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Worldwide Clinical Trials

Contract research organization delivering clinical trials

Site Contracts Specialist - Site Contracts

Contract ManagementPosted on Nov 12
Full-timeNo salary listed

About the Job

Requirements

  • A bachelor’s degree or equivalent in business administration, finance, science, or a related field is required.
  • One to three years of experience in the clinical research, pharmaceutical, or contract research organization industry working with investigator/site contracts or in a related legal field is required.
  • Excellent verbal and written proficiency in English is required.
  • Experience negotiating clinical site contracts and budgets, including the ability to identify contractual risks, discrepancies, and potential issues, is required.
  • Knowledge and understanding of ICH-GCP guidelines, clinical trial regulations, and applicable local regulatory requirements are required.
  • Strong communication, analytical, problem-solving, project management, and organizational skills, including the ability to manage multiple contracts and deadlines, are required.
  • Proficiency in Microsoft Word, Excel, Outlook, and contract management tools is required.
  • An understanding of budgeting, financial principles, and legal terminology related to clinical trial contracts is required.

Responsibilities

  • Prepare, draft, negotiate, and finalize site agreements, amendments, budgets, and other site-related contractual documents.
  • Negotiate contract language and study budgets with assigned clinical research sites through execution.
  • Review agreements and supporting documents for completeness, accuracy, quality, and compliance before signature.
  • Identify and escalate contractual risks, requests outside approved parameters, and non-responsive sites to the appropriate study stakeholders.
  • Collaborate with Legal, Data Privacy, study teams, sponsors, sites, and investigators to resolve contract-related questions and issues.
  • Facilitate contract execution and distribute fully executed agreements to relevant teams and stakeholders.
  • Maintain accurate, real-time tracking of contracting activities, negotiation status, timelines, and deliverables.
  • Support additional contracting activities, including amendments, termination letters, donation agreements, translations, and regulatory submission documentation as applicable.
  • Prioritize multiple site contracts and respond effectively to urgent requests from internal teams and sponsors.

About the Company

Worldwide Clinical Trials

Contract research organization delivering clinical trials

Worldwide Clinical Trials is a contract research organization that provides drug development services for pharmaceutical and biotech companies, focusing on running clinical trials to bring new medicines to market. Its core work centers on the science and logistics of clinical trials—designing studies, coordinating sites and investigators, and managing data and regulatory processes to advance drug candidates through development. The company differentiates itself through its specialized, science-driven approach and global expansion achieved via strategic acquisitions, building a larger network and broader capabilities to support complex trial programs. After a history of ownership changes, including a re-launch in 2007 and a majority stake sale in 2023, the firm aims to grow further under new ownership while continuing to offer focused clinical trial services that support medical advancement.

Company size
1,001-5,000
Company stage
Acquired
Total funding
Not listed
Headquarters
Morrisville, NC
Founded
1986

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