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Clinical Scientist

  • Full Time, onsite
  • Tundra Technical Solutions
  • Cambridge, United States of America
Salary undisclosed

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  • Contribute to the Systemic Mastocytosis portfolio by collaborating with Medical Directors, pharmacology teams, and external experts.
  • Assist in developing clinical study concepts, writing protocols, and informed consent documents, incorporating feedback from internal and external stakeholders.
  • Participate in the design and execution of clinical studies, ensuring alignment with regulatory requirements and organizational goals.
  • Drive clinical contributions to regulatory queries and submissions, while monitoring safety and efficacy data in ongoing studies to ensure GCP compliance.
  • Attend scientific meetings, engage with investigators, and present data and protocol designs at advisory boards and other relevant forums.