Rave Programmer

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 utilise specialised software and systems to manage the data efficiently.

Develop and review complex edit checks, patient profile listings, reports, preprocessing checks and map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. Rave programming, Clinical Data, Medidata Rave, EDC, EDC Programming, study build, Inform CD.

Responsibilities:

• Ability to establish strong client relationships.
• Ability to handle disputes.
• Ability to manage multiple stakeholders.
• Ability to meet deadlines.
• Ability to perform under pressure.

Skills

Medidata Rave, Rave, clinical, database