Biotech Associate Jobs

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1000+ Biotech Associate jobs found on Monster.

Jobs 1 to 20 of 3101
Needed: Manufacturing Associates & Data Entry Associates Kelly Services is currently recruiting Manufacturing Associates and Data Entry Associates to work within a well-established biotechnology company in Cambridge, MA. Successful candidates will possess a strong work ethic, ability to work independently, and a desire to grow in their career. These are long term, open ended contracts with HIGH 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...
Overview: The Business Analyst is an important member of C1 project teams and works closely with Consultants and Managers to solve interesting client problems, and to create and implement solutions. In this role you will own and personally deliver components of the client engagement, contributing to the overall success of each engagement. As you demonstrate strong analytic and project management ...
The Scientist position will perform a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical compounds in a variety of formulating. It has the same purpose and objective of the Associate Scientist position but differs in the level of expertise and supervision required. A Scientist is expected to possess a more thorough understanding of laboratory 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...
Description CSC has an immediate position for a Sr. Manager to support Dynport Vaccine Company (DVC). The Formulation Fill/Finish Senior Manager provides technical expertise to the DVC product teams and DVC subcontractors with regard to the formulation, fill and finish of DVC's products. The qualified candidate will design and implement testing plans for DVC biological candidates compliant with t...
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...
Description CSC has an immediate position for a Formulation/Fill/Finish Manager, supporting Dynport Vaccine Company (DVC). The Formulation/Fill/Finish Manager provides technical oversight of these activities to CMO subcontractors across vaccine development programs. This position is located in Frederick, Maryland. Essential Job Functions Provide leadership and technical expertise to the DVC prod...
Director, Marketing – Oncology Access & Reimbursements (Payer Marketing): My client, a well established biotech company situated outside of Boston, has multiple commercialized products and a solid pipeline. They are a company committed to growing their current therapeutic areas, as well as entering into new ones such as oncology, by developing both biotherapeutic proteins and small molecules. The...
Our client is a growing biotech in Newton seeking a junior administrative candidate in a temp-permanent capacity ASAP!! In this role you would be sitting at the front desk and responsible for answering phones, greeting visitors and scheduling conference rooms; however this is more dynamic than a typical receptionist position as it will also provide direct support to the Operations, Human Resources...
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...
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
DESCRIPTION Serves as primary contact point between the sponsor and the investigational site. A Site Manager is assigned to trial sites ensuring inspection readiness through compliance with the clinical research protocol, company's Standard Operating Procedures (SOP), codes of Good Clinical Practice (GCP), applicable regulations and guidelines from start-up through data-base lock. Responsibilitie...
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...
DOCS Global San Diego, CA
Associate Director, Biostatistics Summary: The Associate Director, Biostatistics works extensively with Clinical Data Management, Science Team Services, and other project team members to effectively communicate data findings to the data manager and project team, including client clinicians and statisticians. The successful candidate will have the ability to present statistical methodology and tri...
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, and Local Trial Managers in New Jersey, Pennsylvania and New York who have primary therapeutic experience in Oncology and Cardiology as well as other therapeutic areas. Experience working with multiple protocols is required. Candidates will be expected to cover sites in areas within the Northeast. Experience faci...
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 ...

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