Job Title:       SpotFire Developer
Location:       Philadelphia , US

Duration:       6+ Months

Skills : Strong hand at SpotFire with clinical domain knowledge



*JOB RESPONSIBILITIES*:



Ø  The ideal candidate will have a background in clinical programming in a
data management setting or statistical setting.

Ø  Raising the request to setup the study id in spotfire file share area.

Ø  Adding the workflows using the Study Configuration tool.

Ø  Creating the Data visualization using the codes placed in spotfire file
share area.

Ø  Embedding the study dataset into the workflow.

Ø  Open the workflow using Spotfire (via citrix). Modify the data
visualization as per check requirement.

Ø  Creating the Study Specific Data visualization based on specification.

Ø  The ability to focus on customer needs, troubleshooting, and providing
innovative technical solutions, while adhering to standards is essential.

Ø  This is a dynamic position that will require the successful candidate to
learn a number of bespoke systems and solutions and implement those
effectively in order to deliver a top-notch conversion service.



ü  Project management

ü  Communication

ü  Data management understanding

ü  Good SAS programming skills





*Additional Activities:*



·          Support multiple functional groups (i.e. DM, S&P, etc) across
all phases

·          Lead and actively participate in review of Spotfire deliverables

·          Create & Maintain process documentation as required

·          Lead or participate in process redesign & optimization

·          SAS programming for creation / review of Spotfire domains as
required

·          Training of new staff on the role

·          Provide training/guidance on Spotfire process for teams

·          Provide oversight to offshore team



*Additional preferred skills:*



·         Experience extracting and transforming clinical data

·         Knowledge of clinical trial processes and supporting systems

·         Strong skills in SQL, PL/SQL.

·         Knowledge of FDA requirements for annotated CRFs

·         Experience with eDC/eDM setup for clinical trials





*QUALIFICATIONS & SKILLS:*



Ø  Bachelors’ degree in a scientific / technical discipline.

Ø  Programming Knowledge:SQL, PL/SQL, COGNOS, C#

Ø  Effective communication skills. (Verbal and Written).

Ø  4+ years of experience in SAS and SpotFire programming (Pharmaceutical
Industry) and familiarity with CDMS is desirable.

Ø  Ability to work across different platforms like VB, UNIX, and remote
data capture technology is preferred.







*BEHAVOIURS/ COMPETENCIES*:



Ø  Ability to speak to non-technical audience with assertiveness.

Ø  Knowledge of Quality control and Quality assurance.

Ø  Time management skills.

Ø  Collaboration and team work

Ø  Knowledge of regulatory requirements for electronic submission.

Ø  Assertiveness in explaining issues and ability to make recommendations.





*Thanks & Regards*



*Hemendra Kumar*

Insigma Inc | 1920 Association Drive Suite # 302, Reston, VA 20191

Phone: 703-468-3024  I Email: hemendra.ku...@insigmainc.com



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