Fortrea is inviting applications for the position of Central Monitoring Associate Manager in Bangalore. This is a full-time opportunity for experienced clinical research professionals with a strong background in clinical trials, central monitoring, data management, project management, or informatics.
The role focuses on the execution and oversight of central monitoring activities across multiple studies and customers. The selected professional will work with cross-functional teams and key stakeholders to review study, site, and subject-level data, identify potential risks, recommend mitigation actions, and support effective clinical trial oversight.
Candidates with a university or college degree and 6–8 years of relevant clinical research experience can apply. Experience in a pharmaceutical company, CRO, or equivalent clinical trial environment is required.
Fortrea Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Fortrea |
| Position | Central Monitoring Associate Manager |
| Job Requisition ID | 264910 |
| Location | Bangalore |
| Job Type | Full Time |
| Experience | 6–8 Years |
| Qualification | University / College Degree |
| Industry Experience | Pharmaceutical / CRO / Clinical Research |
| Travel Requirement | Global, approximately 15% |
| Application Deadline | 30 October 2026 |
About Fortrea
Fortrea is a clinical research organization that supports clinical development and research programs across the life sciences industry.
The Central Monitoring Associate Manager position supports clinical trial oversight through centralized data review, risk assessment, analytics, monitoring strategies, and informatics platforms. The role works closely with study teams and clients to help ensure that monitoring activities are conducted effectively and according to defined study plans.
Job Description
The Central Monitoring Associate Manager is responsible for carrying out key central monitoring activities across assigned studies. The role can involve site-, subject-, and study-level reviews, depending on the applicable monitoring plan.
The professional will collaborate across functions and work with internal teams, sponsors, and other stakeholders to identify risks, review data, communicate findings, and recommend appropriate mitigation measures.
The position also provides technical leadership in the implementation of central monitoring processes and related tools. Depending on responsibilities assigned, the role may also include line-management duties for Central Monitoring or Medical Data Review Operations staff.
Central Monitoring Associate Manager
The role involves overseeing central monitoring activities from the implementation of the informatics platform through study reporting and closeout. The successful candidate should be comfortable working with clinical trial data, risk-based monitoring concepts, analytics, and cross-functional study teams.
Eligibility Criteria
Candidates should meet the following requirements:
- University or college degree from an appropriately accredited institution.
- 6–8 years of relevant clinical research experience.
- Experience in a pharmaceutical company, CRO, or equivalent clinical research environment.
- Increasing levels of responsibility in clinical trial-related roles such as:
- Project management.
- Clinical monitoring.
- Data management.
- Informatics.
- Ability to work collaboratively with multiple stakeholders.
- Understanding of broader drug development and clinical trial processes.
Fortrea may consider relevant and equivalent professional experience in place of the stated educational requirement.
Preferred Qualifications
- Post-graduation in Life Sciences or another applicable field.
- Relevant additional qualifications and professional experience related to clinical research and central monitoring.
Skills and Qualifications
The role requires strong technical, analytical, and communication capabilities, including:
- Knowledge of clinical research and clinical trial processes.
- Central monitoring and risk-based monitoring knowledge.
- Ability to interpret study, site, and subject-level information.
- Data-driven analytical and decision-making skills.
- Understanding of clinical data and monitoring strategies.
- Ability to work with informatics platforms and monitoring tools.
- Strong stakeholder communication skills.
- Ability to identify risks and recommend appropriate mitigation actions.
- Strong project coordination and organizational abilities.
- Ability to manage multiple studies and customer requirements.
- Technical leadership and problem-solving capabilities.
- Ability to work effectively in a matrix organization.
Key Responsibilities
The Central Monitoring Associate Manager may be responsible for:
- Performing central monitoring activities across multiple studies.
- Tracking study progress and providing accurate status reports.
- Acting as a lead for central monitoring teams across multiple studies and customers.
- Supporting managers and leadership with study risk assessments.
- Supporting sponsor presentations and bid-defense activities.
- Contributing to Risk Assessment and Categorization Tool (RACT) activities related to central monitoring and medical reviews.
- Supporting data experts with critical data and process definitions and EDC design implementation.
- Contributing to informatics platform requirements and visualization design.
- Considering study data feeds such as EDC and laboratory data when developing platform requirements.
- Defining study-specific risk factors and trigger levels.
- Supporting SDV strategy and risk-factor mitigation planning.
- Preparing and maintaining configuration and other applicable study plans.
- Updating plans as the study’s risk profile and requirements evolve.
- Configuring monitoring tools and testing variable risk factors.
- Adjusting trigger levels and central monitoring parameters as required.
- Conducting ongoing data reviews and recommending mitigation actions.
- Reviewing monitoring levels with project teams and following identified issues through resolution.
- Recommending changes to monitoring intervention levels based on study strategies and emerging risks.
- Preparing and distributing project or study reports during study conduct and at closeout.
- Performing site-, subject-, and study-level central monitoring activities as applicable.
- Supporting inspection readiness and regulatory authority inspections when required.
- Reviewing subject-level findings and coordinating their resolution with relevant stakeholders.
- Conducting study analytics reviews according to applicable plans.
- Communicating analytical findings to key stakeholders.
- Preparing Project Quality and Risk Reports during the study and at closeout.
- Performing specialized reviews of central data review tools based on relevant clinical, data, or statistical expertise.
- Identifying potential study scope and risk-profile changes.
- Providing technical leadership to study teams for effective process and tool implementation.
- Evaluating process improvement suggestions and submitting recommendations to leadership.
- Identifying opportunities to improve systems and monitoring tools.
- Supporting efforts to position central monitoring and informatics capabilities with clients.
Line Management Responsibilities
Where the position includes line-management responsibilities, the role may also involve:
- Training and developing Central Monitoring or Medical Data Review Operations staff.
- Allocating and classifying employee tasks.
- Supervising and mentoring team members.
- Evaluating employee performance and competency development.
- Supporting career development and interpersonal skill development.
- Addressing workforce HR requirements.
- Assisting with recruitment activities.
- Supporting workforce budgeting and scheduling.
- Ensuring smooth departmental operations.
- Managing performance reviews and issues involving direct reports.
Work Location and Travel Requirements
The position is based in Bangalore and is offered as a full-time role.
The job posting indicates that standard office or home-working equipment is required.
Travel Requirement: Global travel
Expected Travel: Approximately 15%
Salary / CTC
Fortrea has not specified the salary or CTC for the Central Monitoring Associate Manager position in the provided job posting. Candidates should refer to the official recruitment communication for compensation details.
Selection Process
The detailed selection stages have not been specified in the provided vacancy information. Eligible candidates can submit their application through the official Fortrea careers portal and follow further instructions provided during the recruitment process.
How to Apply for Fortrea Recruitment 2026
Interested and eligible candidates can apply online through the official Fortrea careers portal.
Position: Central Monitoring Associate Manager
Job Requisition ID: 264910
Location: Bangalore
Job Type: Full Time
Application Deadline: 30 October 2026
Candidates should review the job requirements carefully and ensure that the information submitted in their application is accurate and complete.
Important Details Before Applying
- Company: Fortrea
- Position: Central Monitoring Associate Manager
- Requisition ID: 264910
- Location: Bangalore
- Job Type: Full Time
- Experience: 6–8 Years
- Qualification: University / College Degree
- Preferred Qualification: Post-graduation in Life Sciences
- Industry Experience: Pharmaceutical / CRO / Clinical Research
- Travel: Global, approximately 15%
- Application Deadline: 30 October 2026
- Application Mode: Online
Important Note
Candidates should carefully verify their qualifications and relevant clinical research experience before applying. Vacancy status, deadlines, recruitment requirements, and other job details may change. Applicants are advised to check the latest information on the official Fortrea careers portal before submitting their application.
FAQs – Fortrea Recruitment 2026
1. What position is Fortrea hiring for?
Fortrea is hiring for the position of Central Monitoring Associate Manager.
2. Where is this Fortrea job located?
The position is based in Bangalore.
3. What educational qualification is required?
A university or college degree from an appropriately accredited institution is required. Relevant and equivalent experience may be considered in lieu of the educational requirement.
4. How much experience is required?
Candidates should have 6–8 years of relevant clinical research experience in a pharmaceutical company, CRO, or equivalent environment.
5. Is a Life Sciences postgraduate degree preferred?
Yes. Post-graduation in Life Sciences or another applicable qualification is listed as preferred.
6. What does a Central Monitoring Associate Manager do?
The role involves central monitoring of clinical studies, study and risk assessment activities, data and analytics reviews, monitoring-plan development, risk mitigation, reporting, stakeholder communication, and technical support for monitoring tools and processes.
7. Is travel required for this position?
Yes. The job posting specifies global travel of approximately 15%.
This version keeps the technical scope, experience requirements, responsibilities, travel details, and application deadline aligned with the supplied Fortrea posting.