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Cra Ii / Sr. Cra I (Oncology)

Syneos Health
5+ years
Not Disclosed
PAN-India, India
1 June 3, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

CRA II / Sr. CRA I (Oncology)

Location: India (Client Site)
Work Mode: On-site / Remote Monitoring (as per study requirement)
Department: Clinical Operations / Clinical Monitoring

Job Overview

We are seeking experienced professionals for the role of Clinical Research Associate (CRA II / Sr. CRA I) – Oncology to support clinical trial monitoring activities across oncology studies. This role is responsible for ensuring clinical trial site compliance, patient safety, data integrity, and adherence to regulatory and protocol requirements throughout the study lifecycle.

The position requires strong oncology monitoring experience, hands-on expertise in site management activities, and a solid understanding of ICH-GCP guidelines and global regulatory standards.

Key Responsibilities

Site Monitoring and Management

  • Perform site qualification, site initiation, interim monitoring, and site close-out visits (on-site or remote).

  • Ensure clinical trial sites comply with protocol requirements, SOPs, ICH-GCP guidelines, and applicable regulatory standards.

  • Evaluate overall site performance and provide recommendations for improvement or corrective actions.

  • Identify and escalate critical site issues to project teams promptly.

Patient Safety and Compliance

  • Verify informed consent processes are properly conducted and documented.

  • Ensure subject safety and confidentiality are maintained at all times.

  • Identify protocol deviations, violations, and pharmacovigilance-related issues.

  • Assess risks affecting patient safety and data integrity at investigational sites.

Data Review and Quality Assurance

  • Conduct source document verification (SDV) and review clinical records for accuracy and completeness.

  • Ensure case report form (CRF) data is accurate, complete, and consistent with source data.

  • Perform query generation, resolution, and follow-up within agreed timelines.

  • Support compliance with electronic data capture (EDC) systems and processes.

Investigational Product (IP) Management

  • Perform investigational product accountability, reconciliation, and compliance checks.

  • Verify proper storage, dispensing, and administration of study medication per protocol.

  • Identify and report risks related to blinded or randomized IP information.

  • Ensure compliance with labeling, import, release, and return procedures.

Regulatory Documentation and Trial Master File (TMF)

  • Review Investigator Site Files (ISF) for accuracy, completeness, and timeliness.

  • Ensure alignment between ISF and Trial Master File (TMF).

  • Support proper archiving of essential study documents as per regulatory requirements.

  • Ensure documentation readiness for audits and inspections.

Clinical Operations Support

  • Utilize monitoring plans (CMP/SMP) to guide site activities and compliance checks.

  • Use clinical systems and tools effectively for study conduct and documentation.

  • Maintain knowledge of evolving regulatory guidelines and industry best practices.

Stakeholder Communication

  • Collaborate with investigators, site staff, data management teams, and project stakeholders.

  • Provide guidance to site staff to ensure compliance with study requirements.

  • Communicate study progress, risks, and issues clearly to internal teams.

Required Qualifications

Education

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related discipline.

Experience Required

Fresher Eligible: No

Required Experience: Minimum 5+ years of clinical monitoring experience (CRA role)

  • Strong hands-on experience in Oncology clinical trials is mandatory