Director, Clinical Science

Recursion•Salt Lake City, UT

4d•$212,900 - $287,980•Remote

About The Position

Recursion is at the forefront of reimagining drug discovery by integrating automated cell biology, high-dimensional and diverse datasets, 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 clinical deliverables (protocols, amendments, medical monitoring plans, annual reports, study-specific updates, CSRs); routine medical monitoring; site interactions/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 in 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.

Requirements

5-7+ years as a Clinical Scientist in a pharmaceutical or biotech company
Prior experience in early phase 1-2 oncology studies is required.
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

Nice To Haves

Experience with hematologic malignancies is preferred.

Responsibilities

Serve as the authoring lead on multiple clinical documents.
Oversee all clinical aspects of a clinical trial(s).
Plan and author clinical deliverables (protocols, amendments, medical monitoring plans, annual reports, study-specific updates, CSRs).
Perform routine medical monitoring.
Handle site interactions/correspondence regarding patient eligibility and treatment inquiries.
Deliver presentations, both internal and external.
Ensure study protocols are executed appropriately and that the study data is both appropriate and pristine.
Review and clean/query pertinent data points.
Identify trends or inconsistencies with the data.
Serve as the face of the study to Investigative Sites.
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.