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Senior Data Standards Expert
Bangalore, Karnataka, India
Actively hiring, first seen by us 3 days ago- Pay
- Pay not listed
- Work setting
- Not stated
- Employment
Full-time — employment source
Employment type in the employer’s posting: Full-time
From the employer’s posting
What you’ll work on
Full postingDesign high-quality electronic case report forms for global clinical studies
Lead complex study builds in electronic data capture systems
Manage metadata and standards libraries
Oversee standards deliverables from external partners
Mentor colleagues and drive standards governance improvements
From the employer’s posting
design high-quality electronic case report forms for global clinical studies
You will lead complex study builds in electronic data capture systems
manage metadata and standards libraries
You will oversee standards deliverables from external partners
you will mentor colleagues and drive improvements in standards governance, automation and emerging data formats
What you’ll bring
All qualificationsCore experience
- 6-8 years in clinical data standards, data management or eDC design
- Advanced degree in life sciences, computer science or equivalent experience
- Strong CDISC, CDASH, SDTM, metadata and CRF design expertise
- Experience leading complex studies and cross-functional projects
- Knowledge of regulatory submissions and validation tools
Qualification wording
6 - 8 years in clinical data standards, data management or eDC design
Advanced degree in life sciences, computer science or equivalent experience
Strong CDISC, CDASH, SDTM, metadata and CRF design expertise
Experience leading complex studies and cross-functional projects
Knowledge of regulatory submissions and validation tools
Posting record
Report an errorActively hiringFirst seen by us 3 days ago, still listed, and not a repost of an earlier posting.
- Status in our records
- Live
- First seen by us
- Nov 10, 20263 days ago
- Recorded sightings
- 4
- Last seen by us
- Nov 13, 2026
- Employer says posted
- Oct 16, 2026
These dates show when we found the posting. Check the employer’s website to confirm it is still accepting applications.
How this job compares
Emdgroup is hiring
30 open jobs
Open jobs by the week we first saw them, last 12 weeks.
Hiring recordSee how this role fits your experience
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Your next step
Complete your application on careers.emdgroup.com. The employer’s form will show what is required.
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Has Emdgroup posted this job before?
Yes. We’ve followed 2 other Senior Data Standards Expert jobs there since November 2026. All 2 are still up.
Demand for Data Governance roles
New Data Governance postings at the employers we follow are up 170% over the last 6 weeks compared with the 6 before.
Each bar is one week of new postings. The darkest bars are the last 6 weeks.
Counted from the hiring pages we’ve followed for at least five weeks, so employers we add don’t look like growth. Updated weekly.
About the role
We file this job under Data Governance, by the work the posting describes.
Data governance staff keep a company's data accurate, documented and used within the rules. They agree what key fields mean, set up quality checks, track who owns each dataset and look after master data.
Postings ask for SQL, a governance tool such as Collibra or Informatica, knowledge of privacy and data rules, and a lot of work with other teams.
A data engineer builds the systems that move data; governance staff set and check the standards that data has to meet.
Job description
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Your role: In your role as Senior Data Standards Expert / CRF Designer (all genders), you will shape and maintain clinical data standards and design high-quality electronic case report forms for global clinical studies. You will lead complex study builds in electronic data capture systems, manage metadata and standards libraries, and ensure alignment with CDISC, CDASH and SDTM requirements. You will oversee standards deliverables from external partners, support submission readiness, manage study-level standards exceptions, and apply quality-by-design principles. Working across clinical data management, programming, regulatory and technology teams, you will mentor colleagues and drive improvements in standards governance, automation and emerging data formats.
This role requires to be on-site in our office 3 days per week.
Who you are:
- Advanced degree in life sciences, computer science or equivalent experience
- 6 - 8 years in clinical data standards, data management or eDC design
- Strong CDISC, CDASH, SDTM, metadata and CRF design expertise
- Experience leading complex studies and cross-functional projects
- Knowledge of regulatory submissions and validation tools
- Clear communication, problem-solving and mentoring skills
YOUR MAIN BENEFITS:
- Health and well-being: Get access to private medical care, life insurance, and sports card, receive prepaid lunch card
- Work-Life balance: Enjoy additional paid days off, flexible working hours.
- Learning and Development: Take advantage of co-financing for language courses, trainings, and certifications as well as other development opportunities
- Employee support and engagement: Benefit from Employee Assistance Program and join employee engagement groups for support and connection.
Information on how we process your personal data for recruitment purposes, you can find on the registration form in our Recruitment Portal.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
Source details
Source notes
Source excerptsSelected passages from the saved posting. Check the full description for conditions and exceptions.
- Pay
No pay amount identified in the saved description.
- Location & working pattern
Bangalore, Karnataka, India
Your role: In your role as Senior Data Standards Expert / CRF Designer (all genders), you will shape and maintain clinical data standards and design high-quality electronic case report forms for global clinical studies. You will lead complex study builds in electronic data capture systems, manage metadata and standards libraries, and ensure alignment with CDISC, CDASH and SDTM requirements. You will oversee standards deliverables from external partners, support submission readiness, manage study-level standards exceptions, and apply quality-by-design principles. Working across clinical data management, programming, regulatory and technology teams, you will mentor colleagues and drive improvements in standards governance, automation and emerging data formats. This role requires to be on-site in our office 3 days per week. Who you are:
- Work authorization
No clear work-authorization passage found. Eligibility is unconfirmed.