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u003cp u003e u003cstrong u003eAbout the Job u003c strong u003e u003c p u003e n u003cp u003eThe Senior Scientist Development Operations sits on the Companion Diagnostics CDx Development Operations Team and is..
u003cp u003eClinical Genomics Scientist II - 000068 for Foundation Medicine Inc in Cambridge MA Duties Leads studies that integrate appropriate clinical data with next generation sequencing output and applies statistical..
Overview nNew Higher Pay Rates nResponsibilities nEach individual performs those waived moderate or highly complex tests authorized by CLIA Bus Prof Code Section 1204 and must possess a degree of..
Job DescriptionnProclinical is currently recruiting for a Cell Culture Research Associate with a pharmaceutical company located in Cambridge, MA. Job Responsibilities: Write and maintain accurate, complete, and timely data in..
ROLE SUMMARY Standard biological experiments now easily generate enormous volumes of data which require specialized and sophisticated approaches in order to extract meaningful biological insights. The Bioinformatician will be accountable..
Job Descriptionrnrn rnrn rnrnOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today,..
Repare Therapeutics is a 2017 “Fierce 15” drug discovery company backed by tier-one strategic and institutional biotechnology investors ( http://www.reparerx.com ). Repare develops novel, precision oncology drugs that target specific..
u003cpu003eClinical Genomics Scientist II - 000068 for Foundation Medicine, Inc. in Cambridge, MA. Duties: Leads studies that integrate appropriate clinical data with next generation sequencing output, and applies statistical analysis...
Job DescriptionnJob DetailsAs a key member of the Quality Control team, the QC Scientist is responsible to ensure the methods are in an appropriate GMP status prior to GMP manufacturing..
Bristol-Myers Squibb is a global Biopharma company committed to a single mission: to discover, develop, and deliver innovative medicines focused on helping millions of patients around the world in disease..
Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and consumer health products, as well as animal health products. Today, we are building..
** Must be able to work onsite, M-F, no remote work ** **Must have Biology/Biochemistry/Biomedical/Chemistry background. NO IT or facility project management. Please do not submit unless they have that..
Research AssociatenDepartment Descriptionn:nnPurification Process Development (part of Sanofi R & D) is responsible for development, scale-up, transfer, and characterization of downstream processes for early and late stage clinical and commercial..
To monitor to ensure all documentation with respect to customer interactions (i.e. speaker programs, advisory boards, consulting agreements, investigator meetings) has been collected and stored in Ipsen's relevant document storage..
job description job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to..
OverviewnLocated in Boston and the surrounding communities, Dana-Farber Cancer Institute brings together world renowned clinicians, innovative researchers and dedicated professionals, allies in the common mission of conquering cancer, HIV/AIDS and..
Amgen is seeking a Sr. Project Manager to join our team and work from Amgen's Cambridge, MA campus. To learn more:The Sr Project Manager will be responsible for integrating and..
Job DescriptionnJob #: 1054680Regulatory Operations Specialist 1054680 Job Scope & Purpose: Our Waltham based client is seeking a regulatory operations specialist to join their growing team. The incumbent will be..
Description At Thrive, we are motivated to change the way people think about cancer. We challenge the status quo and are willing to think differently. Our curiosity drives us. There..
Position Summary: The Clinical Researcht Manager is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). This one is a Global Phase 1b pivotal..
ROLE SUMMARY The purpose of this role is to: To serve as Global Regulatory Portfolio Lead, responsible for a general portfolio of Internal Medicine Products Provide global strategic specific expertise..
OverviewnNew Higher Pay Rates!!nResponsibilitiesnEach individual performs those waived, moderate, or highly complex tests authorized by CLIA, Bus. & Prof. Code Section 1204, and must possess a degree of skill commensurate..
Job DescriptionnCSI Professional is actively seeking a Certified Medical Technologist for our client located in the Boston, MA metro. This is an exciting opportunity to join a leading provider of..
Job Location: Lexington, Massachusetts Duties: Work as part of an integrated research team focused on identifying and validating novel therapeutic agents that deliver cell-based therapies for treating cancer. Work independently..
Job DescriptionnProclinical is currently recruiting for a Regulatory Affairs Coordinator with a biotechnology company located in Cambridge, MA. This is a role with the opportunity to learn and develop within..