Clinical Research Associate (CRA) - Cardiovascular (Remote)

Scorpion Therapeutics; United States; Remote; USD 65,000 - 95,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Research Associate (CRA) responsible for site performance and compliance in a specified country, managing all phases of clinical trial conduct at assigned sites.

You will supervise remote and on-site monitoring, regulatory documentation, and site selection while collaborating with cross-functional teams. Travel (domestic/international) is extensive, and strong English and local language skills are required.

Qualifications

• Requires an Associate's degree or Bachelor's with 5+ years in healthcare/clinical research.
• 2+ years of site management experience in biopharma or CRO.
• Proficiency in GCP, clinical trial processes, and data management.
• Fluent in local language and English; valid driver's license preferred.

Responsibilities

• Conduct remote and on-site monitoring across assigned sites.
• Oversee regulatory documentation and compliance with ICH-GCP.
• Participate in site selection and initiate corrective actions.
• Handle issue resolution and support audits.
• Collaborate with regulatory, pharmacovigilance and legal teams.
• Contribute as a subject matter expert and mentor within the CRA team.

Skills

GCP knowledge

Clinical trial processes

Data management

Site management

English proficiency

Local language proficiency

Driver's license

Education

Associate's degree

Bachelor’s degree

Job description

Role:

Clinical Research Associate (CRA) responsible for site performance and compliance in a specified country, managing all phases of clinical trial conduct at assigned sites.

Objectives:

ensure adherence to ICH-GCP, local regulations, and company policies, while fostering strong site relationships and expanding the research territory.

Responsibilities:

conduct remote and on-site monitoring, oversee regulatory documentation, participate in site selection, handle issue resolution, and support audits; collaborate with cross-functional teams including regulatory, pharmacovigilance, and legal; contribute as subject matter expert and mentor within the CRA team.

Requirements:

Associate's degree or bachelor’s with 5+ years in healthcare/clinical research, including 2+ years of site management experience in biopharma or CRO; proficiency in GCP, clinical trial processes, and data management; fluent in local language and English; valid driver's license preferred.

HighValue:

global trial oversight, site management, 65-75% travel (~2-3 days/week), remote work, experience across phases of clinical trials, strong understanding of GCP/ICH, and regulatory compliance in diverse therapy areas.

Work setup:

remote with extensive domestic and international travel.