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Sr Clinical Trial Coordinator / Clinical Trial Coordinator Ii

4+ years
Not Disclosed
10 Nov. 14, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Sr Clinical Trial Coordinator / Clinical Trial Coordinator II

Job ID: R-01329124
Location: Remote, India
Job Type: Full-time
Category: Clinical Research
Work Mode: Fully Remote
Work Schedule: Second Shift (Afternoons)
Environment: Office (remote setup)


Job Overview

The Clinical Trial Coordinator (CTC) / Project Specialist is a core member of the Global Study Team responsible for ensuring a clinical study is delivered on time, within budget, and in full compliance with quality and inspection-readiness standards. The role plays a key part in eTMF completeness, cross-functional coordination, and continuous operational improvement.


Key Responsibilities

1. Study Operations & Oversight

  • Support the Study Manager/Study Delivery Lead (SDL) in end-to-end study operations from start-up to archival.

  • Set up, update, and maintain:

    • Internal systems

    • Databases

    • Tracking tools

    • Project plans (CSAP)

2. Cross-Functional Collaboration

  • Work with internal and external partners to ensure smooth clinical study execution across all phases and therapeutic areas.

  • Follow STOM guidelines, study regulations, SOPs, and industry best practices.

3. Study Monitoring & Risk Management

  • Track study progress and conduct.

  • Identify, resolve, and escalate issues related to timelines, quality, or budget.

  • Maintain oversight of country-specific activities:

    • Recruitment

    • Data completeness

    • Local budgets

    • Protocol deviations

    • Regulatory approvals

    • Import license status

4. Documentation & Study Plans

  • Review clinical documents such as:

    • Protocol

    • Informed Consent Forms (ICFs)

  • Lead preparation of study-specific plans including:

    • Monitoring Plan

    • Vendor Management Plan

    • Protocol Deviation Plan

    • Risk Management Plan

    • Communication Plan

5. Vendor Management & CRO Oversight

  • Act as the primary point of contact for CROs and third-party vendors.

  • Oversee deliverables, monitor performance, and ensure timely completion of delegated activities.

6. Communication & Coordination

  • Organize and manage study meetings:

    • Schedule

    • Prepare materials

    • Write meeting minutes

  • Maintain team information spaces, newsletters, action logs, and communication plans.

7. Clinical Supplies Oversight

  • Track delivery and continuity of study supplies, investigational products, and sponsor-provided materials.

  • Identify supply risks and propose mitigation measures.

8. Data Quality & eTMF Management

  • Ensure inspection readiness at all times.

  • Oversee eTMF setup, quality review, completeness checks, and follow-up on missing documents.

  • Manage Safety Report Dissemination.

9. Budget Tracking

  • Manage task orders, change orders, expenses, and tracking updates.

  • Verify consistency between systems and agreements.

  • Escalate financial issues to the SDL.


Education Requirements

  • Bachelor’s degree in Life Sciences or related field.


Experience Requirements

  • 4+ years of experience in a pharmaceutical/scientific environment.

  • Strong knowledge of:

    • Clinical trials

    • ICH-GCP guidelines

    • Drug development processes

    • Clinical trial systems (including Trial Master File standards)

  • Experience in project management and financial tracking.


Skills & Competencies

Technical Skills

  • Strong understanding of clinical trial regulatory requirements (GCP, ICH).

  • Proficiency in Microsoft Office (especially advanced Excel).

  • Skilled in clinical systems and eTMF tools.

Soft Skills

  • Excellent written and verbal communication.

  • Strong planning, organization, and time-management skills.

  • Analytical, logical, detail-oriented mindset.

  • Ability to handle multiple priorities.

  • Strong interpersonal and stakeholder management skills.

  • Culturally adaptable and collaborative.


What We Offer

  • Opportunity to contribute to groundbreaking therapies.

  • Comprehensive training & professional development.

  • Supportive, collaborative work culture.

  • Competitive compensation and benefits.


Working Conditions

  • Work performed in a remote office setting.

  • Occasional travel to study sites may be required.

  • Exposure to standard office equipment.