Worldwide Clinical Trials
Worldwide Clinical Trials
Worldwide Clinical Trials एक वैश्विक कॉन्ट्रैक्ट रिसर्च ऑर्गनाइज़ेशन है, जो दवा विकास के पूरे जीवनचक्र में फार्मास्युटिकल और बायोटेक्नोलॉजी कंपनियों को सहयोग प्रदान करता है। 30 से अधिक वर्षों के अनुभव के साथ, कंपनी ऑन्कोलॉजी, कार्डियोलॉजी और दुर्लभ रोगों सहित विभिन्न उपचार क्षेत्रों में क्लिनिकल मॉनिटरिंग, डेटा प्रबंधन, मरीजों की भर्ती और नियामकीय परामर्श सेवाएँ देती है। इसका दृष्टिकोण व्यापक क्लिनिकल ट्रायल विशेषज्ञता को जटिल अध्ययनों के लिए व्यक्तिगत सहयोग और अनुरूप समाधानों के साथ जोड़ता है।

Site Contracts Specialist - North Carolina Remote

Manage the negotiation and execution of clinical trial agreements for Worldwide Clinical Trials, a global contract research organization. Coordinate budgets, compliance, risk management, and study-startup timelines with sponsors and clinical sites.

विवरण

  • Develop and tailor country-specific contract templates and site agreement documents for clinical trial startup.
  • Negotiate site contract language, budgets, amendments, and related agreements through completion.
  • Assess contract provisions, study budgets, and related costs for accuracy, compliance, and consistency with approved parameters.
  • Collaborate with sponsors, clinical sites, legal, data privacy, regulatory, and study teams to resolve issues and progress negotiations.
  • Recognize and escalate contractual risks, budget issues, and site-related obstacles.
  • Perform quality checks on contracts and supporting documentation before signature and final execution.
  • Coordinate agreement execution and share completed contracts with the appropriate stakeholders and systems.
  • Keep contract tracking systems current and report on negotiation progress, deadlines, and deliverables.
  • Manage competing priorities and urgent requests while contributing to study-startup goals.

आवश्यकताएँ

  • Bachelor’s degree or equivalent qualification in business administration, finance, science, or a related discipline.
  • One to three years of experience in clinical research, pharmaceuticals, contract research organizations, investigator or site contracts, or a related legal field.
  • Fluent English communication skills, both written and verbal.
  • Working knowledge of ICH-GCP guidelines, clinical trial regulations, and applicable local regulatory requirements.
  • Experience negotiating contract terms, budgets, amendments, and related agreements with clinical research sites.
  • Strong analytical and problem-solving capabilities, including risk identification, issue resolution, and interpretation of contractual and financial information.
  • Proficiency with Microsoft Word, Excel, and Outlook.
  • Experience working with contract management systems and related tools.
  • Ability to balance multiple priorities, collaborate across functions, and maintain accuracy and close attention to detail.

लाभ

  • Location-dependent competitive benefits package.
  • Transparent compensation practices and commitment to pay equity.
  • Inclusive and equitable workplace.

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