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Dear Allstat, Please find below our 2 latest perm opportunities:- Expert CDM Programmer Permanent Global Pharma Based in Netherlands(100% Client site) Competitive salary KEY RESPONSIBILITIES: * Provide expert technical guidance and programming support (e.g., SAS, SQL, relational databases, etc.) for CDM utilities * Lead the design, development, validation, implementation, and maintenance of complex programs, or suites of programs, in support of monitoring, reporting, and analysis of clinical trial data * Lead interactions with global users and clients to collect and refine requirements, and make compelling proposals for new or updated utilities or processes * Act as Software Manager for CDM programs, including maintenance of CDM program inventory and validation documentation * Troubleshoot complex problems on CDM programs, in particular where expert technical skills are required * Provide training to programmers and users of all levels * Provide programming support for complex ad-hoc questions * Support maintenance of global clinical trial database standards (CDISC) in the SAS CDR * Support SAS interfaces to EDC, Clintrial, Clintrack, Coding system, Serology lab, with expert technical guidance, programming and validation for maintenance activities and upgrades. * Interact with the SAS vendor that is hosting the SAS CDR on technical issues * Lead upgrades of SAS from a CDM program perspective, including validation documentation development, review and execution Minimum requirements: * Minimum 4 years industry experience * Excellent SAS programmer * Can offer a variety of solutions to design an new utility or resolve a technical issue * Expert knowledge of SAS and SQL * Expert knowledge of CDISC standards (CDASH and SDTM) * Clinical systems and account administration and security * Ability to set and meet timelines Principal Biostatistician Permanent Global Pharma Based in Netherlands (100% Client site) Competitive salary KEY RESPONSIBILITIES: * Provide adequate and qualified statistical and methodological support in order to ensure the appropriate methodological and statistical approach * Contribute to the design of studies in order to ensure studies are set up to meet their (primary) objectives. * Together with the study clinician clarify and communicate the results and conclusions to the organization in order to ensure the correct interpretation of the results by different users. * Contributes to the preparation of submission dossiers and in the response to regulatory agencies in case of questions * Fully exploits the potential of the clinical (integrated) data in-house available in our data warehouse as well as utilizes external data in order to enhance the knowledge of the compound. * Review statistical literature and attends conferences and courses in order to ensure a high statistical expertise and maintain proficiency. Minimum requirements: * PhD or MSc in Biostatistics/Statistics/ Mathematics * Minimum 8 years of related industry experience * Experienced in working with external partners * Challenges current practices to improve quality * Seizes opportunities and develops ideas * Has strategic orientation and promotes expertise * Able to manage different concurrent projects For a confidential consultation call Laura Christie on +44 203 465 0083 or email your CV to [log in to unmask]<blocked::mailto:[log in to unmask]> I look forward to hearing from you. Kind regards, Laura Laura Christie Team Leader, Biometrics & HEOR, Europe Recruiting experts in Life Sciences HAYS Recruiting experts worldwide 107 Cheapside London EC2V 6DB T: +44 203 4650 068 M: +44 7900 932031 F: +44 203 465 0001 E: [log in to unmask]<mailto:[log in to unmask]> Please add me on Linked In<http://uk.linkedin.com/pub/laura-christie/18/492/6b9> Refer a friend to Hays<http://www.hays.co.uk/refer-a-friend/> and receive vouchers as a reward when we place them in a new role. hays.co.uk<http://www.hays.co.uk/> ------------------------------------------------ ********************************************************************* Disclaimer This message (including any attachments) is confidential and may be legally privileged. If you are not the intended recipient, you should not disclose, copy or use any part of it. 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