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Site Specialist

Icon
ICON
3+ years
preferred by company
10 Jan. 15, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Site Specialist II – Study Start-Up (Clinical Research)

Locations: Bangalore | Chennai | Bengaluru, India
Job ID: JR140853
Employment Type: Full-Time
Work Model: Office-Based with Flexibility
Business Unit: ICON Full Service & Corporate Support
Function: Study Start-Up / Site Activation

About ICON plc

ICON plc is a world-leading healthcare intelligence and clinical research organization committed to advancing clinical development through innovation, quality, and collaboration. With a strong global presence, ICON fosters an inclusive culture where professionals are empowered to deliver excellence across clinical trials worldwide.

Role Overview

ICON is seeking a Site Specialist II to join its high-performing Site Activation (Study Start-Up) team in India. This role is critical to the successful start-up, maintenance, and contract management of clinical trial sites. The position offers hands-on involvement in essential site-level activities that ensure timely, compliant, and efficient site activation across global clinical programs.

Key Responsibilities

  • Support study start-up activities, including essential document review, site readiness checks, and green light process coordination.

  • Manage site maintenance activities, including site-specific Informed Consent Form (ICF) customization, translation coordination, and EC/IRB submissions.

  • Maintain accurate and compliant documentation within eTMF systems in alignment with regulatory requirements.

  • Assist with site contract management, including understanding contract workflows, managing amendments, supporting negotiations, and tracking executed agreements.

  • Collaborate with cross-functional internal teams and external stakeholders to meet study timelines and quality standards.

  • Communicate effectively with global teams using strong written and verbal communication skills.

  • Work flexible hours as required to support international clinical trial operations.

Required Qualifications & Experience

  • Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, Business Administration, or a related discipline.

  • Minimum 3+ years of relevant experience in clinical trial study start-up, site activation, maintenance activities, and site contract management.

  • Strong knowledge of ICF processes, IRB/EC submissions, translation workflows, and clinical trial documentation.

  • Exposure to site contract negotiations and amendments is highly desirable.

  • Excellent organizational and multitasking skills with strong attention to detail.

  • Ability to work independently and collaboratively in a global, matrix environment.

  • Willingness to work flexible shifts aligned with global project needs.

What ICON Offers

  • Competitive salary aligned with industry benchmarks.

  • Comprehensive health insurance coverage for employees and dependents.

  • Retirement and long-term financial planning benefits.

  • Global Employee Assistance Program (LifeWorks) with 24/7 access to professional well-being support.

  • Life assurance coverage.

  • Flexible, country-specific benefits including wellness programs, childcare support, gym memberships, travel subsidies, and more.

  • An inclusive, performance-driven culture that supports career growth and work-life balance.

Diversity, Equity & Inclusion

ICON is committed to fostering a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration for employment regardless of race, color, religion, gender, sexual orientation, gender identity, nationality, disability, or veteran status.

Accessibility & Accommodations

Reasonable accommodations are available for candidates with medical conditions or disabilities throughout the recruitment and employment process.

Why Join ICON?

Candidates who may not meet every requirement are still encouraged to apply. ICON values potential, diversity, and passion for clinical research, and this role may lead to future opportunities within ICON’s global organization.a