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Clinical Programmer Remote Job at Atorus Research Apply Now

Apply for Clinical Programmer Job at Atorus Research 2026. Check eligibility, salary, remote work details, and online application process today.

Introduction

The demand for skilled professionals in clinical data programming continues to rise as clinical trials become more technology-driven. If you are experienced in EDC systems and looking for a flexible work environment, this opportunity could be ideal. The Clinical Programmer Job at Atorus Research offers remote work, global exposure, and a strong career path in clinical research technology.

Professionals with expertise in platforms like Veeva CDMS and Medidata Rave can leverage this role to work on advanced clinical trials and data-driven projects.


Job Overview

Job DetailsInformation
Job TitleClinical Programmer
Company NameAtorus Research
LocationRemote (Hiring Base: Bengaluru)
Employment TypeFull-Time
DepartmentClinical Data Management / EDC Programming
Experience Required1–5 Years
EducationBachelor’s Degree (Life Sciences, Pharmacy, or related field preferred)
Salary₹6 LPA – ₹12 LPA (Estimated)

Company Overview

Atorus Research is a globally recognized organization specializing in clinical data analytics, programming, and biometrics solutions. The company focuses on improving clinical trial efficiency through automation and innovative data technologies.

Working here provides professionals with exposure to international clinical studies, modern EDC tools, and a collaborative work culture that promotes continuous learning.


Job Location & Employment Type

  • Work Mode: 100% Remote
  • Base Location: Bengaluru, India
  • Employment Type: Full-Time

This remote setup makes it an excellent opportunity for professionals across India seeking flexibility without compromising on career growth.


Open Positions / Department Details

  • Role: Clinical Programmer (EDC Programmer)
  • Department: Clinical Data Management

The role primarily involves building and managing clinical trial databases while ensuring data quality and regulatory compliance.

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Key Roles & Responsibilities

  • Design and develop clinical databases using EDC platforms
  • Create and configure eCRFs based on study requirements
  • Perform custom function programming and edit check implementation
  • Handle study build activities, including deployment and updates
  • Work extensively with Veeva CDMS or Medidata Rave systems
  • Ensure adherence to ICH-GCP guidelines and company SOPs
  • Provide technical support for data collection systems
  • Collaborate with internal teams and external stakeholders
  • Manage multiple projects and meet strict timelines efficiently

Eligibility Criteria

Education

  • Bachelor’s degree in Life Sciences, Pharmacy, or related discipline

Experience

  • 1 to 5 years of hands-on experience in EDC programming

Skills Required

  • Strong knowledge of Veeva CDMS or Medidata Rave
  • Experience in custom function programming
  • Expertise in eCRF development and edit checks
  • Understanding of study configuration (events, forms, schedules)
  • Familiarity with object hierarchy in Veeva CDMS
  • Good communication and client interaction skills
  • Ability to manage multiple deliverables

Preferred Qualification:

  • Veeva Study Builder Certification

Salary & Benefits

  • Estimated Salary: ₹6 LPA – ₹12 LPA (depending on experience)
  • 100% remote working flexibility
  • Opportunity to work on global clinical trials
  • Exposure to advanced analytics and clinical technologies
  • Learning-focused environment with career growth opportunities

Selection Process

The recruitment process typically includes:

  1. Application screening
  2. Technical assessment or interview
  3. HR discussion
  4. Final selection

How to Apply

Interested candidates can apply through the online application method provided by the company. Ensure your resume highlights relevant EDC programming experience and technical skills.


Important Dates

  • Application deadlines are not specified, so early application is recommended

Why Apply for This Job?

Choosing the Clinical Programmer Job at Atorus Research can significantly boost your career in clinical data management. Here’s why this role stands out:

  • Work remotely while collaborating on global projects
  • Gain hands-on experience with leading EDC platforms
  • Improve your technical and analytical skills
  • Be part of a forward-thinking, data-driven organization
  • Access continuous learning and career advancement opportunities
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This role is especially valuable for professionals aiming to transition into advanced clinical programming and data analytics domains.


FAQs

1. What is the eligibility for Clinical Programmer Job at Atorus Research?

Candidates must have a bachelor’s degree in Life Sciences, Pharmacy, or a related field with 1–5 years of EDC programming experience.

2. What is the salary for this role?

The estimated salary ranges between ₹6 LPA and ₹12 LPA based on experience and skills.

3. Is this a remote job?

Yes, this is a fully remote position with a Bengaluru hiring base.

4. Which tools are required for this role?

Candidates should have experience in Veeva CDMS or Medidata Rave along with eCRF and custom function programming.

5. How can I apply?

You can apply through the official online application link provided by the company.


Conclusion

The Clinical Programmer Job at Atorus Research 2026 is an excellent opportunity for professionals looking to grow in clinical data programming and EDC systems. With remote flexibility, competitive salary, and exposure to global clinical trials, this role offers both stability and career advancement.

If you meet the eligibility criteria, applying early can increase your chances of selection.


Disclaimer

IndiaPharmaJobs.in is an independent job information platform. We do not provide jobs or recruitment and are not affiliated with any company.


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