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Introduction
If you are looking to build a strong career in clinical data management and study design, this opportunity can be a perfect fit. The Clinical Study Builder at Indero role offers a chance to work on advanced clinical data systems and contribute to global research projects. With growing demand for skilled professionals in CDMS platforms, this role is ideal for candidates aiming for long-term growth in clinical research.
Job Overview
| Field | Details |
|---|---|
| Job Title | Clinical Study Builder |
| Company Name | Indero |
| Location | India (Work from Home) |
| Employment Type | Full-Time, Permanent |
| Department | Biometrics / Clinical Data Management |
| Experience Required | Minimum 2 Years |
| Education | B.Sc., M.Sc. or related field |
| Salary | As per company norms |
Company Overview
Indero is a globally recognized Clinical Research Organization (CRO) specializing in dermatology and rheumatology studies. With more than two decades of industry experience, the company has built a strong reputation for delivering high-quality clinical trials across multiple regions including North America, Europe, Asia-Pacific, and Latin America.
Indero focuses on end-to-end clinical solutions—from study design to data analysis—making it a trusted partner for pharmaceutical and biotech companies worldwide.
Job Location & Employment Type
This is a home-based (remote) opportunity in India, allowing professionals to work flexibly. However, candidates must be comfortable attending occasional meetings outside regular working hours due to global collaboration.
Employment type is full-time and permanent, offering long-term career stability.
Open Positions / Department Details
The role is part of the Biometrics and Clinical Data Management team, which plays a critical role in ensuring accurate and efficient handling of clinical trial data.
Professionals in this department are responsible for designing, building, and managing electronic data capture systems used in clinical studies.
Key Roles & Responsibilities
- Develop and configure electronic Case Report Forms (eCRFs) using Veeva CDMS and other EDC systems
- Create folders, edit checks, derivations, integrations, and reports based on study protocols
- Design visit schedules aligned with clinical study requirements
- Configure modules such as Coder, Local Lab, and Targeted SDV
- Lead eCRF design discussions and review meetings with stakeholders
- Provide technical support and guidance to users and study teams
- Conduct training sessions for end-users on CDMS platforms
- Collaborate closely with Lead Data Managers and cross-functional teams
- Work with external vendors during system testing and deployment
- Identify and resolve system issues efficiently
- Contribute to SOP development and updates for Veeva CDMS
- Ensure compliance with regulatory standards such as GCP and ICH guidelines
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in Life Sciences, Clinical Research, or related discipline
Experience
- Minimum 2 years of hands-on experience in Veeva CDMS study build
- Experience with platforms like Medidata Rave or Medrio is preferred
Skills Required
- Strong understanding of clinical trial processes and data management
- Knowledge of GCP (Good Clinical Practice) and ICH guidelines
- Experience in eCRF design and database programming
- Ability to manage multiple projects simultaneously
- Excellent communication skills in English
- Strong problem-solving and analytical skills
- Time management and organizational abilities
Salary & Benefits
- Salary: As per company norms
- Flexible work schedule
- Permanent full-time employment
- Continuous learning and development programs
- Exposure to global clinical research projects
- Opportunity to work with experienced professionals
Selection Process
The hiring process typically includes:
- Application screening
- Technical interview (CDMS and study build knowledge)
- HR interview
- Final selection and offer
How to Apply
Interested candidates can apply through the online application method provided by the company’s official career portal. Ensure your resume highlights relevant CDMS and clinical data management experience.
Important Dates
- Application Deadline: Not specified (Apply as early as possible)
Why Apply for This Job?
This role is highly valuable for professionals aiming to grow in clinical data management and clinical research technology. Here’s why you should consider applying:
- Work remotely while collaborating on global clinical trials
- Gain expertise in industry-leading platforms like Veeva CDMS
- Enhance your technical and project management skills
- Be part of a reputed CRO with strong global presence
- Access continuous learning and career advancement opportunities
FAQs
1. What is the main focus keyword for this job?
The focus keyword is Clinical Study Builder Indero.
2. Can freshers apply for this role?
No, this position requires at least 2 years of relevant experience.
3. Is this a remote job?
Yes, it is a work-from-home opportunity within India.
4. What skills are important for this role?
Key skills include Veeva CDMS experience, eCRF design, data management, and knowledge of GCP guidelines.
5. What is the salary offered?
Salary is not disclosed and will be provided as per company standards.
Conclusion
The Clinical Study Builder at Indero position is an excellent opportunity for experienced professionals in clinical data management. With remote flexibility, global exposure, and strong career growth potential, this role is ideal for those looking to advance in the pharmaceutical and clinical research industry. Apply soon to secure your chance in this competitive field.
Disclaimer
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