Sr. Clinical Data Programming Scientist

Accenture in India

Mumbai

On-site

INR 1,800,000 - 2,800,000

Full time

14 days+

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Job summary

Accenture in India seeks a Sr. Clinical Data Programming Scientist to contribute to clinical data management within Life Sciences R&D. You will develop study databases, build electronic case report forms, and ensure data quality across trials while aligning with sponsor requirements.

You will collaborate with teams to implement data ingestion pipelines, automate workflows, and support regulatory submissions in a fast-paced environment.

Qualifications

  • Experience configuring, developing, and maintaining Elluminate-based data solutions.
  • Experience with clinical data management and trial data standardization.
  • Strong problem-solving skills and ability to work with cross-functional teams.

Responsibilities

  • Analyze moderately complex problems and develop solutions.
  • May create new solutions by adapting existing methods.
  • Interact with senior management, clients, and internal teams.
  • May manage small teams or work efforts on client projects.
  • This role may require rotational shifts.

Skills

Clinical data management
Elluminate Clinical Data Cloud
Data ingestion & transformation
Automation workflows
Reporting tools (JReview, Cognos, Spot

Education

BE
BTech

Tools

Elluminate
Spotfire
Qlik
JReview
Cognos
BOXI

Job description

Skill required: Clinical Data Services - Clinical Database Programming

Designation: Sr. Clinical Data Programming Scientist

Qualifications: BE,BTech

Years of Experience: 7 to 11 years

About Accenture

Accenture is a global professional services company with leading capabilities in digital, cloud and security. Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 784,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities. Visit us at www.accenture.com

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 clinical study databases by building electronic case report forms and program edit checks as per specifications. Support any updates or changes to the study database (e.g. Protocol amendments) through the change control process.

What are we looking for?
  • Adaptable and flexible
  • Ability to perform under pressure
  • Problem-solving skills
  • Ability to establish strong client relationship
  • Agility for quick learningStrong background in life sciences/clinical data management and proven expertise in configuring, developing, and maintaining solutions within the Elluminate Clinical Data Cloud environment. Hands-on experience in data ingestion, transformation pipelines, data standardization, automation workflows, and analytics enablement within Elluminate tool . Given the specialized nature of the platform, along with the niche skill set required to work across clinical data acquisition and integration workflows, an experienced resource is essential to ensure quality delivery, system optimization, and timely execution of sponsor requirements. Expertise in one or more reporting technologies (elluminate, Spotfire, Qlik, JReview, Cognos, BOXI, etc.) related to clinical drug development Roles and Responsibilities:
  • In this role you are required to do analysis and solving of moderately complex problems
  • May create new solutions, leveraging and, where needed, adapting existing methods and procedures
  • The person would require understanding of the strategic direction set by senior management as it relates to team goals
  • Primary upward interaction is with direct supervisor
  • May interact with peers and/or management levels at a client and/or within Accenture
  • Guidance would be provided when determining methods and procedures on new assignments
  • Decisions made by you will often impact the team in which they reside
  • Individual would manage small teams and/or work efforts (if in an individual contributor role) at a client or within Accenture
  • Please note that this role may require you to work in rotational shifts
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