Fortrea Hiring Clinical Research Associate II (CRA II)
Are you seeking Fortrea Careers Bangalore or a Clinical Trial Monitor Job in India? Leading global Contract Research Organization (CRO) Fortrea is hiring experienced clinical professionals for the position of Clinical Research Associate II (CRA II) (Job ID: 262275) to manage investigator sites.
This clinical operations monitoring vacancy is ideal for life sciences, nursing, or pharmacy graduates with a minimum of 2 years of independent clinical monitoring experience. Selected candidates will verify informed consent compliance, perform source data verification (SDV), track IP records, and manage safety reporting documentation. To draft a resume detailing your SDV metrics or database audit history, read our guidelines on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particular | Details |
|---|---|
| Company | Fortrea (Fortrea Development India Private Limited) |
| Position | Clinical Research Associate II (CRA II) |
| Job ID | 262275 |
| Job Location | Bangalore, Karnataka, India |
| Employment Type | Full-Time |
| Experience Required | 2+ Years (independent clinical monitoring) |
| Qualifications | University degree in Life Sciences, Pharmacy, Nursing, or Allied Health Sciences |
| Travel Requirement | Up to 60% (traveling to investigator sites) |
| Application Deadline | 31 August 2026 |
| Expected Salary | ₹8,00,000 – ₹14,00,000 per annum (Estimated) |
💼 Key Responsibilities
- Site Visits: Conduct pre-study, site initiation, routine monitoring, process monitoring, and close-out visits.
- Source Document Verification: Execute 100% SDV and review electronic Case Report Forms (eCRFs) to verify accuracy.
- Subject Protection: Audit patient screening processes, informed consent signatures, and eligibility criteria.
- Drug Accountability: Check Investigational Product (IP) storage temperature logs, dispensing records, and reconciliation sheets.
- Safety Reporting: Support Serious Adverse Event (SAE) reporting processes, drafting narratives and filing reports.
- Audit Readiness: Maintain on-site regulatory files and eTMF folders in a state of inspection readiness.
To learn how clinical operations and associate monitoring salaries compare to conventional pharmacovigilance drug safety associate and data analytics structures, read our report on Pharmacovigilance Salary: India vs USA.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master’s degree in Pharmacy, Nursing, Life Sciences, or allied healthcare disciplines.
- Core Experience: Minimum 2 years of clinical monitoring experience within a CRO, pharma sponsor, or clinical operations unit.
- Guidelines Knowledge: In-depth working knowledge of ICH-GCP guidelines, local FDA regulations, and trial guidelines.
- eClinical Systems: Working experience with CTMS trackers, eCRFs, and electronic document repositories.
- Language Skills: Good written and verbal English communication to draft detailed monitoring trip reports.
For science graduates evaluating corporate monitoring pathways compared to conventional laboratory quality control or direct dispensing chemist careers, read our analysis on B.Pharm Careers after Graduation: India vs USA.
🎁 Why Join Fortrea?
- Work with a leading global spin-off CRO company managing complex therapeutic pipelines.
- Gain extensive exposure to Phase I-IV trials, multinational sponsors, and investigator network management.
- Opportunity to support Phase I oncology or specialty trial monitoring protocols.
- Attractive travel allowances, competitive compensation, and structured training programs.
To review your basic knowledge of clinical databases, safety protocols, and GCP guidelines before your screening calls, try our interactive Clinical Trial Assistant (CTA) Quiz.
💡 CRA II vs Healthcare IT
Clinical Research Associates conduct site initiation visits, perform source data verification, and track IP compliance, whereas Healthcare IT professionals support software deployments. To explore these differences, read our comparison on Healthcare IT vs Clinical Healthcare.
📝 Resume Tips for Fortrea CRA Candidates
- Quantify Monitoring History: Explicitly state the number of monitoring visits (IMVs, SIVs, COVs) you have conducted.
- Specify Therapeutic Areas: Detail clinical fields (Oncology, Cardiology, Immunology) and trial phases (Phase I-IV) you monitored.
- List eClinical Tools: Name the exact CTMS, EDC, or eTMF systems you are fluent in utilizing.
💬 Fortrea CRA II Interview Questions
- Q1. How do you handle a protocol deviation regarding a missed lab test at a site?
Answer Guidance: I log the deviation in the monitoring report, request the coordinator to document the event, investigate why the test was missed, train the site staff on the protocol requirements, and document preventive steps. - Q2. What are the key elements to verify during Investigational Product (IP) accountability?
Answer Guidance: I verify shipment records, check that storage temperatures match protocol guidelines, compare dispensed counts against patient dosing logs, check return/destruction logs, and verify expiration dates. - Q3. Explain the difference between source document verification (SDV) and source document review (SDR).
Answer Guidance: SDV is the process of comparing data entered in the eCRF against source documents (e.g. lab reports). SDR is a broader review of the quality of source documentation, protocol compliance, investigator involvement, and subject safety.
🚀 How to Apply?
Interested and eligible candidates can submit their applications directly via Fortrea's official Workday careers board. Click the button below to apply:
Apply Online – Fortrea Workday Career Board❓ Frequently Asked Questions
Q. What is the required experience for this Fortrea CRA II opening?
Fortrea requires a minimum of 2 years of active clinical monitoring experience for external candidates.
Q. What is the travel requirement for the CRA II role?
This role involves extensive field monitoring, requiring travel to study sites up to 60% of the time.
Q. What is the application deadline for this position?
Candidates can submit applications through the official Workday portal until 31 August 2026.
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