Clinical Research Associate II Opening at Fortrea

- About Fortrea
- Current Openings
- Educational Background & Relevant Courses
- Key Responsibilities
- Preferred Qualifications & Skills
- How to Apply
- Company & Job Summary Table
Clinical Research Associate II Opening at Fortrea Gurugram | Life Science/Nursing Graduates with 3+ Years Experience
Apply now for CRA II roles at Fortrea Gurugram. Life Science or Nursing graduates with 3+ years of clinical research experience required.
Advance Your Clinical Research Career – Join Fortrea as a CRA II in Gurugram
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📱 Join Click HereLooking to grow in your clinical research career with a global contract research organization? Fortrea is hiring for the role of Clinical Research Associate II in Gurugram, Haryana. This is a high-responsibility, travel-intensive role for experienced CRAs with strong monitoring and regulatory skills.
About Fortrea
Fortrea is a leading CRO offering clinical development solutions across the pharma, biotech, and medical device industries. Known for scientific innovation, Fortrea empowers its professionals with cutting-edge tools, global projects, and a collaborative work culture.
Current Openings
Position: Clinical Research Associate II
- Location: Gurugram, Haryana (Base: Bangalore office)
- Experience: Minimum 3 years in Clinical Monitoring & Oncology Trials
- Required Education: Life Science/Nursing degree or equivalent certification
- Department: Clinical Operations
Educational Background & Relevant Courses
Accepted Qualifications:
- B.Sc./M.Sc. in Life Sciences
- B.Pharm/M.Pharm
- Nursing Licensure or Allied Health Certifications
Relevant Courses:
- Clinical Research & Pharmacovigilance
- ICH-GCP & ISO 14155 Guidelines
- Clinical Data Management
- Adverse Event Reporting
- Trial Monitoring & Regulatory Documentation
Key Responsibilities
- Perform on-site and remote monitoring for clinical trials across phases
- Ensure informed consent and protocol compliance during site visits
- Validate data integrity through Source Data Verification (SDV)
- Maintain updated site regulatory documents and eTMF
- Monitor investigational product inventory and accountability
- Lead site audits and support inspection-readiness
- Update CTMS and generate visit reports accurately and on time
- Mentor junior CRAs and deliver study-specific training at site initiation
Preferred Qualifications & Skills
- Working knowledge of Fortrea SOPs and trial management tools
- Experience with oncology Phase I–III studies
- Strong interpersonal, documentation, and negotiation skills
- Proficiency in CTMS, EDC systems, and Microsoft Office
- Understanding of SAE reporting and follow-up procedures
- Readiness to travel up to 60% of the time

How to Apply
Click below to apply via the official Fortrea careers portal: 👉 Apply Here
🗓️ Last date to apply: 31st July 2025
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Company & Job Summary Table
Company Name | Current Vacancies in Departments | Required Education | Experience Required |
---|---|---|---|
Fortrea | Clinical Research – Monitoring | B.Sc/M.Sc Life Sciences, B.Pharm, Nursing | Minimum 3 years in CRA role |
Step into a pivotal role in global clinical trials. Join Fortrea and contribute to advancing healthcare research.
To apply for this job please visit fortrea.wd1.myworkdayjobs.com.