*Hi *

*Please find below details for the position of SAS Programmer  send me your
updated resume.*

*Position:                              SAS Programmer Analyst*

*Location:                             Cambridge, MA*

*Duration                              6+ month               *

*Interview:                            Phone Interview/Hire*

* Summary: The position is responsible for leading clinical programming
activities in one or more regions or therapeutic areas. Ensure adequate
oversight to outsourced activities by performing quality control steps.
Essential Duties and Responsibilities: 1) Lead or contribute to the design,
creation and lifecycle management of data collection, validation, analysis
and/or reporting systems/software programs (e.g. SAS). For outsourced
studies provide oversight to these activities. 2) Lead clinical data
standards development and governance activities (e.g. Implementation of
CDISC data models like SDTMs, ADaMs, define.xml, LAB, ODM, etc.) and
apply/oversee the application of the CDISC data models during the clinical
and statistical programming activities. 3) Review relevant DMP sections,
CRF design/specifications, SAP and Mock-up tables to provide input from
CDISC/Programming perspectives. 4) Develop specifications for multiple data
transfers and manage/oversee the actual Data Transfers. 5) _Check the
content and format of CDISC submission packages for completeness and
compliance with internal and regulatory standards. 6) Assist in the
development of resourcing plans and support the training and development of
colleagues (e.g. junior Programmers). 7) Manage partnerships with CROs in
order to support business goals and proactively address operational issues
related to clinical systems or programming.. *

* Qualifications:*

* • SAS programming expertise • Excellent analytical, problem-solving,
organizational, time-management, interpersonal and communication skills •
Ability to work on multidisciplinary team and to prioritize activities. •
Knowledge of all aspects of the clinical trials process from pre-clinical
to post-marketing phases • Ability to interpret and apply regulatory
requirements • Knowledgeable concerning all aspects of qualification and
compliance assessments • Demonstrated ability to effectively manage
relationships with CROs • Experience/Exposure to exercising quality
oversight. • Technical understanding of clinical research technologies and
software development methodologies • Experience in systems integration and
the application of data interchange standards (e.g. CDISC) • Proficient in
the use of one or more of the leading Clinical Database Management Systems
and clinical/statistical programming environments • Experience supporting
continuous process improvement initiatives with a proven track record of
success as measured by return on investment • Current with industry
developments and trends Education and/or Experience: 2+ years / 4+ years of
clinical systems or programming experience in the Pharmaceutical, Device or
Biotech industries (Sponsor, CRO or combination) in roles of increasing
responsibility. Bachelor’s degree required. Master's degree preferred*

Thanks and have a great day

*Ranjeet Kumar*

*Technical Recruiter*

*Srimatrix Inc.*

*Phone No. 469.320.9415*

*Email: rku...@srimatrix.com <rku...@srimatrix.com>*

You received this message because you are subscribed to the Google Groups "Open 
Source Erp & Crm" group.
To unsubscribe from this group and stop receiving emails from it, send an email 
to open-source-erp-crm+unsubscr...@googlegroups.com.
To post to this group, send email to open-source-erp-crm@googlegroups.com.
Visit this group at https://groups.google.com/group/open-source-erp-crm.
For more options, visit https://groups.google.com/d/optout.

Reply via email to