Biotech Jobs in San Francisco, California

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181 San Francisco, CA Biotech jobs found on Monster.

Jobs 1 to 20 of 181
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Position Overview Independent principal investigator of projects responsible for overseeing all aspects of project delivery; delegates project management tasks to mid-level and junior staff. Takes scientific responsibility for project completion; responsible for strategic consultation and for use of best methods to address research needs. Oversees and participates in a large project portfolio. Inn...
Johnson & Johnson companies are equal opportunity employers. SENIOR DIRECTOR, CUSTOMER INNOVATION CENTER – CONSUMER-7977140626 Description The Johnson & Johnson (J&J) Innovation Center – San Francisco is recruiting for a Senior Director, Customer Innovation Center – Consumer, located in San Francisco, CA. Johnson & Johnson Consumer Group of Companies develops and markets consumer healthcare, baby...
* This team is an internal consulting team to other groups w/ data warehouses to help them learn and understand the data that they have at a new level re: BIG DATA when considering ALL of the data Client has and they need to try and predict behaviors based on all of the data they have and for other analysis. * The role they have on team are a result of BIG DATA. * JAVA, Hadoop, Pig, Hive, and have...
Worldwide Clinical Trials is a therapeutically focused global CRO that provides full-service drug development services to the pharmaceutical and biotechnology industries. As one of the most innovative and scientifically-driven contract research organizations, we offer exceptionally strong clinical trial methodology integrated with an effective global operations network. We are currently seeking hi...
This newly created position will audit clinical sites in this high profile QA organization. My client is a high growth pharmaceutical company with approved products as well as an outstanding pipeline. Qualified candidates can expect a base salary of 125,000 USD per annum. Information provided to Management Recruiters of Milwaukee West will be held in strict confidence. Advantages/Benefits: Ø Newly...
This newly created role will conduct and manage multiple GLP Compliance Audits on an ongoing basis within this highly visible QA group. My client is a high growth Pharmaceutical Company that can offer outstanding career growth and a fun work environment. Qualified candidates can expect a base salary of 125,000 USD per annum. Information provided to Management Recruiters of Milwaukee West will be h...
Job Number: 422071 Clinical Trial Manager / Sr. Clinical Trial Manager Primary Responsibilities and Duties: • Conducts and/or oversees all aspects required for selecting, initiating, monitoring and closing investigational sites in accordance with all applicable SOPs and GCP/ICH requirements. • Serves as a primary contact for internal study team members and external vendors and clinical sites. • Pr...
Senior SAS Programmer - Clinical Full Time Perm Excellent Pharma company in the San Francisco Bay Area has a terrific opportunity for a Senior SAS Programmer. Company currently working on three exciting new products including one that is nearing completion of its Phase 3 global trial. Several other new trials will begin in the next few months. Excellent salary and benefits. We will consider transf...
Job Number: 421886 Drug Safety Associate Description: The Drug Safety Associate will be responsible for the review, evaluation and management of adverse event reports from FG-4592, FG-3019, and other clinical trials in accordance with FDA, EMEA, CFDA, other applicable health authorities and ICH guidelines and regulations. The DSA will act as the primary Drug Safety representative for assigned stud...
An innovative and exciting pharmaceutical firm in the Bay Area is currently looking for a Director of Statistical Programming. The position holder would act as a lead throughout all SAS Programming tasks involved in clinical trial analysis and reporting. The following is a more detailed description of what this position will entail: Manage and lead assignments as well as programming personnel on m...
In support of technical transfer projects and implementation of internal quality system improvements and gap remediation, contractor to provide technical writing support associated with development and implementation of GMP documentation. Technical writer responsibilities are: Align with and execute this scope of work in accordance with project objectives, directives, and decisions Participate in...
Primary responsibilities include: Conducts and/or oversees all activities required for selecting, initiating, monitoring and closing investigational sites Serves as a primary contact for internal study team members and external vendors Provides oversight of CRO interactions in the areas of study/project management, monitoring, site management, trial master files, and data management Assists in the...
Our client in San Francisco is looking for a Scientist/Senior Scientist of Small Molecules to join their team! Scientist/ Senior Scientist of Small Molecules Duties: · Develop and optimize HPLC methods to report impurities and assay of small molecule drug substances and products · Develop, qualify, and validate methods and transfer of methods to QC for testing. · Work with contract laboratories. ·...
I have two Regulatory positions open with my clients in the SF Bay Area, a Sr. Regulatory Affairs Professional and a Regulatory Affairs Specialist, with many more opportunities to come in the near future! *These positions require that candidates be available to work 40 hours per week in a local office (There may be opportunities to work remotely 1-2 days per week after proven ability and level of...
• Provides fit testing and respirator training in support of the Respiratory Protection Program (60-70%) • Schedules and conducts environmental monitoring in the hospital including, but not limited to, bioaerosol and water sampling (10-15%) • Sample collection, packaging, chain of custody, possible lab delivery/drop off/coordination of courier (1-2%) • Supports the occupational monitoring program...
Our client in San Francisco is looking for a Regulatory Affairs Specialist to join their growing team! Duties: · Prepare regulatory documents or submissions for domestic or international projects. · Responsible for quality checking all submission documents. · Prepare routine regulatory correspondence, draft more complex correspondence, and assure submission to government agencies in support of inv...
Our client in San Francisco is looking for an Associate Director of Quality Assurance to join their growing team! Duties: · Review Drug Substance/Drug Product master and executed batch records · Review clinical packaging/labeling master and executed batch records · Manage CMO/CRO change control, deviation & CAPA systems · Conduct supplier audits · Maintain and improve quality systems · Test method...
Competitive Intelligence Marketing Manager - Biopharma, Healthcare, Contract SF Bay Area COMPETITIVE INTELLIGENCE MANAGER - Biopharma, Contract A biopharmaceutical leader is seeking two experienced Competitive Intelligence Managers to join the busy CI team on a long-term contract basis (temp-to-perm possible). The selected Competitive Intelligence Managers will begin in August, and contracts will...
Manager, Drug Safety Science Description Identify and assist in the management of safety concerns with the company’s drug product(s). Ensure that any safety signals are appropriately evaluated, communicated and managed with guidance from supervisor. Responsible for writing documents required for assessment & communication of product safety information for core safety documents. Telecommute option...

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