Dear Allstat,
Please find below our latest contract:-
CDM Programmer III
6 month rolling contract
Global Pharma
Based in Netherlands(100% Client site)
Competitive hourly rate
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, as well as other requests from within or outside of the department.
- 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
- Provide direct global user support on CDM programs
- 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 CDR 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 CDR from a CDM program perspective, including validation documentation development, review and execution.
- Maintain strong working relations with colleagues in global biometric departments
- Provide professional programming input for new program or program enhancement requests
- Author and review SOPs and work instructions
- Adhere to the relevant departmental SOPs, corporate policies, regulatory requirements and industry best practices
- Act as project and/or technical lead for innovative projects, such as implementation of new systems and/or processes
- May be assigned as Backup for senior Clinical Systems Administrator
Minimum requirements
- Excellent SAS programmer
-Typically, 5 or more years of relevant working experience in SAS programming, preferably in the biotechnology or pharmaceutical industry
- Can offer a variety of solutions to design an new utility or resolve a technical issue
- Good computer skills
- Expert knowledge of SAS and SQL
- Expert knowledge of CDISC standards (CDASH and SDTM)
- Clinical systems and account administration and security
- Understands clinical data
- Good interpersonal and communication skills
- Problem solving skills
- Accurate worker with attention to relevant details
- Ability to set and meet timelines
- Good project management skills
For a confidential consultation call Laura Christie on +44 207 633 4825 or email your CV to [log in to unmask]
I look forward to hearing from you.
Kind regards,
Laura
Laura Christie
Principal Consultant, Biometrics, Europe
Recruiting experts in Pharma
HAYS Recruiting experts worldwide
25-27 Wootton Street
London
SE1 8TG
T: +44 207 633 4825
M: +44 7900 932031
F: +44 207 922 7101
E: [log in to unmask]<mailto:[log in to unmask]>
hayspharma.com
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