Fortrea Hiring Associate Clinical Data Manager – Apply Now
- Fortrea Hiring Associate Clinical Data Manager in Bangalore
- Company Overview
- Job Role & Responsibilities
- Associate Clinical Data Manager Responsibilities
- Technical Skills Required
- Eligibility / Qualifications
- Educational Qualification
- Experience Requirement
- Location & Salary
- Location
- Estimated Salary
- Application Process
- Apply Online
- Job ID
- Application Deadline
- Work Environment
- Frequently Asked Questions (FAQs)
- 1. What role is Fortrea hiring for in Bangalore?
- 2. What experience is required for this clinical research role?
- 3. Which qualifications are eligible for this role?
- 4. Is Electronic Data Capture (EDC) experience required?
- 5. What is the salary range for this position?
- 6. What is the work location for this opportunity?
- Summary Table
Fortrea Hiring Associate Clinical Data Manager in Bangalore
Fortrea has announced a new hiring opportunity for the role of Associate Clinical Data Manager at its Bangalore location. The company is looking for experienced clinical data management professionals with expertise in sponsor management, clinical trial operations, biometrics, and electronic data capture systems.
This recruitment drive is attracting professionals searching for clinical data management jobs in Bangalore, CRO jobs in India, clinical research data manager vacancies, pharmacovigilance and biometrics careers, EDC specialist jobs, healthcare analytics roles, and sponsor management opportunities in clinical research organizations.
Candidates with strong experience in clinical trial data management, database lock activities, clinical operations, data validation, and sponsor communication will find strong career opportunities through this opening.
Company Overview
Fortrea is a global clinical research organization providing clinical development, laboratory, and healthcare research services across multiple therapeutic and scientific domains. The company supports pharmaceutical, biotechnology, and healthcare organizations with clinical trial management, biometrics operations, pharmacovigilance support, and clinical data management solutions.
The organization operates in highly regulated healthcare and pharmaceutical environments and focuses on delivering data-driven clinical research services aligned with international quality standards and regulatory compliance systems.
Clinical data management continues to remain one of the most critical functions within the pharmaceutical and CRO industry due to increasing demand for accurate clinical trial reporting, healthcare analytics, regulatory compliance, and electronic data management systems.
Bangalore remains one of India’s leading clinical research and healthcare technology hubs, offering significant career opportunities in clinical operations, pharmacovigilance, biometrics, healthcare analytics, medical data review, and sponsor management.
Job Role & Responsibilities
Associate Clinical Data Manager Responsibilities
Candidates selected for this role will lead clinical data management activities from study start-up to database lock while ensuring compliance with sponsor requirements and project timelines.
Key responsibilities include:
- Managing clinical data management activities for assigned studies
- Leading study-related DM operations from start-up to database lock
- Supporting project documentation and system setup activities
- Managing data entry and validation procedures
- Coordinating with sponsors to understand project requirements
- Handling sponsor communication and customer concerns
- Supporting budget and scope management activities
- Reviewing study timelines and project deliverables
- Leading internal data-focused project meetings
- Coordinating with EDC Design, SAS Programming, Statistics, and PK teams
- Managing risk mitigation and database lock timelines
- Ensuring compliance with GCP, SOPs, and regulatory standards
- Supporting reconciliation of clinical databases with safety and laboratory data
- Reviewing client-specific processes and workflow optimization
- Supporting audits and resolving compliance-related observations
- Providing mentorship and guidance to junior team members
- Maintaining accurate project documentation and study records
Technical Skills Required
Candidates should possess knowledge and experience in:
- Clinical Data Management (CDM)
- Electronic Data Capture (EDC)
- Clinical trial operations
- Biometrics and healthcare analytics
- Database lock procedures
- Data validation and reconciliation
- Sponsor management
- Scope and budget management
- GCP and SOP compliance
- Medical terminology
- SAS coordination and reporting workflows
- Clinical database management systems
Professionals with exposure to global CRO environments, healthcare technology platforms, clinical operations management, and regulated pharmaceutical research systems will have an advantage.
Eligibility / Qualifications
Educational Qualification
Candidates with healthcare, life sciences, and technology-related educational backgrounds are eligible.
Relevant educational qualifications include:
B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Clinical Research, Biotechnology, Microbiology, Health Sciences, Information Technology, Clinical Data Management, Healthcare Analytics.
Candidates with scientific and healthcare-related educational backgrounds are preferred.
Experience Requirement
- 6–8 years of clinical data management experience
- Minimum 1 year of direct sponsor management experience
- Experience handling customer concerns preferred
- Experience managing project scope and budgets preferred
- Minimum 3 years of Electronic Data Capture (EDC) experience preferred
These openings are suitable for:
- Clinical Data Managers
- Clinical research professionals
- Biometrics specialists
- EDC professionals
- Sponsor management professionals
- Healthcare analytics specialists
- Clinical operations experts
- CRO industry professionals
Location & Salary
Location
Bangalore / Remote
Estimated Salary
₹12 LPA – ₹22 LPA approximately
Salary may vary depending on sponsor management expertise, CRO experience, EDC exposure, clinical trial management knowledge, and healthcare analytics skills.

Application Process
Interested candidates can apply through the official Fortrea career portal.
Apply Online
https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/Associate-Clinical-Data-Manager_261572
Job ID
261572
Application Deadline
31 May 2026
Work Environment
- Office and home-based work environment
- Flexible shifts as per business requirements
- Overtime and weekend work may be required
Frequently Asked Questions (FAQs)
1. What role is Fortrea hiring for in Bangalore?
Fortrea is hiring for the position of Associate Clinical Data Manager.
2. What experience is required for this clinical research role?
Candidates should have 6–8 years of clinical data management experience with at least 1 year of sponsor management experience.
3. Which qualifications are eligible for this role?
Candidates with qualifications in Pharmacy, Life Sciences, Clinical Research, Healthcare Analytics, Biotechnology, and related disciplines can apply.
4. Is Electronic Data Capture (EDC) experience required?
Yes. Candidates with at least 3 years of EDC experience are preferred.
5. What is the salary range for this position?
The estimated salary range is approximately ₹12 LPA to ₹22 LPA depending on experience and technical expertise.
6. What is the work location for this opportunity?
The position is based in Bangalore with remote or hybrid work flexibility.
Summary Table
| Company | Fortrea |
|---|---|
| Department Vacancies | Associate Clinical Data Manager |
| Qualification | B.Pharm, M.Pharm, Pharm.D, Biotechnology, Life Sciences, Clinical Research, Healthcare Analytics |
| Experience | 6–8 Years Clinical Data Management Experience |
| Location | Bangalore / Remote |
To apply for this job please visit fortrea.wd1.myworkdayjobs.com.