Fortrea Central Monitoring Specialist Jobs Apply
- Fortrea Hiring Central Monitoring Specialist in Bangalore | Clinical Research & Risk-Based Monitoring Jobs
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Skills Required:
- Experience:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What kind of work will I be doing?
- What tools are used in this role?
- What is the career growth?
- Is clinical trial experience mandatory?
Fortrea Hiring Central Monitoring Specialist in Bangalore | Clinical Research & Risk-Based Monitoring Jobs
Fortrea is hiring experienced professionals for the role of Central Monitoring Specialist in Bangalore. This is a full-time opportunity in the clinical research and risk-based monitoring domain, ideal for candidates with 3–5 years of experience in clinical trials, data analytics, and study monitoring. The company is offering multiple opportunities for professionals aiming to advance their careers in centralized monitoring, clinical data review, and risk management within global CRO environments.
This role is designed for candidates who want to work on advanced clinical trial analytics, risk-based monitoring strategies, and data-driven decision-making in pharmaceutical and biotechnology studies.
Company Overview
Fortrea is a global contract research organization (CRO) specializing in clinical development, patient access, and technology-driven solutions for the pharmaceutical and biotechnology industries. The company supports end-to-end clinical trial execution, helping accelerate drug development while ensuring compliance with global regulatory standards.
With a strong focus on innovation, informatics platforms, and risk-based monitoring, Fortrea provides professionals exposure to cutting-edge clinical research technologies and global clinical trial operations.
Job Role & Responsibilities
As a Central Monitoring Specialist, you will play a key role in executing centralized monitoring activities across multiple clinical studies. This includes reviewing study data, identifying risks, and supporting data-driven decision-making to improve study quality and compliance.
Key responsibilities include:
- Perform centralized monitoring activities across multiple clinical trials and portfolios
- Review study, site, and subject-level data to identify risks and inconsistencies
- Support development and execution of study risk assessment strategies
- Analyze risk indicators and recommend mitigation actions to project teams
- Prepare and review monthly study risk reports and dashboards
- Coordinate study risk assessment meetings and documentation
- Track study progress and follow up on outstanding queries and site issues
- Work with informatics platforms, including EDC and data visualization tools
- Support User Acceptance Testing (UAT) for clinical systems and tools
- Draft and update central monitoring plans and configuration documents
- Perform subject-level data review and ensure issue resolution
- Communicate findings and insights to internal teams and stakeholders
- Contribute to process improvements and system enhancements
This role directly contributes to improving clinical trial quality, reducing risks, and ensuring compliance with global regulatory requirements.
Eligibility / Qualifications
Candidates must meet the following educational requirements:
BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research, Health Sciences, Bioinformatics
Skills Required:
- Strong understanding of clinical trials and risk-based monitoring
- Knowledge of ICH-GCP guidelines and regulatory compliance
- Experience with EDC systems and clinical data platforms
- Strong analytical and problem-solving skills
- Good project management and organizational abilities
- Effective communication and stakeholder management skills
Experience:
- 3 to 5 years of experience in clinical research, CRO, or pharmaceutical industry
Location & Salary
- Location: Bangalore
- Salary: Competitive salary package as per CRO industry standards
Application Process
Interested candidates can apply through the official Fortrea careers portal:
Apply Here: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/Cental-Monitoring-Specialist_261806-1
Apply before the deadline to secure your chance in this high-demand clinical research role.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, this role requires prior clinical research experience.
What kind of work will I be doing?
You will analyze clinical trial data, identify risks, and support centralized monitoring activities.
What tools are used in this role?
You will work with EDC systems, informatics platforms, and data visualization tools.
What is the career growth?
You can move into roles such as Risk-Based Monitoring Lead, Clinical Project Manager, or Data Analytics Lead.
Is clinical trial experience mandatory?
Yes, experience in clinical trials or related roles is essential.
| Category | Details |
|---|---|
| Company | Fortrea |
| Vacancies | Central Monitoring Specialist |
| Required Education | BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacy, Clinical Research, Health Sciences, Bioinformatics |
| Experience | 3–5 Years |
To apply for this job please visit fortrea.wd1.myworkdayjobs.com.
