Hi All, Hope you are doing great today.
I am Arthur with Clinovo. I believe you would be a good match for the below position. 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. *Title: Sr. SAS Progrommer* *No. of Positions: Multiple* *Location*: Berkeley, CA *Position Type*: *Contract* *Rate: $Open* *Job Description:* *Essential Job Functions:* · Work with Client 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. *Thanks & Regards,* *Arthur Cotton* *Lead Recruiter* *Clinovo Inc.,* *Phone: 866-994-3121 ext 105* *Email: [email protected] <[email protected]>* *Web: www.clinovo.com <http://www.clinovo.com/>* *Linkedin: **https://www.linkedin.com/in/arthurcottonb* <https://www.linkedin.com/in/arthurcottonb> The information contained in this message may be privileged and confidential. It is intended to be read only by the individual or entity to whom it is addressed or by their designee. If the reader of this message is not the intended recipient, you are on notice that any distribution of this message, in any form, is strictly prohibited. If you have received this message in error, please immediately notify the sender and delete or destroy any and all copies of this message. -- You received this message because you are subscribed to the Google Groups "Exact Match" group. To unsubscribe from this group and stop receiving emails from it, send an email to [email protected]. To post to this group, send email to [email protected]. Visit this group at https://groups.google.com/group/exact-match. For more options, visit https://groups.google.com/d/optout.
