Clinical Strategy and Solutions Manager (Temp 12 Months)

Faro; New York (NY); On-site; USD 69,000 - 76,000; Full time

Benefits offered by this job

Retirement Plan (401k)

Job summary

Faro is seeking a seasoned Clinical Operations professional in the New York area to lead sponsor-driven pharmaceutical trials. You will interpret complex protocols, manage oncology studies, and collaborate across functions while leveraging EDС, IRT, CTMS and related technologies.

Candidates should have 5-7+ years of Clinical Operations experience, strong regulatory knowledge, and be open to travel. This contract role supports multiple sites and demands meticulous leadership and communication.

Qualifications

• Bachelor's degree required in physical or life or statistics.
• 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

Skills

Clinical Operations

Cross-functional teamwork

Regulatory knowledge

Protocol reading

Oncology study experience

Clinical trial technologies

Travel readiness

Education

Bachelor's degree in physical or life sciences or statistics

Tools

EDC

IRT

CTMS

ePRO

eCOA

eConsent

TMF

Job description

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

Requirements

• 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

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)