MS Clinical Research Hiring Data Monitoring & eCRF Designer in Bengaluru | Clinical Data Management Jobs 2026
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(MS Clinical Research Hiring Data Monitoring & eCRF Designer in Bengaluru) |
Introduction
Candidates searching for clinical data management jobs in India now have an excellent opportunity to work with MS Clinical Research as a Data Monitoring & eCRF Designer in Bengaluru. The company is looking for professionals who are interested in clinical research operations, electronic Case Report Form (eCRF) design, data monitoring, and regulatory compliance activities.
This opportunity is especially valuable for candidates from B.Pharm, M.Pharm, Life Sciences, Biotechnology, and Clinical Research backgrounds who want to build a long-term career in clinical trial data systems and healthcare analytics. The role provides exposure to real-world clinical studies, data validation processes, query management, and clinical database workflows.
With the pharmaceutical and clinical research industry rapidly growing in India during 2026, skilled professionals in Clinical Data Management (CDM) and eCRF systems are becoming highly demanded across CROs and healthcare organizations.
About The Company
MS Clinical Research is a clinical research and healthcare solutions organization involved in clinical trial support, research data handling, regulatory documentation, and healthcare technology solutions. The company focuses on maintaining quality clinical data systems while supporting clinical research projects aligned with global regulatory standards.
The organization works in areas such as clinical trial management, electronic data capture systems, regulatory support, and healthcare research operations. MS Clinical Research aims to improve clinical research efficiency through technology-driven solutions and structured data management practices.
Company Details
- Company Name: MS Clinical Research
- Industry: Clinical Research & Clinical Data Management
- Headquarters: Bengaluru, Karnataka, India
- Founded: Information not officially disclosed publicly
- Employee Strength: Growing clinical research workforce in India
- Work Model: Full-time On-site
The company provides opportunities for candidates looking to gain practical exposure in clinical data review, monitoring activities, and clinical database management systems.
Job Overview Summary
MS Clinical Research is hiring for the position of Data Monitoring & eCRF Designer at its Bengaluru office. This position combines responsibilities related to clinical data management, eCRF development, data validation, and study monitoring.
Selected candidates will work closely with clinical research teams to ensure the quality, consistency, and accuracy of clinical trial data collected during studies. The role also includes supporting database testing, query management, and maintaining regulatory compliance standards.
This is a strong opportunity for candidates aiming to build careers in Clinical Data Management (CDM), Pharmacovigilance (PV), Clinical Trials, and Electronic Data Capture (EDC) systems.
Vacancy Details
| Job Details | Information |
|---|
| Company Name | MS Clinical Research |
| Job Role | Data Monitoring & eCRF Designer |
| Job Location | Bengaluru, Karnataka, India |
| Job Type | Full-time |
| Industry | Clinical Research / Clinical Data Management |
| Experience Required | 1 – 5 Years |
| Qualification | B.Pharm, M.Pharm, Life Sciences, Biotechnology, Clinical Research |
| Work Mode | On-site |
| Department | Clinical Data Management |
Responsibility Explanation
1. eCRF Design & Development
Candidates will be responsible for designing and developing electronic Case Report Forms (eCRFs) using Zoho Database systems according to study protocols and clinical trial requirements. The role requires a proper understanding of data collection standards used in clinical studies.
2. Clinical Data Monitoring
The selected professional will monitor study data to ensure accuracy, consistency, and completeness. Data review activities help maintain reliable clinical trial records for further analysis and regulatory submission.
3. Data Validation & Query Resolution
One of the important responsibilities includes identifying discrepancies in clinical datasets, generating queries, and coordinating with investigators or study teams for correction and clarification.
4. User Acceptance Testing (UAT)
Candidates may assist in testing clinical database functionality before implementation. This process ensures that eCRF systems work correctly and support smooth study execution.
5. Regulatory Compliance Support
The role requires maintaining compliance with ICH-GCP guidelines and standard clinical research regulations. Proper documentation and audit-ready records are important parts of the job profile.
6. Collaboration with Clinical Teams
Employees will coordinate with clinical operations teams, investigators, and stakeholders involved in multiple studies to ensure smooth project execution and timely database lock activities.
Eligibility Criteria
Educational Qualification
Candidates with the following qualifications can apply:
- B.Pharm
- M.Pharm
- Life Sciences
- Biotechnology
- Clinical Research
- Relevant Healthcare or Science Degree
Experience Required
- 1 to 5 years of relevant experience in Clinical Data Management or Clinical Research.
Basic Knowledge Required
- Clinical Data Management (CDM)
- eCRF design and validation
- Clinical trial workflows
- ICH-GCP guidelines
Skills Required
Candidates applying for this clinical research job should possess several important technical and professional skills.
Technical Skills
- Knowledge of Electronic Data Capture (EDC) systems
- Understanding of eCRF design principles
- Data cleaning and query management knowledge
- Familiarity with clinical trial databases
- Knowledge of clinical study documentation
Soft Skills
- Strong analytical thinking
- Good communication abilities
- Attention to detail
- Team collaboration skills
- Problem-solving capability
- Ability to manage multiple studies simultaneously
Preferred Skills
- Experience with Zoho Database
- Exposure to clinical trial processes
- Understanding of regulatory documentation workflows
Salary Estimate
The estimated salary for this role may range between ₹3 LPA to ₹6 LPA, depending on candidate experience, technical skills, and previous exposure to Clinical Data Management systems.
Professionals with hands-on experience in EDC platforms, eCRF development, and clinical database workflows may receive better compensation packages in the clinical research industry.
Additional career benefits may include:
- Exposure to real-world clinical trial projects
- Career growth in Clinical Data Management
- Experience with regulatory-compliant systems
- Opportunity to move into the Pharmacovigilance and Clinical Operations domains
Interview Details
Selection Process
The recruitment process may include:
- Resume Shortlisting
- HR Discussion
- Technical Interview
- Final Selection Round
Interview Topics
- Clinical Data Management basics
- eCRF concepts
- Clinical trial process understanding
- Query management
- ICH-GCP guidelines
- Communication and analytical skills
Apply Method
Candidates can apply through the official LinkedIn application link provided below:
Application Link:
Required Documents
Candidates should keep the following documents ready before applying:
- Updated Resume/CV
- Educational Certificates
- Experience Certificates (if applicable)
- Government ID Proof
- Passport-size Photograph
- Skill Certifications (if available)
- Internship or Training Documents
- Clinical Research Certifications (optional)
Frequently Asked Questions (FAQs)
1. What is the job role offered by MS Clinical Research?
The company is hiring for the position of Data Monitoring & eCRF Designer in Bengaluru.
2. Who can apply for this clinical research job?
Candidates with B.Pharm, M.Pharm, Life Sciences, Biotechnology, or Clinical Research backgrounds can apply.
3. Is experience mandatory for this role?
Yes, candidates with 1–5 years of experience are preferred.
4. What skills are important for this job?
Knowledge of Clinical Data Management, eCRF design, query management, and ICH-GCP guidelines is important.
5. What is the expected salary for this role?
The estimated salary range is around ₹3 LPA to ₹6 LPA.
6. Is this a work-from-home job?
No, this is a full-time on-site role based in Bengaluru, Karnataka.
7. Which database platform is mentioned in the job role?
The role involves working with the Zoho Database for eCRF development activities.
8. Can freshers apply for this position?
The company prefers candidates with some experience, but candidates with strong clinical research knowledge may also explore the opportunity.
Final Conclusion
MS Clinical Research’s Data Monitoring & eCRF Designer opening in Bengaluru is a valuable opportunity for candidates interested in Clinical Data Management, eCRF systems, and clinical research operations. The role offers practical exposure to clinical trial data workflows, database management, and regulatory-compliant healthcare systems.
As the demand for skilled professionals in Clinical Research, Pharmacovigilance, and Clinical Data Management continues to increase in India during 2026, candidates with strong technical knowledge and analytical abilities can build stable, long-term careers in this sector.
Interested applicants should apply early and prepare a professional resume highlighting their clinical research skills, database knowledge, and understanding of clinical trial processes.
Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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