(US-California) Our client, a major pharmaceutical company in La Jolla, CA is looking for a Business Analyst with the following qualifications: Working in a project team to provide analysis for activities required to implement COTS and in-house developed solutions for use by various groups in PGRD. Responsibilities include: Developing and/or modifying business cases, use cases, requirements, process maps, test plans and protocols, procedures, user guides, migration plans, retirement plans and other project deliverables within the guidelines of departmental procedures. Other responsibilities include: attending/facilitating meetings and writing meeting minutes, providing status reports to the project manager, and to troubleshoot technical issues if needed. Qualifications: Successful candidate will have 3-5 years of business analysis experience. Must have extensive experience working with clients in a face-to-face environment, requirements generation, business interviewing, cost/benefit analysis, ROI, and strong presentation skills. The candidate must be self-motivated, independent, and collaborative, with a demonstrated client focus and service orientation, demonstrated effective organization and planning of time and resources. Attention to detail and the ability to function in a dynamic work environment are essential. Looking for a business/systems analyst with superior technical aptitude and an ability to understand architectures and systems analysis and design. Must have IT proficiency. Must have demonstrated skills in good documentation practices. Pharmaceutical experience and understanding of GXPs and computer system validation principles are a plus. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
(US-Connecticut) Our client, a major pharmaceutical company in New London, CT is looking for a Genetic Statistician with the following qualifications: The ideal candidate would have a working knowledge of population genetic analysis and posses excellent statistical and programming skills across several languages/packages (e.g. SAS, Splus, Perl). *** Please note the profile we are looking for is a Genetic Statistician NOT a SAS PROGRAMMER. Work with geneticists and clinicians to plan genetic association studies, typically of unrelated individuals. Do sample size and power calculations to assess utility of each planned study. Review clinical and genetic data for quality. Plan and execute all aspects of the statistical analysis of the study, and write a report summarizing the results. Work with genotyping laboratory to troubleshoot assay issues. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
(US-Illinois) For more than a century, our client has been working to advance health care for people around the world. They have evolved into a diversified health care company that discovers, develops, manufactures and markets innovative products and services that span the continuum of care from prevention and diagnosis to treatment and cure. They provide total integrated solutions across the health care spectrum for some of the worlds most prevalent medical conditions, including AIDS, cancer and diabetes. Our client, a major pharmaceutical company in Parsippany, NY is looking for a Clinical Application Specialist III -C with the following qualifications: Back-up contact for programming of tables, listings, and graphs for a specified compound project. Responsible for the validation and quality assurance of any output produced for specified projects and contributing to all project management such that timelines are met. Back-up participant on Clinical Project teams representing clinical programming efforts for that clinical team. Prefer candidate with clinical experience. SAS program experience required. A degree in statistics, computer science, mathematics or a related field B.S. or M.S. degree is preferred. Ph.D. would be a plus. 3 to 7 years of experience in the Pharmaceutical Industry - generating analysis, reports and graphs for individual studies and ISS, ISE; NDA submission to FDA. Knowledge of Windows NT 2000, UNIX operating systems & Programming knowledge of FORTRAN, C, C++, VISUAL BASIC or ORACLE/SQL would be desirable. Excellent programming skills in SAS is essential. Provide programming support to analyze clinical data, and generate reports and graphs on assigned projects. Analyze and construct logical database to facilitate programming for statistical reports and analysis, and provide consistency between records. Process programming requests to produce listings, tables and graphs for both safety and efficacy analysis. Ensure conformance to standard output, and avoid duplication of effort. Check output; identify and resolve database, data, logic or programming problems. Ensure accurate reporting; listings, tables and graphs reflect the database. Data is within expected range. Effectively manage deadlines or critical milestones on assigned projects. Design and develop various software and systems to effect generalized programming effort across projects. Improve productivity and efficiency; promote continuous improvement. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position.
(US-New Jersey) Our client, a major pharmaceutical company in Parsippany, NJ is looking for a Help Desk Level 1 Analyst with the following qualifications: Candidate must be proficient in Outlook 2000/2002. Also IE6.0 experience is required. Experience with Word, Excel, PowerPoint. Requires knowledge of IT operations, workflow processes and procedures to resolve inquiries independently. Basic troubleshooting (password log in issues, network connectivity, and printing problems). Ability to type 45 wpm. Strong analytical and communication skills and ability to work efficiently and effectively with clients, co-workers and other infrastructure systems staff. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
(US-Michigan-Ann Arbor) Our client, a major pharmaceutical company in Ann Arbor, MI is looking for a Statistical Programmer with the following qualifications: Requirement Notes: Candidates will have experience with clinical database, clinical research and clinical trials (operational knowledge). Also experience in Phase 1 - Experimental Medicine, Phase II - Proof of Concept, and Phase III - Full Development. An Associates Degree is preferred and 1 -2 years experience needed. You MUST meet all of the above qualifications in order to be considered for this position. You MUST be either a US Citizen or a Green Card Holder in order to be eligible for this position. Unfortunately, at this time we CANNOT work with third parties or relocate anyone.
(US-Massachusetts) Manage and lead a functionally oriented team focused on analytical method development and high throughput characterization of parallel synthesis products. RESPONSIBILITIES: 1)Manage a 13 member team (of BS, MS, PhDs) that provides method development capabilities to synthetic chemistry and maintains a HTP characterization operation. 2) Assure a high level of productivity and maintain the team on the cutting edge of high throughput characterization, responding to changing needs of external collaborations and analytical methods that become available. 3) Interact closely with peers from synthetic chemistry and parallel synthesis operations to assure an efficient process and productive work flow. Requirements: EXPERIENCE: PhD, ideally with a Post-Doc and at least 7-10 years industry experience or equivalent. A strong background in either separation science or mass spectroscopy, ideally with a PhD obtained in a recognized lab that specializes in either one PLUS Experience with quality control/characterization of small organic molecules.
(US-Massachusetts) Question: Are you looking for an opportunity to take responsibility for a clinical development program? If so Read on Responsibilities: Reporting to the CMO you will be charged with managing and driving all aspects of an oncology clinical development program. Responsible for all aspects of Phase 1-4 development including but not limited to site selection, protocol development, trial initiation, clinical regulatory submissions, monitoring oversight, and data analysis. Manage all aspects of external vendor contracts including CROs. In this position, you will assist in developing clinical trial protocols; manage, train, and mentor clinical trial managers; research, write, and edit clinical reports; work with internal and external stakeholders to design clinically sound development strategies; ensure completeness, accuracy and validity of clinical data; assure compliance with internal SOPs, FDA regulations and GCP; and participate in clinical regulatory submissions. Participation in regulatory submission including INDs, IND safety reports, BLAs, product labeling package inserts, and other reports as necessary. Manage all aspects of clinical program budget. Sound exciting?? Read on to see if you qualify! Qualifications: Masters degree (Ph.D. preferred) and 5+ years of clinical research and clinical program management experience in an industry setting. Oncology and biologics experience strongly preferred. Experience in developing clinical development plans (pivotal trial experience highly preferred), clinical trial design, protocol development, managing the writing of clinical sections of regulatory submissions, and management of industry-sponsored clinical trials required. Comprehensive knowledge of drug clinical development processes (Phase I III), policies, and regulations. Extensive CRO management experience required. Participation in preparation and management of major regulatory submissions.
(US-California-Silicon Valley/San Jose) Vitra Bioscience, a biotech company located in the Bay Area, is looking for a research scientist to join its cell biology group. The ideal candidate should have a Ph.D. in cell biology, or equivalent area, with 3 to 5 years experience in drug screening or drug development. Extensive knowledge of cell biology and experience in the development of cell-based assays is a must. Familiarity with image analysis systems and or microscopy is a big plus. Experience with data analysis and data visualization software packages is also a plus. We are looking for individuals with initiative, leadership qualities, and excellent written and verbal communication skills. Vitra offers full benefits, competitive salaries, and an excellent stock incentive plan.
