Recursion Pharmaceuticals
Director, Clinical Science
New York, New York; Salt Lake City, Utah · Director
Sponsorship not specified$234k-$288kDetected 5 days ago
RecruitingLeadershipCommunicationCollaborationProblem SolvingTime ManagementPublic Speaking
About the role
- The Impact You'll Make Recursion is at the forefront of reimagining drug discovery by integrating automated cell biology, high-dimensional and diverse datasets, and sophisticated analytics.
- 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).
Responsibilities
- 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
- We take ownership and accountability. Through ownership and accountability, we enable trust and autonomy-leaders take accountability for decisive action, and teams own outcomes together.
- Travel may be necessary from time to time to support collaboration, team events, meetings, or other business needs.
- They are the character and personality of the company demonstrated through how we communicate, support one another, spend our time, make decisions, and celebrate collectively.
- Powered by proprietary multimodal data, purpose-built AI models, and bilingual teams fluent in both science and AI, the Recursion OS is designed to translate complex science into medicines that matter - faster, better, and at scale - for patients who are waiting.
- Recursion also maintains offices in New York, Montréal, and London, three global hubs for talent and leadership at the intersection of AI and scientific innovation.
- Create - Serve as the authoring lead on multiple clinical documents.
- While this will not refer to manuals, it does encompass Clinical documents and site/agency interactions.
- Drive & Deliver - You will be primarily responsible for the quality of your study data.
Requirements
- 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.
- You will also be required to present the protocol procedures and Site Initiation Visits both in-person and virtually.
Nice to have
- Experience with hematologic malignancies is preferred.
Compensation
- Based on the skills, experience, and qualifications needed for this role, the estimated annual base salary range is:
- New York City, Boston, & San Francisco Bay Area(s): $234,190-$287,980
- Salt Lake City & all other U.S. locations: $212,900-$261,800
- In addition to base salary, this role is eligible for an annual bonus, equity compensation, and a comprehensive benefits package.
Benefits
- Recursion is moving away from the use of Medical Writers and relying more heavily on the Clinical Scientist and Medical Director to author IND and study-specific documents.
- This will include reviewing (Medical Monitoring); issuing, reviewing, and closing queries; reviewing TLFs, summarizing data throughout the trial, and presenting the data to management when requested.
Company info
- Reporting to the Vice President, Clinical Science, you'll be joining the Clinical Science Team within Clinical Development.
- This group is ultimately responsible for shepherding an experimental drug from IND through Dose Finding, Proof of Concept, and possibly Registration studies.
- Clinical Science consists of a high-performing team of extremely motivated individuals who work independently, interact cross-functionally with many contributing departments, and are capable of multitasking to expeditiously execute cutting-edge clinical trials.
- The Experience You'll Need
- 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.
- Ability to operate strategically and tactically
- Proven ability in problem-solving and issues management that is solution-focused
- Working Location & Compensation:
- This is a fully remote opportunity with occasional travel requirements.
Equal opportunity
- Recursion is an Equal Opportunity Employer.
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