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Site Specialist - Contracts & Budgets

Icon Plc
ICON PLC
3+ years
Not Disclosed
Chennai, India
10 March 18, 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 – Contracts & Budgets (Clinical Trial Agreements & Site Activation)

Location: Chennai, India
Job Type: Full-Time | Office with Flex
Company: ICON plc
Job ID: JR145157

About the Role
ICON plc, a global leader in healthcare intelligence and clinical research, is hiring a Site Specialist – Contracts & Budgets to join its high-performing Site Activation team. This role focuses on managing clinical trial agreements (CTAs), site budgets, and contract execution to ensure efficient and compliant study start-up across global trials.

Key Responsibilities

  • Lead negotiation, execution, and management of Clinical Trial Agreements (CTAs) and site budgets with investigative sites

  • Collaborate with Clinical Operations and Project Management teams to ensure timely site activation

  • Track and forecast contract timelines to support study start-up planning

  • Ensure compliance with local regulations, legal requirements, and SOPs

  • Support regulatory submissions including EC/IRB documentation

  • Review contract changes, assess risks, and escalate deviations when required

  • Manage multiple contracts simultaneously in a fast-paced environment

  • Maintain accurate documentation and contract records

  • Identify and escalate risks or issues to stakeholders

  • Mentor junior team members and support team development

  • Contribute to process improvements and operational efficiency

Required Qualifications & Experience

  • Bachelor’s degree in Life Sciences or related field (or equivalent experience)

  • Minimum 3+ years of experience in clinical trial contracts and budget negotiation

  • Strong understanding of clinical trial regulations and compliance requirements

  • Experience in CTA negotiation, site budgeting, and study start-up

  • Ability to manage multiple priorities and meet deadlines

  • Strong analytical, negotiation, and problem-solving skills

  • Excellent communication and stakeholder management abilities

  • High attention to detail and risk assessment skills

Preferred Skills

  • Experience in global clinical trials

  • Familiarity with contract management systems

  • Understanding of legal and financial terms in clinical agreements

Why Join ICON
ICON offers a collaborative and innovation-driven environment focused on clinical excellence and operational efficiency.

Key Benefits Include

  • Competitive salary and career growth opportunities

  • Flexible work environment

  • Generous leave policies

  • Health insurance coverage

  • Retirement and financial planning benefits

  • Employee Assistance Programme

  • Life insurance and wellness programs

  • Additional country-specific benefits

Diversity, Equity & Inclusion
ICON is committed to an inclusive workplace where all qualified applicants receive equal opportunity.

Application Note
Candidates are encouraged to apply even if they do not meet all requirements. ICON supports continuous learning and career development.