WhatsApp Group
Join Now
WhatsApp Channel
Join Now
Telegram Group
Join Now

Clinical Research Site Activation Careers – Apply for Site Specialist at Icon Plc

Published on

ICON plc

1 - 3 Years

Bangalore & Chennai (Remote / Onsite)

B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences

Verified Job

Online Application

Why Use Pharmabharat?

Real-Time Job Alerts

Trusted by Top Pharma Employers

Exclusive Pharma Industry Insights

Verified & Trusted Listings

Are you looking for clinical research jobs in Bangalore or ChennaiICON plc, a global leader in healthcare intelligence and clinical research, is hiring a Site Specialist II to join their Site Activation team. This is an excellent opportunity for professionals with experience in study start-up, site maintenance, and contract management in clinical trials.

Job Title: Site Specialist II

Location: Bangalore / Chennai (Office with Flex)
Job Type: Full-time
Posted: Recently
Requisition ID: JR129390

Job Description

Key Responsibilities:

As a Site Specialist II at ICON plc, you will play a crucial role in ensuring the smooth activation and maintenance of clinical trial sites. Your responsibilities will include:

  • Study Start-Up Activities:
    • Reviewing essential documents for site activation.
    • Managing the green light process to ensure sites are ready for initiation.
    • Coordinating with cross-functional teams to meet study timelines.
  • Site Maintenance Tasks:
    • Customizing site-specific Informed Consent Forms (ICFs).
    • Managing translation workflows for study documents.
    • Handling Ethics Committee (EC) & Institutional Review Board (IRB) submissions.
    • Ensuring proper documentation in eTMF (electronic Trial Master File) systems.
  • Contract Management:
    • Assisting in site contract negotiations and amendments.
    • Ensuring timely finalization of executed agreements.
    • Collaborating with legal and finance teams for contract compliance.
  • Global Collaboration:
    • Working with international teams to support clinical trial operations.
    • Maintaining clear communication with internal and external stakeholders.

Qualifications & Skills Required:

  • Bachelor’s degree in Life Sciences, Business, or related field.
  • Experience in clinical research site activation, maintenance, or contract management.
  • Strong understanding of ICF customization, IRB/EC submissions, and contract workflows.
  • Excellent organizational and multitasking abilities.
  • Strong written and verbal communication skills.
  • Willingness to work flexible hours to support global operations.

Why Join ICON plc?

ICON plc is a top employer in clinical research, offering a supportive and inclusive work environment. Employees enjoy:

  • Competitive salary & benefits (health insurance, retirement plans).
  • Flexible work options (Office with Flex).
  • Global Employee Assistance Programme (24/7 support).
  • Career growth opportunities in a leading CRO.

How to Apply?

Application Link

Clinical Research Site Activation Careers - Apply for Site Specialist at Icon Plc