eBay Classifieds  » Jobs » Biotech, R&D, & science » 1-17 of 17 ads for clinical research in San Francisco Bay Area

Title: Sr. Data Manager Company: Biotechnology Company Location: San Francisco Bay Area Status: Full-time Role: • In this role, the Senior Manager/AD will be responsible for managing the data management functions for all Sponsor clinical programs, including outsourced data management vendor/systems and will be responsible for oversight of CRO data management and ensure data compliance accordance with ICH/GCP. • This position is responsible for ensuring achievement of his/her own goals as ...

  Title: Sr. CRA Company: Pharmaceutical Location: San Francisco Role: • The Senior CRA is responsible for the implementation and management of assigned clinical studies, focusing on the areas of protocol development, study planning and conduct, site monitoring and/or monitoring management, enrollment and data quality, and adherence to corporate timelines and objectives. Responsibilities: • Ensures that clinical documents (i.e. protocols, ...

CRAs - Join Covance and receive an iPad AND a $5000 incentive!   You will be able to “spring” for your desires with our incentive!   Experienced Clinical Research Associates (CRAs)/Monitors: We are hiring for Late Stage (Phase II-IV) CRA positions. When you join Covance you will receive an iPad AND a $5000 hiring incentive.   Positions are home-based and needed throughout the United States.   All therapeutic areas needed.  Please let us know if you have clinical experience in cardiovascular ...

Regional Monitor/CRA (Portland, OR, Denver, CO, Iowa City/Nebraska, San Francisco):   Regional Monitors needed for positions across the U.S. The most urgent locations are: Portland, OR, Denver, CO, Iowa City/Nebraska, San Francisco, CA.    Qualifications include:   Must have a home office in the metropolitan areas (relocation not offered/provided). Will consider strong Coordinators, with a BS degree, proven Oncology monitoring/co-monitoring skills and experience along with HA submission, site ...

Provide strategic leadership for teams focused on the development of personalized medicine based on the discovery of molecular biomarkers. Utilizing patient derived data from genomic and molecular analyses you will develop strategies to identify new therapeutic targets. Shall: *** Establish internal collaborations with preclinical research and clinical science develop pre clinical plans to validate new pathways associated with drug response and translate findings into clinical practice *** ...

Qtech Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed as SAS programmer towards Clinical Research / Financial Banking / Risk / Credit / Healthcare Claims / Adjudication Analysts with clients. Training is required prior to the internship. Internship is provided for 3-6 months depending on the project and performance during initial training. The students will be selected and qualified for one of the career pathways for learning. ...

Qtech Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed as Business Analysts towards Clinical Research and Safety Reporting / Financial Risk and Credit Banking / Medical Healthcare Claim / Insurance and System Analyst with clients: Internship includes prior training, which follows real time experience and exercise learning pattern. Educational Qualifications: Bachelor Degree or Higher in Business Management / Computers / IT Only students ...

Seeking PhD, ability to design and conduct in vitro cell based assays, stem cell differentiation, and biochemical assays, and a history conducting muscle and biological fluid histological analysis to lead a team of scientific professionals performing: *** Development and execution of cell based assays to support mechanism of action and target validation studies. *** Biomarker discovery and translational studies to refine mechanistic understanding of molecular targets in chronic kidney disease. ...

 This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor: · Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements,  Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects · Conduct Pre-Study Site Visits (or calls), Study Initiation ...

Seeking leader with 10+ years in pre-clinical drug discovery and Ph.D. in cellular or molecular immunology or MD with training in respiratory, inflammation or autoimmune disorders and a track record of successfully moving drug leads through discovery process to clinical phase. Requirements: *** Track record managing operational budgets. *** Ability to recruit, lead and develop top rated scientists in a multi-task extremely fast-paced environment and constantly changing priorities. *** ...

 Clinical Operations Leader Responsible for coordinating the functional team members and their activities across all geographies, liaising with project leadership and the sponsor to ensure that the Global Research Operations deliverables (timeline, quality, productivity) are met. The ClinicalOperations Leader has overall accountability for the execution of the clinical operations strategy on the project. May act as Project Leader for projects involving a small number of services, where no Project ...

 -Provide consultation and advice in quantitative/statistical, experimental design and data management issues to support clinical, manufacturing, quality operations (quality control, validation, quality assurance), development (product and process development) and research for all diagnostics business areas. -Produce SAS® programming and other software package programming to support for clinical and nonclinical projects. -Produce statistical analyses and summaries and write formal memoranda. -Review ...

 The Senior Clinical Trial Manager (“CTM”) is responsible for managing the operational implementation of studies to support the development and commercialization of novel assays which lead to improved treatment decisions for oncology patients; and investigator and other collaborative studies to support the use of the commercial assays in facilitating treatment decisions for patients. The Senior CTM I is expected to provide functional expertise to, and project planning and management for study and ...

Hello,   My name is Francheska and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Senior Biostatistician for a prominent client of ours.  This position is located in South San Francisco, CA. Details for the positions are as follows:   Qualifications/Core Responsibilities: Contribute to clinical development projects, including study design and implementation topics, data analyses and CSR preparation.  Develops statistical programs as necessary to ...

We are in need of strong writers for a large CRO in the East Coast! Must have written all of the following: NDA submissions, Protocols, Narratives, Case Report Studies, and Inform Consent forms   Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final ...

The Clinical Research Scientist will be involved primarily with medical writing. Significant medical writing expertise and learning ability required to maintain pace in the market (MS Office: Word, Excel, PowerPoint). • Exceptional communication skills both oral and written. • Excellent problem solving ability. • Effective project and time management skills. • Excellent planning and organizational skills to demonstrate initiative. • Ability to demonstrate good business judgment. • Clinical trial ...

We are currently looking to hire Permanent Regional CRAs Job Description   The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification ...