Clinical Strategy and Solutions Manager (Temp 12 Months)

Faro Health aims to improve lives by helping life sciences companies answer complex clinical questions simply, efficiently, and effectively. Our platform brings words, data, and teams together to support intelligent clinical trial design. This role supports Faro’s AI systems by producing high quality structured data through data entry and data labeling.

Role Overview

The Clinical Data Entry and Labeling Associate is an internal, part time role focused on structured data production for AI quality assessment and improvement. The role combines data entry and data labeling work performed using predefined rules and guidelines. The emphasis is on accuracy, consistency, and throughput rather than independent clinical judgment or customer interaction.

Duties and Responsibilities

• Extract information from clinical trial protocols and related documents and enter it into structured fields in the Faro platform
• Apply labeling and annotation guidelines to structured data to support AI model training and evaluation
• Follow defined rules and quality standards consistently across large volumes of work
• Perform self review and peer review using established quality check processes
• Flag ambiguous or unclear source content for review rather than resolving independently
• Meet accuracy and productivity expectations for data entry and data labeling tasks
• Collaborate cross‑functionally to capture recurring issues, translate them into actionable product/training improvements

**NOTE: Candidates and Recruiting Agencies, please do not contact our employees regarding the position or your application status. Doing so will automatically disqualify you from the position or working with us. Only applications submitted through the designated link will be considered. Please DO NOT SPAM our employees regarding the role or your application status.

Requirements

Qualifications

• Bachelor’s degree required, preferably in physical or life science or statistics discipline
• 5-7+ years of Clinical Operations work experience at a sponsor company in pharmaceutical clinical trials preferred. Experience as a Clinical Research Associate a plus. 
• Strong knowledge of clinical trials and drug development processes
• Ability to read and comprehend complex clinical trial protocols and designs
• Oncology study experience
• 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
• Open to candidates in the following states ONLY: New York, Massachusetts, North Carolina, Connecticut
• Some travel may be required to customer sites 

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

Benefits

Salary

• Hourly range for this position is $50 to $55 per hour
• Available to work 40 hours per week during business hours
• Individual hourly pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training
• Contract until approximately May 30, 2027 (12 months) with possibility of extension 

Benefits

• Retirement Plan (401k)