Face to Face Interview # SAS Clinical # Woodcliff Lake NJ
*Hi * *I Hope you are doing great today.* *Let me know if you are interested in below requirement.* *Please send the suitable resume along with Contact Details, Current Location as soon as possible to hve...@tekshapers.com <hve...@tekshapers.com> * *Position – SAS Clinical * *Location – Woodcliff Lake NJ* *Duration – 12+ months* *Interview process: Phone, then face to face* *Qualifications: * *• Strong knowledge of JReview and SAS programming skills required in Windows and UNIX environment, with proficiency in Programming in JReview, Graph, Dashboard, SAS/Base, SAS Macros, SAS Graph, SAS/AF/SQL. * *• 7-10 years of experience in programming with clinical trial data and preparing programming and test documentation. * *• Extensive experience of handling external data, such as lab data, PK, and imaging data. * *• Experience of developing programs using JReview. * *• Good understanding of standards specific to clinical trials such as CDISC, SDTM, MedDRA, WHODRUG. * *• Good understanding of relational databases such as ORACLE, Knowledge of the EDC system, InForm, and underlying data structure is a plus. * *• Knowledge of data management process, good understanding of data cleaning process. * *• Strong problem solving skills * *• Able to work independently and a team player, good organizational and time management skills. * *• Capable of communicating technical concepts * *• Good understanding of system development life cycles, GCP, and related regulatory guidelines.* * • Perform SAS programming to provide data review complex listings/reports to support Data Management, Medical Coding, and other areas of Clinical functions for Oncology trials. * *• Develop programs & graphs in JReview for easier data review and visualization. * *• Develop programs for patient profiles and ad hoc reports to support the clinical teams for Oncology trials. * *• Design and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the Oncology Data Management and other areas of Clinical for data review. * *• Develop and maintain the programs/tools including testing and organizing the SAS datasets, SAS programs and related documentation. * *• Ensure all programming activities and processes performed are conducted according to standard operating procedures and good programming skills. * *Regards,* *Himanshu Verma * *Talent Acquisition Executive* *[image: cid:image001.png@01D01011.0B0A3090]* *(W) **248-565-4747*172**; Fax: +1-248.254.7211* *Email: **hve...@tekshapers.com* <achau...@tekshapers.com> *Gtalk: **vermarecruiter* *Tekshapers Inc* -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at https://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
Hiring: SAS Clinical Manager 9 + years Experience ::: San Francisco, CA - California
Dear Partners/Job Seekers,We have a Corp to Corp opening for the following position. If you have matching candidates please submit their profiles. Profiles matching the below job requirement will be contacted at the earliest. Job Title : Hiring: SAS Clinical Manager 9 + years Experience ::: San Francisco, CA Location : California Key Skills : SAS, SAS Clinical Manager Experience : 9 YearsClick the below link to View and Apply for this Job.http://bighotlist.com/#/details/12081Thanks & Regards,KrishnaAASolLog in to www.bighotlist.com to check the complete job details. Connect with over 10,000 Staffing Vendors. Live! -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at https://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
SAS Clinical Manager - California
Dear Partners/Job Seekers,We have a Corp to Corp opening for the following position. If you have matching candidates please submit their profiles. Profiles matching the below job requirement will be contacted at the earliest. Job Title : SAS Clinical Manager Location : California Key Skills : Must have led studies as an FTE oncology & CNS experience hands on CDISC mapping experience Experience : 9 YearsClick the below link to View and Apply for this Job.http://bighotlist.com/#/details/12079Thanks & Regards,shashiaasolutionsinc.comLog in to www.bighotlist.com to check the complete job details. Connect with over 10,000 Staffing Vendors. Live! -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at https://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
Hiring for SAS Clinical Developer for Hampton, NJ | Need Locals Only | GC,USC Only
Hi Please lookup the below position and if you feel comfortable ,then please send me your updated resume *Position : SAS Clinical Developer* *Location : Hampton, NJ * *Duration : 6-12 Months Interview : Face to Face (within one hour drive for F2F interview & long-term employment. Some areas of NJ, DE, & PA are within range)* *GC , USC Only* * ** A background check and drug screen required if hired ** Need Very Good English Communication Skills*** *Job Requirement* · IT - 6+ years · SAS Programming - 5+ years · CDISC - 2+ years · ISS/ISE - 2+ years · Clinical / Pharma - 4+ years (Needs To Be Recent) · Ideal Candidate will have a background primarily from Pharma *Job Responsibilities* · Generate and validate tables, listings, and figures per protocol and statistical analysis plan and for ad-hoc requests. · Generate and validate SAS datasets using Clinical Data Interchange Standards Consortium (CDISC) standards. · Perform programming crosschecks of other programmer's work, including tables, listings, figures, and datasets. · Participating in the development of statistical analysis plan table, listing, and figure shells. · Perform program documentation on all programs, files and variables for future reference. Regards Sandeep Chauhan Technical Recruiter VSG Business Solutions 221, Cornwell Dr, Bear, DE 19701 Contact No.: 302-261-3207 X 103 Email: sandee...@vsgbusinesssolutions.com -- You received this message because you are subscribed to the Google Groups "Citrix and Sap problems" group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at https://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
SpotFire Developer :: With SAS Clinical Exp
Job Title: SpotFire Developer Location: Philadelphia , US Duration: 6+ Months Skills : Strong hand at SpotFire with clinical domain knowledge *JOB RESPONSIBILITIES*: Ø The ideal candidate will have a background in clinical programming in a data management setting or statistical setting. Ø Raising the request to setup the study id in spotfire file share area. Ø Adding the workflows using the Study Configuration tool. Ø Creating the Data visualization using the codes placed in spotfire file share area. Ø Embedding the study dataset into the workflow. Ø Open the workflow using Spotfire (via citrix). Modify the data visualization as per check requirement. Ø Creating the Study Specific Data visualization based on specification. Ø The ability to focus on customer needs, troubleshooting, and providing innovative technical solutions, while adhering to standards is essential. Ø This is a dynamic position that will require the successful candidate to learn a number of bespoke systems and solutions and implement those effectively in order to deliver a top-notch conversion service. ü Project management ü Communication ü Data management understanding ü Good SAS programming skills *Additional Activities:* · Support multiple functional groups (i.e. DM, SP, etc) across all phases · Lead and actively participate in review of Spotfire deliverables · Create Maintain process documentation as required · Lead or participate in process redesign optimization · SAS programming for creation / review of Spotfire domains as required · Training of new staff on the role · Provide training/guidance on Spotfire process for teams · Provide oversight to offshore team *Additional preferred skills:* · Experience extracting and transforming clinical data · Knowledge of clinical trial processes and supporting systems · Strong skills in SQL, PL/SQL. · Knowledge of FDA requirements for annotated CRFs · Experience with eDC/eDM setup for clinical trials *QUALIFICATIONS SKILLS:* Ø Bachelors’ degree in a scientific / technical discipline. Ø Programming Knowledge:SQL, PL/SQL, COGNOS, C# Ø Effective communication skills. (Verbal and Written). Ø 4+ years of experience in SAS and SpotFire programming (Pharmaceutical Industry) and familiarity with CDMS is desirable. Ø Ability to work across different platforms like VB, UNIX, and remote data capture technology is preferred. *BEHAVOIURS/ COMPETENCIES*: Ø Ability to speak to non-technical audience with assertiveness. Ø Knowledge of Quality control and Quality assurance. Ø Time management skills. Ø Collaboration and team work Ø Knowledge of regulatory requirements for electronic submission. Ø Assertiveness in explaining issues and ability to make recommendations. *Thanks Regards* *Hemendra Kumar* Insigma Inc | 1920 Association Drive Suite # 302, Reston, VA 20191 Phone: 703-468-3024 I Email: hemendra.ku...@insigmainc.com ABOUT THIS E-MAIL: The information transmitted is intended only for the person or entity to which it is addressed and may contain confidential and/or privileged material. Any review, retransmission, dissemination or other use of, or taking of any action in reliance upon, this information by persons or entities other than the intended recipient is prohibited. If you received this in error, please contact the sender and delete the material from any computer. -- You received this message because you are subscribed to the Google Groups Citrix and Sap problems group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at http://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
SAS Clinical Programmer required local to MA
Hello , Hope you are doing great Below find the job description If interested than kindly share your updated resume. *REQUIREMENT DETAILS:* *Net2Source, Inc. is one of the fastest growing IT Consulting company across USA. N2S is headquartered at NJ, USA with its branch offices in Asia Pacific Region. N2S offers a wide gamut of consulting solutions customized to client needs including staffing, training and technology. * *Job Summary: * *Company: *Net2Source, Inc *Job Title:* SAS Programmer *Location:* Boston, MA *Contract:* till 6/30/15 (extension likely) *Pay Rate:* $35/hr *Interview Mode: *Phone Screen (1) + In-person (1) LOCAL CANDIDATES ONLY PLEASE *Qualifications* *o **Knowledge of SAS* *o **Experience working with large datasets* *o **Proficient in Oracle SQL * *o **2+ years of experience with SAS Programming in a healthcare environment* *About Net2Source, Inc.* Net2Source is an employer-of-choice for over 1000 consultants across the globe. We recruit top-notch talent for over 40 Fortune and Government clients coast-to-coast across the U.S. We are one of the fastest-growing companies in the U.S. and this may be your opportunity to join us! *Want to read more about Net2Source? , *Visit us at www.net2source.com *Thanks Regards,* *Swati Pandit* *Net2Source, Inc.* *One Evertrust Plaza, Suite # 305* *Jersey City, NJ - 07302, USA* *Email:swati.pan...@net2source.com email%3aswati.pan...@net2source.com* *Office: 201.340.8700 Ext: 506* *GtalkYM: svsswati8* *Website : www.net2source.com http://www.net2source.com* -- You received this message because you are subscribed to the Google Groups Citrix and Sap problems group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at http://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
SAS Clinical required local to NJ
Hello, Hope you are doing good... Please Find the below requirement for your reference, if you feel interested please reply with updated resume. *REQUIREMENT DETAILS:* *Position: SAS PROGRAMMER (Clinical)* *Location: Woodcliff, NJ* *Duration: 12 months +* *Interview: Phone In-person* *Rate: $55-60/hr* *Responsibilities* - Responsible for SDTM data creation and delivery for oncology studies. - Prepare SDTM Mapping specification following company standards. - Create or participate in SDTM annotation for CRFs/eCRFs for oncology trials. - Develop programs to create SDTM datasets and Define.xml for statistical analysis, tables listings, and regulatory submissions. - Perform Open CDISC validation, coordinate to resolve issues, prepare associated documentation. - Design and develop SAS macros, applications, and other utilities to expedite SAS programming activities and usage by the Oncology Data Management and other areas of Clinical for data review. - Ensure all programming activities and processes performed are conducted according to standard operating procedures, good programming practices, and GCP guidelines. *Qualifications* - BS or MS in Computer Science or related field. - Five to Seven years of strong experience in programming with clinical trial data and developing programs, testing, and documentation - Strong SAS programming skills required in Windows and UNIX environment, with proficiency in SAS/Base, SAS Macros, SAS/Graph, SQL. - Extensive experience of handling SDTM mapping, related data structures, and programming to create SDTM data sets. - Extensive experience in SDTM validation using OpenCDisc. - Good knowledge in developing Define.xml and validation. - Extensive experience of handling external data, e.g., laboratory data, PK, ECG, Biomarker, Imaging, etc. - Good understanding of standards specific to clinical trials, such as CDISC, SDTM, MedDRA, WHO DRUG. - Good understanding of relational databases, e.g., ORACLE; Knowledge of the EDC System, InForm and underlying data structure is a plus. - Knowledge of using JReview/IReview is a plus. - Strong problem-solving skills. - Able to work independently and as a team player; Good organizational, time management, and project management skills. - Capable of communicating technical concepts. - Good understanding of system development life cycles, GCP, and related Regulatory guidelines. - Should be able to manage the assigned projects independently with minimum supervision. *Thanks Regards* *Swati Pandit* *Technical Recruiter* *Sage Group Consulting, Inc* *W:+ 732-767-0010 x 504 |Email: **span...@sagetl.com* r...@sageci.com *Gtalk: svsswa...@gmail.com svsswa...@gmail.com* *Yahoo: svsswa...@yahoo.com svsswa...@yahoo.com* *www.sageci.com http://www.sageci.com* [image: Description: saplogoone][image: SageLogoC] This message contains information that may be privileged or confidential and is the property of Sage Group Consulting, Inc. It is intended only for the person to whom it is addressed. If you are not the intended recipient, you are not authorized to read, print, retain copy, disseminate, distribute, or use this message or any part thereof. If you receive this message in error, please notify the sender immediately and delete all copies of this message. Sage Group Consulting, Inc does not accept any liability for virus infected mails. -- You received this message because you are subscribed to the Google Groups Citrix and Sap problems group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at http://groups.google.com/group/citrix-and-sap-problems. For more options, visit https://groups.google.com/d/optout.
Very urgent requirement : : SAS Clinical Programmer - NJ/MA/CA/IL - Long Term Roles
Hello, Hope you are doing good! This is very urgent opening. Please send your available matching candidates on ke...@riderconsultinginc.com I have wonderful opportunities for SAS Professionals. We have 4 locations NJ/MA/CA/ILbut we need candidates only with linked in profiles. Please share resumes only of the candidates who has an up to date linked in profile. Also mention that you are applying for which role and what location. Share your resumes accordingly. 1.Title: SAS Statistical Programmer Location: Boston MA Years of Experience: 7-10 Years Duration: 1.5 year contract Job Description The Statistical Programming Contractor supports statistical programming activities in the production of the analysis datasets, tables, listings, figures, electronic submission components, and complex ad hoc analyses. Depending on experience level, may lead a study. Responsibilities: • Does both production and QC programming of SDTM datasets, analysis datasets, tables, listings, and figures, for multiple clinical trials using SAS software. • Ensures standards at a drug program level; integrates data across multiple studies or drug programs. • Works with minimal supervision under the direction of a lead programmer. • Communicates issues to lead programmer or manager. • Must meet timelines or communicate proactively and effectively if timelines are at risk so that plans can be adjusted. • Expected to contribute to departmental process improvement initiatives. General Knowledge and Skills: • Able to handle a moderate to large volume of complex tasks with minimal supervision. • Able to handle ad-hoc requests with minimal guidance. • Recognizes when negotiating skills are needed and seeks assistance when necessary. • Excellent organizational, interpersonal, and communication skills. Minimum Educational and Experience Requirements: • Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Mathematics, Economics, Computer Science, IT, Biology, Social Science, etc. • Previous SAS programming experience, including SAS STAT, GRAPH and MACRO. • Previous relevant pharmaceutical/biotech industry experience. • Extensive knowledge of drug development process and clinical trials. • Extensive knowledge of drug submission requirements, relevant ICH and FDA/EMEA guidelines, CDISC standards. • Open to all levels ranging from 3 to 10 years of pharmaceutical/biotech industry experience 2.Title: Lead SAS Consultant Location: New Jersey Years of Experience: 7-10 Years Duration: 1 year contract Skills/Knowledge Required: • BA/BS degree in life science, statistics, mathematics, computer science, or related field OR equivalent working experience required. • 7-10 years Pharmaceutical/CRO experience as a SAS programmer supporting clinical trials for regulatory submissions. • Demonstrated knowledge in programming environments, systems and networking as it relates to the pharmaceutical industry. • Have in-depth understanding of clinical data structure as well as relational databases • Demonstrated proficiency in using SAS • Demonstrated skills in using software tools and applications, e.g., MS office, XML, HTML, etc. • Have an understanding of regulatory requirements pertaining to technology, systems, and standards. • Ability to research new technologies and ensure alignment with regulatory agencies and industry standards • Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM. • Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission. • Demonstrated ability to work in a team environment with clinical team members. • Excellent planning and project management skills. • Good interpersonal, communication, writing and organizational skills. 3.Title: Sr. SAS Programmer Location: San Francisco LA, CA Years of Experience: 8+ Years Length of Contract: 1 Year Desired skills and expertise: . Create SAS programs for data mining . Gather study team requirements and translate them into technical specifications for SAS programs . Program SAS data validation checks and listings to identify data discrepancies . Program SAS checks to integrate and reconcile data from external sources (including serious adverse events (SAE), lab results, ECGs, electronic patient records, medical devices and interactive voice response (IVR)) into the primary clinical database SAS datasets . Review Case Report Forms and formatting of SAS datasets extracts for accuracy and consistency . Provide programming support for Annual Safety Reports and Publications . Build standard SAS Macro library . Mentor junior level SAS programmers, if needed . MUST have prior FDA submission experience. . MUST have Oncology clinical trials . Bachelors Degree in related area . Minimum of 8+ years of SAS programming
SAS Clinical Programmers needed skype to hire in PA, NC, KS
Hi, Hope you are doing great. Please review the below requirement and mail back to *prad...@sriveninfosys.net prad...@sriveninfosys.net* *Title : 3 SAS Clinical Programmers* *Client : PRG* *Duration : 6+ months* *Locations : Multiple – Horsham PA, Raliegh NC Kansas City KS* *Required Skills:* · Employees at this level are required to perform all tasks associated with a Clinical Programmer and apply a breadth of industry and technical experience and expertise to lead multiple studies and/or integration projects. Additional duties include the following: · Provide leadership and oversight to programs of clinical trials and/or complex clinical trial projects, handling the related technical issues to ensure standard processes are implemented and overall consistency and quality is achieved. Work may include: · Serving as primary functional representative, providing input for clinical programming projects; · Overseeing and coordinating with leads/subleads for the individual trials or components of the project · Mentoring clinical programmers within a project team; · Serving as a resource for, and interacting with, other functional areas to facilitate project timelines; · Integrated database design, documentation and implementation; · Identifying and quantifying changes in scope. · Contribute to interactions with clients and vendors, such as the following: · Bid defense activities · Development and implementation of client/vendor standards · Evaluation of vendors for preferred provider relationships. · Share experience and expertise with internal and external colleagues: · Present department training; · Present at conferences; · Mentor clinical programmers in all clinical programming responsibilities; · Expand and maintain wiki. · Provide input into technical initiatives in order to develop and improve the standard processes within Clinical Programming. Work may include: · Serving as a functional representative, providing input for clinical programming initiatives; Applies knowledge of policies and procedures. Applies knowledge of computerized information systems and standard application software (Windows, MS Office). Excellent written and oral communication. Applies a basic knowledge of Clinical Programming. Applies basic knowledge of programming language, or other software languages/ tools as required. Applies attention to detail. Identifies programming and data issues and seeks guidance on resolution from higher levels. Follows established procedures as outlined in trial specific documents, SOPs and related work instructions. Uses existing techniques to perform accurate and efficient Clinical Programming. Errors can be easily and quickly detected within the immediate work unit and would result in only minor disruption or expense to correct. Close supervision involving detailed instructions and frequent monitoring of work performance. Contacts are primarily within the assigned clinical programming project teams and functional management. Tasks are expected to be learned by peer training, formal training, review of SOPs, related work instructions and trial specific documentation. Follows processes and specifications for the project, clearly communicating questions to Lead CP, mentor or functional management. *Other skills:* · Interact with biostatisticians, pharmacokineticists, medical writers, clinical systems developers, and other operations staff. · Produce figures and documentation of datasets, including define.xml files to support the tabulation and analysis of clinical trials. · Liaise with external data vendors (e.g. central laboratories, ECG vendors) to ensure that data is transmitted in required format. · Apply knowledge of the CDISC Standards, SDTM and ADaM. · Create derived datasets in accordance with derived dataset specifications. · Understand project budgets for clinical programming tasks and communicate potential issues to the project lead and/or functional manager. · Achieve utilization targets. *Thanks Regards* *Pradeep Kumar* *Technical Recruiter* *Sriven Infosys Inc* *Direct: 718-502-9128* *Email: **prad...@sriveninfosys.net* prad...@sriveninfosys.net* | Gtalk: pradeepkumar.sriveninfosys* *URL: *www.sriveninfosys.net -- You received this message because you are subscribed to the Google Groups Citrix and Sap problems group. To unsubscribe from this group and stop receiving emails from it, send an email to citrix-and-sap-problems+unsubscr...@googlegroups.com. To post to this group, send email to citrix-and-sap-problems@googlegroups.com. Visit this group at http
Need SAS CLINICAL TRIAL CONSULTANT in SF, CA
*REPLY TO: nagender.bon...@adventglobal.com* *Hi Partner,* *Please find the below job details and let me know if you have any suitable candidate?* SAS Clinical Trial Consultants – SF CA (Will hire off of phone interview) Position Duration: Client is looking for 5 folks to get them through Dec, scale down to 3 going into Jan and 2 in Feb. Strong possibility for additional work. Location: San Francisco, CA (Phone screen and would hire off the phone.) Start: ASAP Openings: 5 RATE: Max 40/hr on Corp-Corp 1-2+ years of SAS clinical trial experience. SAS® Clinical Data Integration Best Regards Nagender Advent Global Solutions, Inc 6 E. College Drive Arlington Heights, IL -60004 Phone: 847-849-1675 (D) Fax: 832.565.1418 nagender.bon...@adventglobal.com www.adventglobal.com -- You received this message because you are subscribed to the Google Groups Citrix and Sap problems group. To post to this group, send email to citrix-and-sap-probl...@googlegroups.com. To unsubscribe from this group, send email to citrix-and-sap-problems+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/citrix-and-sap-problems?hl=en.
SAS clinical
Hi, We have an urgent requirement with our client. Below is the job description, if you are available and interested, please send there profile to j...@tekatlantis.com along with the following information below. Visa Status- Location – Availability – Willing to relocate (Y/N)- Expected rate - This is another requirement. Find some SAS clinical guy in CA and we will have sureshot placement. 5 year healthcare SAS person for the Los Angeles, CA area. Client will hire off a phone screen and contract will run approximately 2 year. Rate anywhere between $50-52 per hour on the high end. Got anyone No in person interview required he will hire from phone interviews Must be onsite in Pasadena, CA (outside of LA area) Key Elements: - 5+ years overall SAS - Some MVS/TSO mainframe experience (does not have to be in current position but must know it) - Healthcare is highly desired, for example, it is helpful that the consultant understands what a Healthcare diagnosis code is…this is an example. Does not have to be direct healthcare can be research experience - Health claims data would be great - Will be taking existing programs and run them as they are already set up. Routine programming, tables, listings, etc. No development or macro development required. - Good communication skills *Regards* *Alex* -- You received this message because you are subscribed to the Google Groups Citrix and Sap problems group. To post to this group, send email to citrix-and-sap-probl...@googlegroups.com. To unsubscribe from this group, send email to citrix-and-sap-problems+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/citrix-and-sap-problems?hl=en.
Backfill - SAS clinical programmers.
*Send the profile to j...@tekatlantis.com * We have a opening, 18 months in duration, for strong SAS clinical programmers. Client: Non-profit organization Location: NY Rate: $38/hr best (job is secured for 1.5 years) JOB DESCRIPTION: Individuals in this position will work closely with the research teams to generate SAS programs for the analysis and the reporting of data from clinical trials for NDA submission, and for quality control and quality assurance processes. RESPONSIBILITIES: 1. Assist statistical, data management and project teams in the production of statistical reports. 2. Apply statistics/biostatistics knowledge to write and edit statistical programs to evaluate data; produce frequencies, cross tabs, t-tests, life tables and regressions. 3. Participate in edit check program development, testing and implementation as required by in house data management system. 4. Write SAS programs to assist data management team with quality control and quality assurance. 5. Interact with study team members to discuss programming data issues including synthesis of different data management systems i.e. DataFax and Smart Pen. 6. Participate in the ongoing preparation of SAS datasets for statistical analyses and presentations, e.g. listings, tables and graphics. 7. Participate in the preparation of the final databases for analysis. 8. Integrate and rationalize datasets when necessary. 9. Other data-related requests as assigned REQUIRED SKILLS: 1. B.A./B.S. in computer science, or related field, and a minimum of five years' SAS programming experience, particularly related to pharmaceutical clinical trials; M.S. in computer science statistics/biostatistics or related field desirable 2. Must have extensive knowledge of macro programming, the GRAPH and REPORT procedures. 3. Experience producing displays for FDA submission required. Knowledge, with prior production of displays, related to tabulation and statistical analysis preferred. 4. Experience in helping to design CRFs with statisticians, CRAs and data managers a plus 5. Experience with relational databases clinical trials required 6. Excellent analytical skills with exceptional attention to detail. 7. Experience with MedDRA and/or WHOART coding for adverse events of clinical trials preferred. 8. Ability to work independently as part of a team. 9. All candidates must have proof of authorization to work in the U.S. -- Alex Sr.Recruiter a...@tekatlantis.com Atlantis Technologies Inc. 5745 Weddington Dr, Cumming, GA 30040 www.tekatlantis.com -- You received this message because you are subscribed to the Google Groups Citrix and Sap problems group. To post to this group, send email to citrix-and-sap-probl...@googlegroups.com. To unsubscribe from this group, send email to citrix-and-sap-problems+unsubscr...@googlegroups.com. For more options, visit this group at http://groups.google.com/group/citrix-and-sap-problems?hl=en.
