Clinical Strategy And Solutions Specialist - Study Modeling

Summary

Join Faro Health as a Clinical Strategy and Solutions Specialist - Study Modeling and contribute to improving lives by helping life sciences companies answer complex clinical questions. You will support all aspects of study modeling within the Faro Study Designer, ensuring quality and success for our users. This remote position offers flexible work hours and requires expertise in Clinical Operations to understand and reflect clinical protocols in the Faro Health Platform. The role involves modeling studies, conducting quality control, assisting in developing standardized documents, and working 20-40 hours per week. This is a 3-month contract with the possibility of extension. Open to candidates residing in specific states only.

Requirements

• Bachelor’s degree required, preferably in physical or life science or statistics discipline
• 5+ years of Clinical Operations work experience in pharmaceutical clinical trials
• Experience as a Clinical Research Associate
• Strong knowledge of clinical trials and drug development processes
• Ability to read and comprehend complex clinical trial protocols and designs
• Familiarity with and experience using clinical trial technologies (e.g., EDC, IRT, CTMS, ePRO, eCOA, eConsent, TMF)
• Knowledge of regulatory requirements and information governance frameworks (e.g. ICH, GCP, HIPAA, GDPR)
• Excellent team player with demonstrated track record of success in a cross-functional team environment; consistent commitment to delivering on team goals with a sense of shared urgency

Responsibilities

• Conduct modeling of publicly available studies in the Faro Study Designer for customers, sales demos and continuous buildout of the public study library. Modeling includes review of protocol documents and building of study designs in the Faro Study Designer. Thorough comprehension of protocol content is critical
• Conduct clinical QC of public study library modeled studies
• Conduct QC of Clinical Data Management gap assessments of public studies for customer, sales demo, and public study library modeled studies
• Assist and support the development and maintenance of a library of standardized clinical trial documents/templates, language templates, workshop materials, documentation, and procedures
• Ability to work 20-40 hours per week

Preferred Qualifications

Oncology experience a plus

Benefits

• This position is remote and offers flexible work hours
• Hourly range for this position is $50 to $100 per hour
• This is a 3 month contract with possibility for extension