(US-Massachusetts-Boston) Clinical Trials Statistical Programmer SAS programmer required for work on clinical trials team. Looking for at least 5 years of SAS experience, 5 years in a clinical trials environment in a Biotech or pharmaceutical environment- NOT in an academic/ research environment. Candidates MUST have the following: * 5 years experience with SAS * 5 years experience in a clinical trials environment * U.S. experience in a biotech or pharmaceutical environment * Ability to work independently Contract for 6 months to start, usually runs about a year. Client is located in Cambridge, MA. Initial phone screen to be followed by an in-person interview.
(US-Pennsylvania-Philadelphia) MJ Research, Inc. (MJR) is a leading biotechnology company specializing in the instrument and reagent technology needed for modern biological research. The company has grown from a small attic-based operation to a multinational corporation that is recognized worldwide as the industry leader in its field of technology. The company has facilities in Waltham & Watertown, MA; South San Francisco, CA; Reno, NV; Sauk City, WI; vaerlose, Denmark; Seoul, South Korea; and Beijing, China. Affiliated companies also have offices in Toronto, Canada and Tokyo Japan.
(US-California) SENIOR SAS CLINICAL PROGRAMMER for our client, a Bay Area biopharmaceutical company. DESCRIPTION The Sr. SAS Clinical Programmer will provide SAS programming leadership and collaborate cross functionally within the study team. S/he will plan, execute and validate SAS programming in support of clinical study reports for all phases of clinical studies, work with Clinical Team to formulate analysis data definitions, summary table, and listing specifications. Additionally, s/he will be responsible for the timely completion of SAS programming deliverables without compromising efficient use of I/O and CPU, developing and designing clinical programs, making recommendations for improvements, and implementing documentation and validation practices related to SAS programming per SOPs. Further responsibilities include participating in application development planning, design and support and providing technical guidance and mentoring to less experienced SAS programmers. QUALIFICATIONS The ideal candidate will have a Bachelors (advanced degree strongly preferred) in a relevant field complimented by a minimum of five years of SAS programming experience in a pharmaceutical/CRO clinical trials (Phases I-III) environment. S/he must be fluent in clinical data presentations style, statistical procedures and regulatory guidelines as well as be able to perform advanced techniques using SAS version 8.2 including BASE, GRAPH, STAT, the Macro facility and the ODS. Further requirements include strong analytic, critical thinking, oral and written communication skills. S/he must be detail oriented, highly motivated, able to take initiative, work well under pressure and shifting priorities, and work independently and as a team member. A working knowledge of SAS/IntrNet, CONNECT, SHARE, SQL, Oracle, and RDBMS is desirable. A good understanding of computers at system level and how SAS system configurations interact with the operating system and proficiency in UNIX and scripting is also preferred. COMPENSATION Compensation is competitive and includes a base salary between $85K-$100K as well as a comprehensive benefit package. Relocation is available for this position.
