Clinical Data Svs Specialist

7 - 12 years

Bengaluru

Posted:8 months ago

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Job Description



Skill required:
Clinical Data Services - Clinical Database Programming

Designation:
Clinical Data Svs Specialist

Qualifications:
BE

Years of Experience:
7 to 11 years

What would you do?
You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world¢??¢s leading biopharma companies bring their vision to life ¢??? enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Clinical Data Services involve the management and processing of data collected during clinical trials. This includes data collection, validation, storage, and analysis to ensure the data is accurate and reliable. The goal is to support clinical research by providing high-quality data that can be used to evaluate the safety and efficacy of medical treatments. These services are essential for regulatory compliance and successful trial outcomes. They often utilize specialized software and systems to manage the data efficiently.Develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems.

What are we looking for?
?¢Adaptable and flexible?¢Ability to perform under pressure?¢Problem-solving skills?¢Detail orientation?¢Ability to establish strong client relationship

Roles and Responsibilities:
Overall experience of 4+ years with exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva etc. preferred. o Extensive experience in database design, edit check programming, custom function programming and unit testing. o Experienced in various modules such as IVRS/RWS integration and Lab administration.?¢Medidata RAVE study builder certified preferred.
 Qualification BE

Skills Required

clinical data data services oracle regulatory compliance cognos pharmacovigilance data collection database design r database programming clinical research compliance client relationship clinical trials life sciences programming

Work Mode

Work from Office

Job Type

Full Time

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