Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Cra Ii / Sr. Cra I (Oncology)

Syneos Health
5+ years
INR 12 LPA – 18 LPA
PAN-India, India
1 June 11, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development

CRA II / Sr. CRA I (Oncology)

Company: Syneos Health
Location: Client-Based (India)
Job ID: 25108468
Employment Type: Full-Time
Work Mode: Field-Based / Client Site
Experience: 5+ Years Clinical Monitoring Experience
Therapeutic Area: Oncology (Mandatory)

About the Role

Syneos Health is hiring a CRA II / Sr. CRA I (Oncology) to support clinical trial monitoring activities across oncology studies. The role involves site management, monitoring visits, regulatory compliance, patient safety oversight, data quality review, and collaboration with investigators, sponsors, and study teams to ensure successful study execution.

Key Responsibilities

Clinical Trial Monitoring

  • Perform Site Qualification Visits (SQV), Site Initiation Visits (SIV), Interim Monitoring Visits (IMV), and Close-Out Visits (COV).

  • Ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.

  • Evaluate site performance and identify potential risks or issues.

  • Escalate critical findings and develop corrective action plans.

Patient Safety & Data Integrity

  • Verify informed consent procedures and documentation.

  • Ensure patient confidentiality and safety throughout the study.

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

  • Monitor data quality and clinical trial compliance.

Source Data Verification & CRF Review

  • Conduct Source Document Review (SDR) and Source Data Verification (SDV).

  • Verify accuracy and completeness of CRF/eCRF data.

  • Manage and resolve data queries within timelines.

  • Ensure compliance with Electronic Data Capture (EDC) requirements.

Investigational Product (IP) Management

  • Review IP storage, accountability, and reconciliation records.

  • Verify proper dispensing and administration of investigational products.

  • Ensure compliance with blinding, randomization, and labeling requirements.

Site Management & Documentation

  • Maintain and review Investigator Site Files (ISF).

  • Reconcile ISF with Trial Master File (TMF).

  • Ensure essential documents are archived according to regulations.

  • Prepare monitoring reports, follow-up letters, trip reports, and communication logs.

Site Support & Stakeholder Management

  • Act as primary liaison between study sites and project teams.

  • Support site recruitment, retention, and awareness initiatives.

  • Ensure site staff training and compliance with study requirements.

  • Participate in Investigator Meetings and Sponsor Meetings.

Audit & Inspection Readiness

  • Support audit preparation and inspection readiness activities.

  • Provide guidance on regulatory compliance and quality standards.

  • Assist sites in implementing corrective and preventive actions.

Required Qualifications

Education:

  • Bachelor's Degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or related field

  • Registered Nurse (RN) may also be considered

  • Equivalent combination of education and experience

Experience:

  • Minimum 5+ years of Clinical Monitoring experience.

  • Strong Oncology Clinical Trial experience is mandatory.

  • Experience in site monitoring and management activities.

Required Skills

  • Clinical Research

  • Clinical Trial Monitoring

  • Oncology Studies

  • Site Management

  • ICH-GCP Guidelines

  • Source Data Verification (SDV)

  • Source Document Review (SDR)

  • EDC Systems

  • Investigational Product Management

  • Regulatory Compliance

  • Trial Master File (TMF)

  • Investigator Site File (ISF)

  • Audit Readiness

  • Pharmacovigilance Awareness

  • Stakeholder Management