Clinical Scientist

Edgewise Therapeutics, Inc.; New York (NY); On-site; USD 135,000 - 175,000; Full time

Job summary

Edgewise Therapeutics, Inc. seeks a Clinical Scientist to support late-stage clinical development of muscle-targeted cardiovascular therapeutics.

The role involves maintaining disease area expertise, collaborating across functional teams, conducting clinical data review, and contributing to drug development strategy and regulatory documentation. Responsibilities include representing clinical science perspectives in sub-teams, delivering presentations, and staying current on therapeutic

Qualifications

• PhD in relevant field; cardiovascular expertise highly desired.
• 5+ years of late-stage clinical development experience.
• Strong interpersonal skills to lead study teams and provide medical guidance.
• Proactive problem-solving and negotiation capabilities.
• Excellent communication skills for cross-functional collaboration.

Responsibilities

• Represent clinical science perspectives in sub-teams and deliver presentations.
• Maintain current knowledge of therapeutic area developments and competitive landscape.
• Contribute to clinical trial strategy, protocols, and regulatory documents.
• Review study data, identify trends and protocol deviations, and elevate safety events.
• Collaborate with clinical operations on investigator meetings and study materials.

Skills

Interpersonal skills

Cross-functional collaboration

Problem-solving

Negotiation

Communication skills

Education

PhD in relevant field (Cardiovascular)

Job description

Edgewise Therapeutics seeks a Clinical Scientist to support late-stage clinical development of muscle-targeted cardiovascular therapeutics. The role involves maintaining disease area expertise, collaborating across functional teams, conducting clinical data review, and contributing to drug development strategy and regulatory documentation.

Responsibilities

Represent clinical science perspectives in sub-teams and deliver presentationsMaintain current knowledge of therapeutic area developments and competitive landscapeContribute to clinical trial strategy, protocols, and regulatory documentsReview study data, identify trends and protocol deviations, and elevate safety eventsCollaborate with clinical operations on investigator meetings and study materials

Requirements

PhD in relevant field; cardiovascular expertise highly desired5+ years late-stage clinical development experienceStrong interpersonal skills to lead study teams and provide medical guidanceProactive problem-solving and negotiation capabilitiesExcellent communication skills for cross-functional collaboration

Compensation

$135,000-$175,000, commensurate with experience