Fortrea is hiring for the position of Central Monitor Assistant in Bangalore. The vacancy is listed as a full-time opportunity and involves providing operational, administrative and technical support to clinical study teams.
This role may be relevant to candidates with a background in Life Sciences or an allied health profession and around 2–3 years of experience in clinical research. The position involves clinical trial systems, study documentation, data review, investigator payments, site start-up support and other study management activities.
Fortrea Recruitment 2026 – Job Highlights
| Job Detail | Information |
|---|---|
| Company Name | Fortrea |
| Job Title | Central Monitor Assistant |
| Job ID / Requisition ID | 262504 |
| Job Location | Bangalore |
| Employment Type | Full time |
| Experience | 2–3 years in clinical research/job discipline |
| Preferred Qualification | University/College Degree in Life Science |
| Language Requirement | Fluent English, written and verbal |
About the Company
Fortrea provides services supporting clinical development and research programs. Its teams work on activities related to clinical studies, including study operations, documentation, data and site support.
The Central Monitor Assistant position supports study teams with clinical systems, documentation, reporting, data review, investigator payments and other operational activities throughout the study lifecycle.
Job Description
The Central Monitor Assistant will provide day-to-day support to clinical study teams and assist with a range of study-related processes. The work includes managing access to clinical systems, maintaining study databases, supporting electronic Trial Master File (eTMF) activities and preparing study reports.
The role also includes data review support, investigator payment processing, document management, site start-up assistance and coordination with different study team members.
Central Monitor Assistant
The position combines clinical trial administration with technical and operational study support. The selected candidate will be expected to maintain accurate documentation, follow established procedures, complete assigned activities within timelines and escalate issues when necessary.
The role may involve working with systems such as CTMS, IWRS and EDC, along with supporting study teams during start-up, ongoing study activities and close-out.
Eligibility / Educational Qualification
Candidates should meet the following requirements:
- University or college degree, preferably in Life Sciences.
- Alternatively, certification in an allied health profession from an appropriate accredited institution may be considered, such as nursing, medical technology or laboratory technology.
- Around 2–3 years of work experience in clinical research.
- Strong working knowledge of ICH-GCP guidelines and other applicable guidelines and regulations.
- Fluent English communication skills, both written and verbal.
- Fortrea may consider relevant and equivalent professional experience in place of the stated educational requirements.
Skills and Qualifications
Candidates should demonstrate:
- Ability to organize work effectively.
- Strong written and verbal communication skills.
- Good attention to detail.
- Ability to collaborate effectively with other team members.
- Ability to consistently deliver high-quality work.
- Ability to use computers and relevant departmental tools.
- Familiarity with clinical research processes and applicable guidelines.
- Ability to manage documentation and study-related information accurately.
- Ability to follow established procedures and work within required timelines.
Key Responsibilities
The Central Monitor Assistant may be responsible for:
- Managing clinical systems and user access as required for assigned studies.
- Maintaining study databases, including CTMS, IWRS and EDC systems.
- Supporting study teams with eTMF management activities.
- Assisting with study data review and related support activities.
- Preparing and generating study-specific reports.
- Following up with Clinical Research Associates (CRAs) regarding outstanding issues and action items.
- Supporting the study lead with study-specific data review activities.
- Setting up study systems for newly awarded studies.
- Supporting CTMS compliance management.
- Coordinating project communications.
- Assisting project teams with additional study support activities.
- Reviewing EDC and contract information for investigator payment processing.
- Marking applicable CTMS line items as ready for payment or screen failure.
- Working with the appropriate payment team to generate cover letters or proforma invoices and payment batches in CTMS.
- Performing invoice quality-control checks and preparing GIA where applicable.
- Coordinating with Clinical Trial Leads and Project Managers for line-item and GIA approvals.
- Processing out-of-pocket and pass-through expense invoices.
- Performing payment reconciliation during study close-out or when requested by the study team.
- Following applicable departmental SOPs and Work Instructions.
- Completing required training within specified timelines.
- Managing daily responsibilities while maintaining quality and productivity.
- Maintaining project and technical documentation appropriately.
- Providing administrative and technical assistance to internal departments and teams.
- Performing quality checks on completed work.
- Escalating issues and supporting timely resolution when required.
- Tracking and reporting management-defined metrics within required timelines.
- Supporting the implementation of revised processes and procedures.
- Assisting with document management, including template creation, document collection, review, processing, tracking and eTMF filing.
- Supporting document-related activities throughout the study duration within the agreed scope.
- Assisting with preparation of new investigator submission packages for site and regulatory submissions.
- Supporting investigator payment processing.
- Assisting study and start-up teams with activities required for site initiation and start-up.
- Supporting assigned studies with document uploads according to defined objectives.
- Following up with study teams regarding document-upload queries.
- Reviewing and supporting the management of site clinical trial contracts according to defined processes and timelines.
- Creating an iSite Pack.
- Performing other duties assigned by the study management team.
Work Location and Shift Details
The Central Monitor Assistant position is based in Bangalore and is listed as a full-time opportunity.
The available job information does not specify working hours, shift timings or whether the position follows a remote or hybrid arrangement.
Salary / CTC
Salary details have not been specified in the available job information. Candidates should refer to the official Fortrea careers portal or employer communication for compensation details.
Selection Process
The exact selection process, interview rounds and assessment procedure have not been provided in the available job information. Candidates should follow the recruitment instructions communicated by Fortrea during the application process.
Benefits / Career Opportunities
The available vacancy information does not specify particular employment benefits, bonuses, insurance coverage, transportation facilities or other monetary perks for this position.
The role does provide exposure to clinical research operations, study systems, documentation, data review, investigator payments, site start-up and other clinical trial support activities.
How to Apply
Eligible candidates can apply for the Central Monitor Assistant position through the official Fortrea careers portal.
The Job Requisition ID is 262504. Candidates should review the requirements carefully and submit complete and accurate information as part of the application.
The listed application deadline is September 30, 2026.
Important Details Before Applying
- Company: Fortrea
- Position: Central Monitor Assistant
- Location: Bangalore
- Qualification: University/College Degree, preferably in Life Sciences, or eligible allied health certification
- Experience: 2–3 years in clinical research
- Job Type: Full time
- Work Mode: Not specified
- Shift: Not specified
- Job ID: 262504
- Application Deadline: September 30, 2026
Important Note
Job availability, deadlines, eligibility requirements and recruitment conditions may change. Candidates should verify the latest information on Fortrea’s official careers website before applying. The company may also consider relevant equivalent experience in place of the stated educational requirements.
FAQs
Who can apply for the Fortrea Central Monitor Assistant job?
Candidates with a university or college degree, preferably in Life Sciences, or an appropriate allied health certification can be considered. The position also requires around 2–3 years of clinical research experience and knowledge of ICH-GCP and applicable regulations.
What qualification is required for this Fortrea job?
A university or college degree is preferred, particularly in Life Sciences. Certification in an allied health profession, such as nursing, medical technology or laboratory technology, may also qualify. Fortrea may consider relevant equivalent experience instead of the educational requirement.
How much experience is required?
The vacancy specifies 2–3 years of experience in clinical research. It also lists 2–3 years of experience in the job discipline and up to 3 years of experience in other professional roles.
Where is the Central Monitor Assistant job located?
The position is located in Bangalore.
Is the Fortrea Central Monitor Assistant position remote?
The available job information does not specify a remote or hybrid work arrangement. The vacancy is listed for Bangalore.
What is the application deadline?
The listed application deadline is September 30, 2026. Candidates should check the official Fortrea careers portal for the latest vacancy status before applying.