Hi,
We are working on below requirement . Please submit resumes of your resources with rate and contact details to proceed further.
Location:
Duration: 6+ Months
Rate: $50/Hr
Local to New jersey preferred.
Skill set:
- Provide statistical programming support and validation and help set specifications of analysis datasets, pooled datasets, statistical tables, summaries, figures and listing for Phase II-IV clinical trials.
- Strong Pharma experience in recent projects
- Employ standardized programs where applicable.
- Provide input into planning documents such as protocol, validation plan, and report analysis plan.
- Provide outputs for clinical study reports, integrated summaries and electronic submissions.
- Help respond to health authority inquiries for submitted dossiers.
- Establish and maintain sound working relationship and effective communications within biostatistics and statistical reporting and clinical research.
- 2-3 years of Analytical experience.
- BA/BS or equivalent experience in computer science, mathematics, statistics, life sciences, or related field(s).
- Good SAS programming skills, with 4 years experience in a pharma setting, preferably working with clinical trial data.
- Good understanding of clinical trial practices, procedures and methodologies.
- Good verbal and written communication skills.
- Good interpersonal and organizational skills.
- Attention to detail and correctness.
- Working knowledge of office tools
Please call/ Email for further details...
Thanks and Regards,
Naren,
Resource Manager
Contact:847-621-7346,847-798-4287
Kalven Technologies, Inc
http://www.kalventech.com
"Providing Quality Technology Solutions"
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