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Site Start Up Euctr Ii

Parexel
3-4 years
INR 8 LPA – 14 LPA
Hyderabad
1 June 24, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

SITE START UP EUCTR II

Company: Parexel
Location: Hyderabad, India
Job ID: R0000042680
Category: Clinical Trials
Job Type: Full-Time

JOB OVERVIEW

Parexel is seeking a Site Start Up EUCTR II professional responsible for planning, coordinating, and submitting complex European Clinical Trial Regulation (EUCTR/CTIS) submissions for large Phase II and Phase III clinical trials involving multiple countries and sites. The role requires expertise in study start-up activities, regulatory submissions, stakeholder coordination, and compliance with European clinical trial regulations.

KEY RESPONSIBILITIES

• EUCTR / CTIS Submission Management

  • Plan and manage complex EUCTR submissions.

  • Support large multinational Phase II and Phase III clinical trials.

  • Coordinate submissions across multiple countries and clinical sites.

  • Ensure timely regulatory approvals and submissions.

• Clinical Study Start-Up

  • Support end-to-end study start-up activities.

  • Coordinate with cross-functional teams during study initiation.

  • Monitor submission timelines and milestones.

  • Ensure study start-up deliverables are completed on schedule.

• Regulatory Compliance

  • Ensure compliance with:

    • EU Clinical Trial Regulation (EUCTR/CTIS)

    • ICH Guidelines

    • Good Clinical Practice (GCP)

    • IVDR Regulatory Requirements

  • Maintain high-quality regulatory documentation.

• Stakeholder & Vendor Management

  • Collaborate with sponsors, regulatory teams, and study teams.

  • Coordinate activities with external vendors.

  • Build productive working relationships across project teams.

  • Resolve operational and regulatory issues proactively.

• Trial Management Support

  • Utilize Clinical Trial Management Systems (CTMS).

  • Support Trial Master File (TMF) maintenance.

  • Track study progress and submission status.

  • Provide updates and reports to stakeholders.

• Project Planning & Execution

  • Apply data-driven approaches to planning and execution.

  • Identify risks and implement mitigation strategies.

  • Manage competing priorities and deadlines.

  • Support operational strategy implementation.

REQUIRED QUALIFICATIONS

  • Bachelor’s Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Clinical Research

    • Related Scientific Discipline

EXPERIENCE

3–4 Years

Experience in:

  • Clinical Trial Start-Up

  • Regulatory Submissions

  • EUCTR / CTIS Submissions

  • Clinical Operations

  • CRO Industry

  • Multinational Clinical Trials