Principal Investigator

Denali Health; Seattle (WA); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

Adaptable scheduling

Supportive infrastructure

Job summary

Denali Health is seeking an experienced physician to serve as Principal Investigator for our clinical research sites. The PI will oversee patient safety, protocol compliance, and the integrity of trials.

This role offers adaptable scheduling (5-10 hours per week) and streamlined operations to support efficient study execution. We seek a board-certified clinician with at least 2 years as PI or Sub-Investigator.

Qualifications

• MD or DO degree required; PhD may be considered.
• Board certification in a relevant medical specialty preferred.
• Minimum of 2 years of experience as a Principal Investigator or Sub-Investigator in clinical trials.

Responsibilities

• Regulatory documentation: Review and sign essential regulatory documents.
• During and post-study responsibilities: Oversee patient safety and required clinical assessments.
• Study conduct & subject management: Provide medical oversight; our team manages daily operations.
• Safety reporting & documentation: Assess adverse events with full documentation support.

Education

MD or DO degree

PhD may be considered

Board certification in a relevant medical specialty preferred

Job description

Denali Health is seeking an experienced Physician to serve as Principal Investigator (PI) for our dedicated clinical research sites. The PI will be responsible for ensuring the integrity and patient safety of the clinical trials. The ideal Principal Investigator will have a strong background in clinical research, a commitment to upholding the highest ethical standards, and a passion for advancing medical science.

Key Benefits of the Opportunity

Adaptable Scheduling

Commitment typically requires 5-10 hours per week

Streamlined Operations

Denali's world-class operations, regulatory, compliance, and clinical services infrastructure to make being an investigator as smooth as possible.

Key Responsibilities

Regulatory Documentation

Review and sign essential regulatory documents

During/Post Study Responsibilities

Oversee patient safety and required clinical assessments.

Study Conduct & Subject Management

Provide medical oversight; our team manages daily operations.

Safety Reporting & Documentation

Assess adverse events with full documentation support.

Qualifications

Education

• MD or DO degree required. A PhD, in a related field may be considered.
• Board certification in a relevant medical specialty is preferred

Experience

• Minimum of 2 years of experience as a Principal Investigator or Sub-Investigator in clinical trials.

Why Denali Health?

At Denali Health, we are committed to accelerating therapeutic innovations by breaking the bottlenecks in research and bridging the gap from bench to market. Denali Health promotes an inclusive environment that fosters independence & career growth. Join our team and be part of a dynamic organization that values integrity, innovation, and excellence in clinical research.

Denali Health is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.