Recursion Pharmaceuticals-posted 3 months ago
$180,600 - $229,000/Yr
Full-time • Senior
Hybrid • New York, NY
501-1,000 employees
Chemical Manufacturing

Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking a Director level Clinical Scientist who can oversee all clinical aspects of a clinical trial(s). This would include: planning and authoring of clinical deliverables (protocols, amendments, medical monitoring plans, annual reports, study-specific updates, CSRs), routine medical monitoring, site interaction / correspondence re: patient eligibility and treatment inquiries, and presentations both internal and external. As an Associate Director within Clinical Science, you'll play a critical role ensuring study protocols are executed appropriately and that the study data is both appropriate and pristine. On a daily basis, you will interact cross-functionally with multiple disciplines supporting the Study Team (Clinical Operations, Medical Director, CMC, Data Management, CROs, CRAs, Investigative Sites, etc). You'll be responsible for reviewing and cleaning / querying pertinent data points, identifying trends or inconsistencies with the data, and serving as the face of the study to Investigative Sites. You can expect to work on multiple early-phase projects at the same time in a fast-paced and exciting environment where the ability to multi-task and rapidly re-organize thoughts and priorities will be essential.

  • Serve as the authoring lead on multiple clinical documents.
  • Work with highly dynamic teams where your role will range from leading and owning decisions or timelines to being a key contributor.
  • Review and clean/query pertinent data points, identifying trends or inconsistencies with the data.
  • 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.
  • 5+ years as a Clinical Scientist in a pharmaceutical or biotech company.
  • Prior experience in early phase 1-2 oncology studies is required.
  • Experience with hematologic malignancies is preferred.
  • Strong interpersonal and communication skills (both spoken and written).
  • Strong relationship building skills to work effectively with others in various disciplines and levels.
  • Proven ability to manage multiple, complex, and competing priorities.
  • Ability to operate strategically and tactically.
  • Proven ability in problem solving and issues management that is solution focused.
  • Annual bonus and equity compensation.
  • Comprehensive benefits package.
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