Clinical Research Lead - Oncology Trials & Coordination

Proclinical Group

Basel

Vor Ort

CHF 90.000 - 140.000

Vollzeit

14 Tage+
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Zusammenfassung

Proclinical Group in Basel seeks a Clinical Research Scientist/Coordinator to contribute to the design, execution, and oversight of global clinical studies, focusing on low-complexity trials. You will collaborate with cross-functional teams to meet study deliverables while upholding high scientific and operational standards.

The ideal candidate has a strong background in clinical research, especially in oncology or hematology, and demonstrates leadership, problem-solving, and familiarity with

Qualifikationen

  • Experience leading clinical studies and multi-site coordination.
  • Strong understanding of regulatory and ICH-GCP guidelines.
  • Background in oncology or hematology is highly desirable.
  • Ability to manage multiple studies and strict timelines.
  • Excellent communication and collaboration skills.

Aufgaben

  • Lead or support development of clinical protocols, amendments, and related study documents in collaboration with the Medical Lead and other teams.
  • Provide medical and scientific input for study-related processes and regulatory documents.
  • Contribute to study concept feasibility assessments and operational execution plans.
  • Collaborate with cross-functional teams to identify and select high-performing sites to meet recruitment goals.
  • Lead or support global cross-functional Clinical Trial Teams (CTTs) to ensure timely delivery of trial objectives.
  • Conduct ongoing medical-scientific reviews of clinical trial data, including safety trend analysis, signal detection, and data interpretation.
  • Prepare and lead dose escalation meetings and coordinate real-time availability of quality clinical trial data.
  • Proactively manage risk mitigation and implementation strategies at the trial level.
  • Forecast and manage study budgets in collaboration with relevant stakeholders.
  • Set vendor strategies and timelines for assigned studies.
  • Implement best practices and standards for trial management, sharing lessons learned across teams.
  • Represent the group in cross-functional initiatives and act as a Subject Matter Expert when required.

Kenntnisse

Clinical trial management
Leadership
Regulatory knowledge
Study coordination
Medical input

Ausbildung

Master's degree in life sciences
PhD/MD preferred

Jobbeschreibung

Proclinical Group in Basel seeks a Clinical Research Scientist/Coordinator to contribute to the design, execution, and oversight of global clinical studies, focusing on low-complexity trials. You will collaborate with cross-functional teams to meet study deliverables while upholding high scientific and operational standards.

The ideal candidate has a strong background in clinical research, especially in oncology or hematology, and demonstrates leadership, problem-solving, and familiarity with

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