Fortrea Is Hiring for Clinical Research Associate II (Oncology)

Fortrea, a leading global Contract Research Organization (CRO) with over 19,000 employees across 90+ countries, is hiring a Clinical Research Associate II (CRA II) with oncology experience for its operations in Gurugram, with job responsibilities also covering Bangalore.

With three decades of expertise in clinical development across 20+ therapeutic areas, including oncology, Fortrea is committed to accelerating life-changing therapies. This role offers a chance to drive clinical excellence in a dynamic, technology-enabled environment.

Why Fortrea?

Fortrea’s operations in Gurugram and Bangalore support innovative clinical trials for global biopharma clients, leveraging advanced solutions like the INTIENT platform. Employee reviews on Indeed rate Fortrea 3.0/5 for work-life balance, with a 5.0/5 rating for CRA roles, though feedback highlights high turnover and limited raises.

Salaries for CRAs average ₹6-8 Lakhs/year in India, with Fortrea offering competitive pay and benefits like health insurance and 25 days of vacation. Join a collaborative team focused on scientific rigor and patient-centric innovation in oncology trials.

Job Details

Position: Clinical Research Associate II (Job ID: 253728)
Location: Gurugram, Karnataka (with responsibilities in Bangalore)
Type: Full-time, On-site (60% travel required)
Category: Clinical
Experience: Minimum 3 years in clinical monitoring, with oncology experience

Responsibilities

• Conduct site monitoring (Pre-study, Site Initiation, Routine Monitoring, Close-out Visits) per Fortrea SOPs, ICH-GCP guidelines, and sponsor requirements
• Verify study training records, informed consent procedures, and protocol adherence
• Ensure data integrity through source document review, 100% source data verification, and query resolution
• Maintain accurate Investigational Product (IP) inventory and accountability
• Prepare and submit timely trip reports and monitoring visit reports in CTMS
• Track and follow up on Serious Adverse Events (SAEs) and ensure timely reporting
• Support site audit readiness and maintain eTMF/sponsor documents
• Assist with investigator recruitment, training, and study-specific monitoring plans
• Act as a Lead CRA or Local Project Coordinator when assigned
• Collaborate with study teams to meet critical timelines and deliverables

Requirements

• Qualification: University/college degree or certification in a related allied health profession (e.g., nursing licensure); equivalent experience accepted
• Experience:
  • Minimum 3 years of clinical monitoring experience, including oncology trials
  • Familiarity with ICH-GCP, local regulatory requirements, and SAE reporting
• Skills:
  • Proficient in eCRF review, CTMS, and e-clinical systems
  • Strong understanding of clinical trial processes and medical terminology
  • Excellent planning, organization, and problem-solving abilities
  • Ability to work independently with minimal supervision
  • Fluent in English (written and verbal)
• Preferred:
  • Phase I monitoring experience
  • Knowledge of Fortrea SOPs and oncology-specific protocols
  • Experience with USFDA/EMA-regulated trials

Physical Demands/Work Environment

• 60% travel (air and ground) to study sites
• Prolonged computer use (up to 8 hours/day)
• Standard office and clinical site environments
• Potential for non-standard hours based on study needs

How to Apply

• Online: Apply via Fortrea Careers using Job ID: 253728
• Documents: Submit updated CV, educational certificates, experience letters, and certifications (e.g., CPC, nursing licensure)

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🔗Apply Here

Note: Candidates must not have interviewed with Fortrea in the last 6 months. Immediate joiners are preferred. Fortrea does not charge recruitment fees. Contact careers@fortrea.com for queries.

Why a Career with Fortrea?

India’s clinical research market is growing at a 12% CAGR, driven by its role in global trials (Invest India). Fortrea’s oncology focus, highlighted by collaborations like NSCLC biomarker studies, offers exposure to cutting-edge research.

With a 10-year partnership in oncology trials and a collaborative culture, this role provides hands-on experience in high-impact studies, supported by robust training and career development.

Contact Us

Visit Fortrea Careers or email careers@fortrea.com for more details. Join Fortrea to shape the future of oncology clinical research!