Clinical Research Associate II Opening at Fortrea

Fortrea Hiring Clinical Research Associate II in Bangalore | CRA Jobs for Life Science & Nursing Professionals

Fortrea is hiring for the position of Clinical Research Associate II (CRA II) at its Bangalore location. Candidates with experience in clinical monitoring, site management, clinical trial operations, GCP compliance, and healthcare research coordination can apply for this opportunity.

This opening is suitable for professionals searching for CRA jobs in Bangalore, clinical research associate jobs in India, clinical trial monitoring careers, pharmaceutical clinical operations roles, and CRO industry opportunities.

The global clinical research and healthcare outsourcing industry continues to generate strong hiring demand for Clinical Research Associates, site monitoring specialists, clinical operations professionals, and GCP compliance experts. Pharmaceutical companies and Contract Research Organizations (CROs) are actively recruiting professionals with expertise in clinical trial monitoring, patient safety, source data verification, regulatory compliance, and site management.

Candidates with clinical monitoring experience, ICH GCP knowledge, SAE reporting understanding, and exposure to eClinical systems will find this Fortrea opportunity highly relevant for career growth in the clinical research industry.

Company Overview

Fortrea is a globally recognized Contract Research Organization (CRO) specializing in clinical development, healthcare research services, pharmaceutical operations, and clinical trial management solutions. The company supports pharmaceutical, biotechnology, and medical device organizations through advanced clinical research services and operational excellence.

Fortrea provides services across clinical trial management, patient safety, regulatory operations, clinical monitoring, data management, and healthcare technology systems.

The organization offers career opportunities in clinical research, pharmacovigilance, site monitoring, healthcare analytics, regulatory affairs, and pharmaceutical development.

Candidates joining Fortrea gain exposure to global clinical trial operations, international regulatory standards, GCP compliance frameworks, eClinical systems, and healthcare research processes.

Job Role & Responsibilities

Clinical Research Associate II Responsibilities

The selected candidate will manage clinical study monitoring activities, site coordination, patient safety verification, regulatory compliance, and clinical operations responsibilities according to ICH GCP guidelines and sponsor requirements.

Key responsibilities include:

• Conduct clinical site monitoring activities for clinical trials
• Perform Pre-Study, Site Initiation, Routine Monitoring, Process Monitoring, and Close-Out Visits
• Verify informed consent procedures and protocol compliance
• Ensure patient safety and protection throughout study activities
• Review source documents and perform source data verification (SDV)
• Generate and resolve data queries using clinical data management systems
• Maintain site regulatory documents and eTMF records
• Track investigational product inventory and accountability
• Ensure audit readiness and compliance at site level
• Prepare and implement clinical monitoring plans
• Submit accurate monitoring and trip reports
• Support SAE tracking and follow-up activities
• Coordinate with investigators, study teams, and project stakeholders
• Assist in clinical project administration and investigator documentation
• Use CTMS and eClinical systems for trial management activities
• Present training content during site initiation visits
• Support training of new clinical operations employees
• Ensure adherence to ICH GCP guidelines and regulatory requirements

This role is suitable for candidates searching for:

• Clinical Research Associate jobs in Bangalore
• CRA II jobs in CRO companies
• Clinical monitoring jobs in pharma companies
• Site management associate careers
• Clinical trial operations jobs
• GCP compliance specialist jobs
• Clinical research monitoring careers
• Pharmaceutical clinical operations roles
• Healthcare research coordinator jobs
• CRO industry clinical jobs

Eligibility / Qualifications

Educational Qualification

Candidates with the following educational backgrounds are eligible: B.Pharm, M.Pharm, Pharm.D, BSc Nursing, MSc Nursing, Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Allied Health Sciences, Medical Laboratory Technology, and related healthcare or life science degrees.

Candidates with equivalent clinical monitoring experience may also be considered.

Experience

Candidates should have:

• Minimum 2 years of clinical monitoring experience
• Experience in clinical trial site monitoring and management
• Knowledge of ICH GCP guidelines and local regulatory requirements
• Experience working with eClinical systems and CTMS platforms
• Understanding of SAE reporting and clinical trial documentation

Required Skills

Applicants should possess:

• Strong knowledge of clinical monitoring procedures
• Understanding of clinical trial processes and regulatory compliance
• Good analytical and problem-solving abilities
• Strong documentation and reporting skills
• Knowledge of source data verification and eCRF review
• Good communication and interpersonal skills
• Ability to work independently and within matrix teams
• Understanding of medical and clinical research terminology
• Good organizational and planning abilities
• Proficiency in Microsoft Office applications and clinical systems
• Attention to detail and quality compliance understanding

Preferred Skills

Candidates with the following experience may have an added advantage:

• Phase I clinical monitoring experience
• Medical device clinical trial exposure
• Technical writing or data management experience
• Experience in healthcare research operations
• Additional clinical operations exposure

Location & Salary

Job Location

Bangalore

Work Environment & Travel

• Standard office and clinical site environment
• Travel Requirement: Approximately 60%
• Site visits and hospital visits required

Expected Salary

₹8 LPA to ₹14 LPA approximately, depending on CRA experience, clinical monitoring expertise, therapeutic area exposure, and interview performance.

Application Process

Interested candidates can apply directly through the official Fortrea careers portal using the link below:

Apply Here: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/Clinical-Research-Associate-II_262282

Candidates are advised to apply early as Clinical Research Associate positions at multinational CRO companies receive a high number of applications.

Frequently Asked Questions

Who can apply for the Fortrea Clinical Research Associate II role?

Candidates from Pharmacy, Nursing, Life Sciences, Biotechnology, Clinical Research, and Allied Health backgrounds with clinical monitoring experience can apply.

What experience is required for this CRA II position?

Candidates should have at least 2 years of clinical monitoring experience along with knowledge of ICH GCP guidelines.

What is the expected salary for CRA II jobs in Bangalore?

The estimated salary range for Clinical Research Associate II roles is approximately ₹8 LPA to ₹14 LPA.

Is travel required for this clinical research role?

Yes. The position involves approximately 60% travel for site monitoring and clinical trial visits.

What systems are commonly used in this role?

Candidates may work with CTMS, eClinical systems, eTMF platforms, and clinical data management systems.

What are the major responsibilities of a Clinical Research Associate II?

The role includes clinical monitoring, source data verification, patient safety review, regulatory compliance, site management, and trial documentation activities.

Company	Fortrea
Department Vacancies	Clinical Research Associate II
Qualification	B.Pharm, M.Pharm, Pharm.D, Nursing, Life Sciences, Clinical Research
Experience	Minimum 2 Years Clinical Monitoring Experience
Location	Bangalore