Site Contracts Associate II

New
Based in IndiaFull-TimeMiddle
Salary not disclosed
Apply NowOpens the employer's application page

Job Details

Languages
English
Experience
2–5 years
Required Skills
Microsoft ExcelPowerPoint

Requirements

  • 2–5 years of experience in site contracting, clinical operations, or a related role within the CRO or life sciences industry.
  • Bachelor’s degree in law, business, economics, social sciences, or a related field, or equivalent professional experience.
  • Strong understanding of clinical trial processes, site agreements, and regulatory requirements such as ICH-GCP.
  • Excellent negotiation, analytical, and contract interpretation skills with strong attention to detail.
  • Ability to manage multiple contracts and priorities in a fast-paced, deadline-driven environment.
  • Strong written and verbal communication skills in English; additional languages are a plus.
  • Proficiency in MS Office tools, particularly Excel, Word, and PowerPoint.
  • Ability to work effectively in a virtual, cross-functional, and global team environment.
  • Strong problem-solving mindset with the ability to identify issues and implement practical solutions.
  • High level of professionalism, organization, and accountability in all deliverables.

Responsibilities

  • Draft, review, and negotiate clinical site agreements and related documents including service agreements, amendments, letters, and notices.
  • Ensure contract terms align with study budgets, negotiation parameters, protocols, timelines, and applicable legal and regulatory requirements such as ICH-GCP.
  • Act as a key liaison between internal teams and clinical sites, ensuring clear communication of contract status, updates, and outstanding issues.
  • Manage the full contract execution process, including coordinating signatures and ensuring timely completion by all stakeholders.
  • Maintain accurate records, tracking systems, and archived documentation in compliance with SOPs and regulatory standards.
  • Identify risks, inconsistencies, or issues in contract terms and collaborate with stakeholders to resolve them effectively.
  • Support site contracting strategy discussions and contribute to process improvements to enhance efficiency and quality.
  • Monitor contracting timelines and milestones, ensuring adherence to agreed delivery schedules and escalation where necessary.
  • Ensure completeness of required documentation such as insurance certificates, indemnification letters, and informed consent-related materials.
View Full Description & ApplyYou'll be redirected to the employer's site
View details
Apply Now