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Roche

Global pharmaceuticals and diagnostics company

Study Start Up Lead

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeKyiv, UkraineNo salary listed

About the Job

Requirements

  • Have a degree (MD, PhD, MA/MS, BA/BS) in life sciences or a related field.
  • Have at least 4 years of relevant clinical trial operations experience, including clinical trial start-up, regulatory submissions, and cross-functional collaboration.
  • Have a strong understanding of ICH-GCP, EU CTR, and local regulatory environments.
  • Have practical understanding of Ukrainian clinical trial legislation, operations, and regulatory environments, including medicinal products and medical devices.
  • Be fluent in written and spoken English and be a native Ukrainian speaker.
  • Be a resident of Ukraine, able to work in the Roche Ukraine office in Kyiv, and willing to travel.

Responsibilities

  • Lead country strategy for study start-up, driving efficiency, innovation, and collaboration with external stakeholders.
  • Lead start-up operations to ensure timely and efficient site activation and regulatory compliance.
  • Identify and lead opportunities for process automation, standardization, and innovation at country and site levels.
  • Collaborate with local, regional, and global counterparts to harmonize systems and improve timelines.
  • Lead development and management of clinical trial submissions and amendments, ensuring regulatory coordination.
  • Provide strategic oversight and operational delivery of budgeting and contract management, including developing budget strategies and negotiating with internal and external stakeholders.
  • Participate in external industry collaborations to influence the country's start-up environment.
  • Strategically oversee and manage site payment processes, budget escalations, financial reporting, and reconciliation of financial activities.
  • Contribute to local vendor management, excluding CROs, as required to support site activities.
  • Lead development and management of post-trial access submissions and amendments, ensuring strategic planning and execution in accordance with regulatory requirements and local procedures.
  • If acting as a people leader, provide coaching, support, and leadership to a team and help team members develop their skills and careers.

Desired Qualifications

  • A postgraduate degree is highly desirable.

About the Company

Roche

Global pharmaceuticals and diagnostics company

Roche is a global leader in pharmaceuticals and diagnostics. It develops medicines and diagnostic tools that help detect, monitor, and treat diseases, using research and biotechnology to drive new therapies and tests. Roche combines drug development with in-house diagnostic products to support personalized medicine, where treatments are tailored to individual patients based on test results. Its approach differs from many peers by integrating drug discovery with diagnostic capabilities and by expanding its research through strategic acquisitions (like Genentech) to strengthen its biotechnology and R&D capabilities. The company’s goal is to improve patient outcomes and healthcare worldwide by delivering reliable medicines, accurate diagnostic tests, and data-driven care.

Company size
1-10
Company stage
IPO
Headquarters
Basel, Switzerland
Founded
1896

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