Clinical Scientist

Summary

Join Recursion Pharmaceuticals as a contract Clinical Scientist and play a critical role in overseeing all clinical aspects of a Phase I clinical trial. You will be responsible for planning and authoring clinical deliverables, medical monitoring, site interaction, and internal and external presentations. This role involves cross-functional collaboration with various teams, including Clinical Operations, Medical Director, and CROs. You will review and analyze data, identify trends, and serve as the study's point of contact for investigative sites. The position requires managing multiple early-phase projects simultaneously in a fast-paced environment. This remote position offers the potential for on-site visits.

Requirements

• 5+ years as a Clinical Scientist
• Phase 1 oncology experience with hematologic malignancies
• Strong interpersonal and communication skills (both spoken and written) – with ability to effectively communicate on project planning, progress, tracking etc
• Strong relationship building skills to work effectively with others in various disciplines and levels
• Proven ability to manage multiple, complex, and competing priorities to effective and efficient conclusion
• Ability to operate strategically and tactically
• Proven ability in problem solving and issues management that is solution focused

Responsibilities

• Oversee all clinical aspects of a Phase I clinical trial
• Plan and author clinical deliverables (protocols, amendments, and study-specific updates)
• Conduct routine medical monitoring
• Interact with and correspond with sites regarding patient eligibility and treatment inquiries
• Give presentations both internal and external
• Ensure study protocols are executed appropriately and that the study data is both appropriate and pristine
• Interact cross-functionally with multiple disciplines supporting the Study Team (Clinical Operations, Medical Director, CMC, Data Management, CROs, CRAs, Investigative Sites, etc)
• Review and clean / query pertinent data points
• Identify trends or inconsistencies with the data
• Serve as the face of the study to Investigative Sites
• Serve as the authoring lead on clinical documents
• Work with highly dynamic teams where your role will range from leading and owning decisions or timelines to being a key contributor whose experience and insight are relied upon to advance the task at hand
• Be primarily responsible for the quality of your study data
• Review (Medical Monitoring)
• Issue, review, and close queries
• Review TLFs
• Summarize data throughout the trial
• Present the data to management when requested
• Present the protocol procedures and Site Initiation Visits both in-person and virtually
• Support multiple early phase (1-2) studies simultaneously

Preferred Qualifications

• Experience with Bayesian dose escalation designs and/or combination studies
• Authoring experience

Benefits

This is a remote position with the potential for on-site visits for routine work and departmental events