*send me your updated profile at dhee...@zodiac-solutions.com
<dhee...@zodiac-solutions.com>*


Hi,



I have an urgent requirement with one of my clients, details given below.
If you find yourself suitable for the position, please send me your latest
updated resume along with contact details. Please include your employer
details as well.



*Job Title:                                 * *Clinical Developer*

*Location**:                                   Monmouth Junction, NJ  *

*Job Type:                                  **Contract*

*Duration:                                   **6+  Months*

*Interview:                                  **Telephonic + Skype*






*POSITION SUMMARY *Designs, develops and maintains clinical data
transformations conformant to biopharmaceutical industry data model
standards and provide expertise to clinical teams developing data capture /
data management solutions to maintain compliance with these standards.

*PERSONAL QUALITIES*
Ability to function in a highly collaborative fast paced team environment.
Excellent analytical skills with the ability to manage multiple priorities
and requests. Excellent communication and interpersonal skills.

*SKILLS NEEDED*

. Ability to review and interpret clinical trial documentation
. Excellent problem resolution follow-up skills to ensure all projects are
handled in a timely manner.
. Ability to work independently in a fast paced environment.
. Strong work ethic and willingness to learn.
. Proficiency with Microsoft Office tools
. Excellent communication, presentation and documentation skills

*QUALIFICATIONS NEEDED*
. BS or MS degree in Computer Science, Statistics, Life Sciences or other
relevant scientific subject with 3+ yrs or BS degree with 5+ yrs of
relevant experience
. Understanding of clinical compliance requirements.
. Understanding of GCP/ICH guidelines for conduction of clinical trials.
. Thorough understanding of SQL programming.(T-SQL/SSRS/SSIS)
. Direct experience in support of clinical trials with emphasis on
development of SDTM datasets and programming of Tables Listings and Figures
. Knowledge of Clinical Trial lifecycle
. Understanding 21-CFR Part 11 guidelines
. Working knowledge of at least one Electronic Data Capture System
. Intermediate knowledge of XML and C#(Will train if needed)

*PLUS:*
Experience with SAS programming





* “**The best preparation for tomorrow is doing your best today**”*



*Thanks & Regards,*

*Dheeraj Chauhan*

*Technical Resource Specialist*

*880 E Swedesford Road, Suite #210|Wayne, PA 19087*

*Phone :  484-436-4300*

Email : *dhee...@zodiac-solutions.com* <dhee...@zodiac-solutions.com>

URL : www.zodiac-solutions.com

*G talk/hangout : **dheeraj.rgtal...@gmail.com <dheeraj.rgtal...@gmail.com>*

-- 
You received this message because you are subscribed to the Google Groups 
"International SAP Projects" group.
To unsubscribe from this group and stop receiving emails from it, send an email 
to international-sap-projects+unsubscr...@googlegroups.com.
To post to this group, send email to 
international-sap-projects@googlegroups.com.
Visit this group at https://groups.google.com/group/international-sap-projects.
For more options, visit https://groups.google.com/d/optout.

Reply via email to