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Worldwide Clinical Trials
Worldwide Clinical Trials
1.001 – 5.000 Angajați
Sponsor pentru viza H1BAsistență medicalăConsultanțăLogistică
Worldwide Clinical Trials este o organizație globală de cercetare clinică pe bază de contract, care sprijină companiile farmaceutice și de biotehnologie pe parcursul întregului ciclu de dezvoltare a medicamentelor. Cu o experiență de peste 30 de ani, compania oferă servicii de monitorizare clinică, gestionare a datelor, recrutare a pacienților și consultanță de reglementare în domenii terapeutice precum oncologia, cardiologia și bolile rare. Abordarea sa combină expertiza vastă în studiile clinice cu sprijin personalizat și soluții adaptate studiilor complexe.
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Locurile de muncă ale companiei

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.

USStatele Unite ale AmericiiNCCarolina de Nord
60.000 $ – 119.000 $ / an
RemoteNormă întreagăJuniorLimbă Obligatorie: englezăGeneralSpecialist contracte
Google Cloud Platform

Descriere

  • 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.

Cerințe

  • 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.

Beneficii

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

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