Hi All,
Hope you are doing great today. I am Arthur with Clinovo. I believe you would be a good match for the below positions. Please check and revert with your Resume and Details so I shall contact you as soon as I can. If you are not interested, possibly you know someone in your network that would be? We are offering a referral fee for any successful referrals. I look forward to hearing back from you. Thanks for your time and interest. *Job: #01* *Job Title: Sr. SAS Programmer* *Position Type:* Contract *Duration: *12 Months *Location:* Berkeley, CA *Pay Rate:* $Open *Job Description:* *Essential Job Functions:* · Work with Client’s and contract Biostatisticians, Statistical Programmers, Clinical Data Managers, Clinical Research Associates, Medical Monitors, Drug Safety, and Regulatory Affairs to analyze and report clinical trial data. · Work with Data Management in the development and review of Case Report Forms (CRFs), edit check specifications, and design and validation of data transfer specifications. · Assist in development and review of in-house monitoring and study status reports. · Assist Biostatistics in the development of the statistical analysis plan (SAP) and programming specifications, assess data accuracy and consistency, review analysis dataset specifications, write and implement quality control plans, conduct statistical analyses, and produce tables, figures, and listings. · Determine programming needs for ad hoc clinical requests. · Review SAS versioning updates and recommend new programming approaches. · Normally receive little supervision. Determine methods and procedures on new assignments. Provide guidance and oversight to other staff. *Experience:* · 8+ years experience in biostatistics or applications programming within clinical research in the pharmaceutical, biotechnology, or CRO industry with a Bachelor’s degree or 5+ years related experience with a Master’s degree. · Demonstrated technical skills using SAS for programming and statistical analysis, as well as excellent knowledge of clinical trial design, EDC systems, specification development, and data submission standards (CDISC). *Education:* · Bachelor's or Master’s degree in biostatistics, computer programming, math, or a related field. · Other Knowledge and Skills Required: · Strong team player. Ability to work independently and in a multidisciplinary project team environment, including interactions with external vendors and CROs. Ability to represent statistical programming group at project team meetings. · Detail oriented and strong organizational skills. · Leadership skills as well as demonstrated clear and concise verbal and written communication skills. Strong ability to influence project teams and other individuals effectively and to take a leadership role on SAS matters. · Ability to skillfully manage competing priorities and projects. · Ability to follow SOPs, guidelines, and standards. · Dedication to quality and reliability in all work tasks. Self-motivation, eagerness to grow professionally and commitment to self-development. *Job: #02* *Job Title: Sr. SAS Programmer* *Position Type:* Contract *Duration: 6 - *12 Months *Location:* Palo Alto, CA *Pay Rate:* $Open *Job Description:* The Senior Statistical Programmer position is part of the Statistical Programming Group (within the Biostatistics Department), and is responsible for developing software programs for the analysis of biometric data in accordance to departmental SOPs and guidelines. *Essential Functions: * · Represent data analysis function in multi-disciplinary teamwork · May represent the biostatistics function independently in the assigned projects · Create, review, or approve programming plans and specifications at project and study level · Program, according to specifications, analysis datasets, tables, listings, and figures for phase I-IV clinical trials and publications · Review key study documents produced by other functions (e.g. CRFs, data management plans, SAPs, clinical study reports, etc.) · Contribute to RFPs for programming services from outsourcing vendors; Oversee work of outsourcing vendors at study level · Maintain efficient interfaces with internal and external customers and vendors with support of the collaborating statistician(s) · Must be able to work independently on multiple projects concurrently · Develop or assist in the development of procedures and/or software to transfer data from outside sources, such as CROs or clinical laboratories, to in-house systems · Support quality control of deliverables related to biostatistics · Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation. · Contribute to the creation and maintenance of department SOPs related to clinical data analysis. *Minimum Requirements: * · Bachelor’s Degree in Computer Science, Statistics, Mathematics, Life Sciences or other relevant scientific fields; Master’s Degree preferred · Minimum of 5 years of experience in developing programs for clinical trials using the SAS system; · Good Knowledge of statistics and drug development process · Excellent proficiency in programming with SAS · Experience working with CDISC SDTM and ADaM compliant data sets · Experience in pharmacokinetics/pharmacodynamics modeling a plus · Solid verbal and written communication skills. * Thanks & Regards,* *Arthur Cotton* *Lead Recruiter* *Clinovo Inc.,* *Phone: 866-994-3121 ext 105* *Email: arthur.cot...@clinovo.com <arthur.cot...@clinovo.com>* *Web: www.clinovo.com <http://www.clinovo.com/>* *Linkedin: https://www.linkedin.com/in/arthurcottonb <https://www.linkedin.com/in/arthurcottonb>* -- You received this message because you are subscribed to the Google Groups "USITCV" group. 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