procurement Business Partner (BP) for Neuroscience (co-located in Cambridge Ma. and Cambridge UK) and Waltham Sites. (approximately 50%) Delivering strategic sourcing & project initiatives across a broad range of R&D categories (approximately 50%) Position located in Waltham Ma or Cambridge Ma (either preferred), Gaithersburg, MD accept...

Report to the Planning and Resource Lead Biotech units R&D Procurement Business Partner (BP) for Neuroscience (co-located in Cambridge Ma. and Cambridge UK) and Waltham Sites. (approximately 50%) Delivering strategic sourcing & project initiatives across a broad range of R&D categories (approximately 50%) Position located in Waltham Ma or Cambridge Ma (either preferred), Gaithersburg, MD accept...

The PV Operations Leader will oversee all aspects of global individual case safety report (ICSR) collection, processing and reporting in accordance with applicable regulatory reporting requirements and company standard operating procedures (SOPs). Responsibilities Include: . Recruit, hire, train, manage and mentor a team of safety professionals responsible for processing, regulatory reporting an...

Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on rare diseases and multiple sclerosis, we are dedicated to making a pos...

Report to the Planning and Resource Lead Biotech units R&D Procurement Business Partner (BP) for Neuroscience (co-located in Cambridge Ma. and Cambridge UK) and Waltham Sites. (approximately 50%) Delivering strategic sourcing & project initiatives across a broad range of R&D categories (approximately 50%) Position located in Waltham Ma or Cambridge Ma (either preferred), Gaithersburg, MD accept...

100% remote! Sr. Medical Writer Writes/edits clinical regulatory and other supporting documents for assigned studies/indications, and manages the overall development and approval process. Critically analyzes, synthesizes, and presents complex information. Provides QC review support as needed. Other Skills and Qualifications: 4years experience in the medical/regulatory writing field in the phar...

About The Opportunity: Our client is a place where experience and integrity come together to advance the state of clinical development. They do this by improving the design and implementation of clinical trials through the innovative application of statistical science, operations research, and information technology. Their knowledge is available in the form of both software and services. This kno...

Contracting Manager MS (Biotech/Pharma)-75012754-60139JC Description Genzyme has pioneered the development and delivery of transformative therapies for patients affected by rare and debilitating diseases for over 30 years. We accomplish our goals through world-class research, collaboration with the global patient community, and with the compassion and commitment of our employees. With a focus on...

Clinical/Regulatory - Safety Review Specialist Cambridge, MA DESCRIPTION •Responsible for aggregate review and reporting of safety data from various sources in support of regulatory aggregate reporting requirements, as well as safety surveillance and risk management activities.•This includes:oCreation, coordination, preparation, and completion of aggregate safety reports (e.g.PSUR, PBRER, PADER...

About The Opportunity: Our client is a place where experience and integrity come together to advance the state of clinical development. They do this by improving the design and implementation of clinical trials through the innovative application of statistical science, operations research, and information technology. Their knowledge is available in the form of both software and services. This kno...

arge pharmaceutical company in greater Boston area has an immediate need for a contract based Clinical Statistician.Approved through late December 2015 with the option to be extended.Role is onsite.Details are as follows: Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials. Excellent oral and written communication skills. Attention and accuracy with detail...

This is a remote contract position for a great client.Clinical Operations Specialist will collect, accurately document, assess, code and process adverse event reports related to the marketed drug products monitored within the time frames established by the Department and in compliance with global regulatory requirements.In this role, the Specialist will serve as a primary contact point and recipie...

Description: The Clinical Writer partners with Subject Matter Experts, Medical Directors and clinical team to create clinical study related documents in accordance with ICH, regulatory authority, and/or company guidelines.Creates a variety of clinical documents necessary for all phases of clinical research by organizing, analyzing, and interpreting scientific and statistical data.May also assist ...

About The Opportunity: Our client is a place where experience and integrity come together to advance the state of clinical development. They do this by improving the design and implementation of clinical trials through the innovative application of statistical science, operations research, and information technology. Their knowledge is available in the form of both software and services. This kno...

We are currently seeking a Senior Medical Writer for one of our best clients.The Medical Writer will work in collaboration with the Manager of Medical Sciences to ensure that clinical as well as pre-clinical documents accurately and consistently present key clinical messages in accordance with program goals and regulatory requirements. The incumbent will assist in authoring investigators’ brochur...

Overview Are you articulate and driven to succeed? Do you have a passion for science, but don’t want to be locked in the lab or are curious about a different kind of career that blends business and science? Do you wish there was a direct correlation between your work effort and your compensation? Do you enjoy working with people and are a natural at building lasting relationships? Have you ever w...