(US-California-Santa Barbara) Department Description: The department manufactures chemical intermediates and DNA for eSensor genotyping assays. Scope of Responsibilities/Expectations: The Manufacturing Specialist II is responsible for the production of intermediate reagents in compliance with cGMP requirements. The position requires demonstrated knowledge of organic synthesis and purification methodology. Manufacturing Specialist II exercises above average verbal, written and organizational skills and carries out his/her responsibilities using a background in chemistry sciences. Specific Knowledge: Organic chemistry sythesis, purification and analysis experience is required. Must be able to use computer controlled chemistry instrumentation, e.g. GC-MS, HPLC, Spectrophotometer etc. Must be trained in cGMP practices. Must be flexible and a quick study to adopt to the ever changing environment.
(US-California) SAS PROGRAMMER, Bay Area, CA, for our client, a global biotechnology company. POSITION DESCRIPTION The Senior SAS Programmer will work with Biostatisticians to provide SAS programming support in analyzing clinical trial results, generating report tables, listings and graphs for final reports. S/he will also design, develop, validate and maintain general use software applications and provide specialized programming support to the clinical project team and the data management group. QUALIFICATIONS The ideal candidate will have a B.S. or M.S. in Statistics, Computer Science, Life Sciences or other analytical science, complemented by at least two years experience in the analysis of clinical trial data, and strong SAS programming skills, including SAS macros. Experience with VMS, S-Plus, SAS/Internet, web design or Oracle is preferred. COMPENSATION Compensation is competitive and includes a base salary range of $60K-$78K and a comprehensive benefit package. Relocation is available for this position.
(US-Michigan) SENIOR MEDICAL WRITER, ANN ARBOR MI, for our client, a privately held Clinical Research Organization that enjoys a strong reputation in the industry. JOB DESCRIPTION The ideal candidate for this position will be responsible for the comprehensive statistical/medical document preparation process. The senior medical writer, an integral member of project teams, proactively supports the team and the initiatives of the company. The candidate will review and edit the works of other writers. Additionally S/he may also mentor and train other medical writers. This individual will also be responsible for team/project coordination or “technical leader” functions as they are assigned. QUALIFICATIONS To qualify for this position, the ideal candidate will have a life sciences degree (MS or PhD level preferably) complemented by five years experience in medical writing. S/he additionally should have worked on a minimum of four NDA/FDA Submissions. COMPENSATION A competitive base salary is open dependant on experience, and comprehensive benefits package is included. Relocation assistance will be provided.
