| Pharma - IT Openings [message #106303] |
Wed, 19 February 2003 05:47  |
Vasu
Messages: 9
Registered: June 1999
|
Junior Member |
|
|
We do have an immediate requirement for our Bangalore based client which reads as mentioned below.
*SAS Clinical Trials:
-Location:(CA,CT,NJ)
5 yrs SAS programming experience preferably with good experience in SAS base and Macro Language.
Must have some clinical experience,understand the clinical development process,statistical analysis and reporting.
SAS clinical and AF experience along with SCL experience is desirable.
*Oracle Clinical Trials developer:
Location: (CA,CT)
-Manage the specification,documentation,validation and implementation of systems in support of clinical trials
-Analysis of clinical data requirements and recommendations and implementation
-Support clinical data activities
*Clinical Data Manager:
-Location:(CA)
-Planning,organisation and coordination of all internal and external data management activities supporting clinical trials
-Support the design,documentation,testing,implementation,validation and utilisation of systems and processes wihin
the Clinical Data Management area.
-Support the development and training of clinical data management
-Implements data management procedures compliant with regulatory requirements
-For assigned Clinica trials manage the assigned activities and resources as well as external contractual arrangemets.
*Clinical Data co-ordinator:
Location:(CA and NJ)
-Participates and coordinates the development,approval and maintenance of the data management plan for each clinical study
-Function as the data managements representative to clinical teams -Provides data management expertise to the team
-Coordinate data review and update process
-Interface with CRO's to ensure high quality and timely deliverables.
Good experience in datagate & eGate in a Healthcare environment
Interested candidates rush your resumes along with the position you are applying for to vasu_partha@yahoo.com
Regards
|
|
|
|
| Re: Pharma - IT Openings [message #106525 is a reply to message #106303] |
Sat, 31 January 2004 20:35  |
Bhaskar
Messages: 10
Registered: January 2002
|
Junior Member |
|
|
Hi,
At present i am working as a CDA(programmer) in an MNC company in India, Bangalore in Clinical data management centre. My skill sets includes SAS,oracle,Power builder, VB. Please let me know if you have any openings in pharma sector for my profile.
regards,
baskar
|
|
|
|
| Re: Pharma - IT Openings [message #121509 is a reply to message #106525] |
Mon, 30 May 2005 07:01 |
wraj3
Messages: 26
Registered: April 2005
Location: Mumbai-India
|
Junior Member |
|
|
Hi BHaskar,
We are looking for Sr CDM Programmer with TCS and I am passting below a detailed job specs with this mail
Position: Senior Clinical Database Programmer for Clinical Data Management (CDM) unit
Location: Mumbai
Responsibilities:
Ø To manage the day-to-day activities within the Programming group in CDM.
Ø To co-ordinate and manage programming activities within the Clinical Trials Space for a customer/group of projects.
Ø Ensures the adherence to industry standards and regulatory requirements, including but not exclusive to Good Clinical Practices (GCP), Validate CDM systems, CDSIC etc.
Ø Create relevant SOPs.
Ø To ensure development of personal skills of the personnel in programming group.
Ø Provide training in the CDM / Programming Space
Ø Interacts and lieu with the Life Science and Healthcare Practice group in-house.
Requirements
Ø 4+ Years programming experience in CDM space in clinical trials with minimum degree in science - Mathematics/Statistics.
Ø Well Conversant with Oracle Clinical 3.2 (4.0.3 preferred), working experience in systems like SAS, Clintrial, Inform, other CDM systems will be an added advantage.
Ø Creating/updating Clinical Data management documents relevant to programming.
Ø Ensure that projects are completed within budget constraints.
Ø Creating/Assists in maintaining and updating the relevant statistical SOPs.
Ø Ability to play a leadership role within the programming group including project management (resources, timelines).
Ø Understanding of regulatory requirements and best practices related to clinical data management activities.
Ø Provide appropriate input to the design of Case Report Forms.
Ø Conversant with overall Information Technology applications in Clinical Data Management.
Ø Identify & provide relevant training to the programming group in the CDM space
Kindly revert with ur interest and match with an updated resume and ur current contact details
Also let me know ur current cost to company and ur interest in relocating to India
Regards
Rajendra
wraj3@rediffmail.com
91 22 6601301, 02
|
|
|
|
] 
Blog
Search
Help
Members
Register
Login
Home
