Faro Health aims to improve lives by helping life sciences companies answer complex clinical questions, simply, efficiently and effectively. Our software platform is used to orchestrate complex clinical development with a single source of truth. It brings words, data and teams together, empowering researchers to design more intelligent trials, master complexity and reach milestones faster.

The Clinical Strategy and Solutions Specialist - Study Modeling will support all aspects of study modeling within the Faro Study Designer to ensure quality of studies modeled supporting the success of our users and supports the enhancement of data-driven features on the Faro Health Platform. In this role, you will utilize your expertise in Clinical Operations to understand and reflect clinical protocols in the Faro Health Platform across a variety of Therapeutic Areas and Study Designs.

This position is remote and offers flexible work hours. Open to candidates who currently reside in California, Nevada, Wisconsin, North Carolina, Pennsylvania, Virginia or New York only.

Requirements

Duties and 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.

Qualifications

• 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 
• Oncology experience a plus
• 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

Skills and Competencies

• Strong organizational, motivational, and leadership skills, promoting a team-based approach
• Strong attention to detail skills and ability to triage and aid in resolution of escalations
• Ability to work independently or in a group setting; ability to adjust to changing priorities
• Strong emotional intelligence, interpersonal and communication skills, both verbal and written
• Strong organizational and leadership skills
• Strong problem solving skills
• Goal-oriented
• Ability to project and maintain a professional and positive attitude
• Strong ability to learn and utilize technology to execute job responsibilities  

Benefits

Salary

• Hourly range for this position is $50 to $100 per hour
• This is a 3 month contract with possibility for extension and must be able to work 20-40 hours per week.
• Individual hourly pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training.
• Open to candidates who currently reside in California, Nevada, Wisconsin, North Carolina, Pennsylvania, Virginia and New York only.