Biotech Associate Jobs

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1000+ Biotech Associate jobs found on Monster.

Jobs 1 to 20 of 2829
Associate Director, Medical Information: Attractive and Growing Biotech Co., NY/NJ area Summary: Our client, an innovative and dynamic globally traded biotech company, has a newly created position for an Associate Director, Medical Information reporting directly to the VP of Medical Affairs. You will have the opportunity to work within a very dynamic and fast-paced organization and lead Medical I...
Summary: A company specializing in high level contract services management and biotechnology support to emerging companies in the field of cellular and biological therapeutics is seeking a Manufacturing Associate. Responsible for performing various manufacturing activities related to the start-up and GMP production of a number of novel cellular products. Including but not limited to; assisting in...
Our client, an emerging NC-based biotech that is performing breakthrough research in the field of regenerative medicine, is actively recruiting for a very sharp, detail-oriented and quality-oriented scientist, with some bkgd performing cell culture work in industry, to join its award-winning R&D team. Company is developing a highly anticipated portfolio of tissue-engineered products. This Researc...
Johnson & Johnson companies are equal opportunity employers. Oncology Sales Specialist (New Brunswick, NJ) - Janssen Biotech, Inc.-1246140806 Description Janssen Biotech, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Oncology Sales Specialist to support the New Brunswick, New Jersey territory. Janssen Biotech, Inc. is a leading biopharmaceutical company that p...
Johnson & Johnson companies are equal opportunity employers. District Manager, Oncology (Pacific North West) - Janssen Biotech, Inc.-9600140718 Description Janssen Biotech, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a District Manager, Oncology, to support the Pacific North West region. Janssen Biotech, Inc. is a leading biopharmaceutical company that provides...
SUMMARY Assist in monitoring and maintaining sufficient raw/intermediate, cleaning, gowning, and miscellaneous inventory levels to meet current and future manufacturing needs. Assist in maintaining control over inventory held in the GMP warehouse to ensure the safety, quality, and purity of materials intended for use during the manufacturing process. Assist in monitoring and maintaining final pro...
Sr. Director, Regulatory Affairs: Cutting-Edge & Rapidly Growing Global Biotech, NYC Metro Area Summary: Our client, an innovative and dynamic globally traded biotech company, is looking to hire an industry-experienced Sr. Director/Director, Regulatory Affairs reporting directly to the VP. This company is very stable and growing quickly, as they not only have an approved product but also a very e...
Thriving biotechnology company is currently looking to hire a polished and professional Executive Assistant to provide comprehensive support to the Business Development team. In this role, you will be responsible for managing a wide range of support functions including, but not limited to, preparing correspondence and memoranda; managing complex calendars including scheduling meetings, appointment...
Senior Manager, Regulatory Affairs, CMC: Attractive and Growing Biotech Co., NY/NJ area Summary: Our client, an innovative and dynamic globally traded biotech company, has a newly created position for a Senior Manager, Regulatory Affairs, CMC reporting directly to the VP of Regulatory Affairs. You will have the opportunity to work within a very dynamic and fast-paced organization and lead CMC eff...
Johnson & Johnson companies are equal opportunity employers. Oncology Sales Specialist (Springfield, OR) - Janssen Biotech, Inc.-1142141208 Description Janssen Biotech, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for an Oncology Sales Specialist to support the Eugene / Springfield (over to Bend) Oregon area. Janssen Biotech, Inc. is a leading biopharmaceutical comp...
Biotech Quality Assurance Specialistis needed for atwelve (12) month contractopportunity with Yoh's client located inMyerstown, PA. Top Skills You Should Possess: - Ability to successfully interpret and apply good manufacturing practices (cGMPs) in a production environment - Minimum one-year experience in a Quality Assurance role required in a cGMP production environment. What you'll Be Doing:...
Our client, an RTP area biotech that is performing breakthrough research in the field of regenerative medicine, is actively recruiting for a skilled and knowledgeable scientific leader, with particular expertise in cell biology, to assume a key role on its research and development team. Company is developing a portfolio of highly-anticipated tissue engineered products, primarily in the vascular s...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Regulatory Affairs Carson, CA; El Segundo, CA Full-Time $50,000 - $90,000 Apply Apply Regulatory Affairs Carson, CA; El Segundo, CA Full-Time $50,000 - $90,000 Apply Job Details If you are a Regulatory Affairs and Compliance Associate with 3+ years of submitting drug master files, please read on...
DOCS Global New York, NY
This position REQUIRES previous on-site monitoring experience! The clinical research associate monitors activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols. Review regulatory documents as required and prepare site visit reports. Responsible for multiple projects and must work both independently and in a team environment. May particip...
Core member of the Regulatory Affairs team, supports activities associated with the management of premarket development submissions to FDA and other regulatory authorities worldwide. Assists in the development of regulatory strategies and regulatory submissions (IND, CTA, BLA) during clinical phase development for stem cell therapy products. Responsibilities: • Provides regulatory assistance o...
Immediate opportunities available for experienced Regional Clinical Research Associates. Ideal candidates must demonstrate a minimum of 3-5 years of on-site monitoring experience having been employed by either a CRO, Pharma or Biotech company. We are seeking individuals experienced with in multi-therapeutic areas , Oncology or more complex disease/trials experience is a plus. Travel will be 25% wi...
Duke Clinical Research Institute Durham, NC
Occupational Summary: Perform routine and moderately complex on-site and in-house site assessments independently for clinical trials research. Perform complex on-site and in-house site assessments with direction. Use critical thinking skills to monitor sites' compliance with study, sponsor, organizational, and government guidelines. Collect, document, update, and report study information accordin...
DOCS Global is actively seeking Clinical Research Associates (CRAII), Regional, Lead, who have experience working with multiple protocols. Experience facilitating pre-study initiation process, orienting site personnel on protocols and procedures, compliance to FDA Regulations and managing site activities is a must. Desired therapies include Oncology for one position and Cardiovascular, Infectious ...
DOCS Global is actively seeking Clinical Research Associates (CRAII), Regional, Lead, and Local Trial Managers in Chicago who have primary therapeutic experience in Oncology and Cardiology as well as other therapeutic areas. Experience working with multiple protocols is required. Experience facilitating pre-study initiation process, orienting site personnel on protocols and procedures, compliance ...
Seeking a Regional CRA with experience in Oncology. Responsibilities include site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out $(window).load(function() { $('.flexslider').flexslider({ animation: "slide", touch: true, controlNav: false, pauseOnAction: true, pauseOnHover: true }); }); .powered-by-text{ /* color:#3...

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