Clinical Strategy and Solutions Manager (Temp 12 Months)

Faro; Connecticut; On-site; USD 69,000 - 76,000; Full time

Benefits offered by this job

Retirement Plan (401k)

Job summary

Faro is seeking an experienced Clinical Operations professional to lead oncology trials within the United States. The role requires 5–7+ years in sponsor company clinical operations, strong knowledge of trials, and ability to read complex protocols. Oncology study experience and familiarity with EDC/IRT/CTMS/ePRO/eCOA/eConsent are essential.

Some travel to customer sites may be required. The candidate should hold a Bachelor's degree in physical or life sciences or statistics, reside in NY, MA,

Qualifications

• Bachelor's degree in a physical/life science or statistics discipline.
• 5–7+ years of Clinical Operations at a sponsor company in pharma trials.
• Strong knowledge of clinical trials and drug development processes.
• Ability to read and comprehend complex trial protocols and designs.
• Oncology study experience.
• Familiarity with trial technologies: EDC, IRT, CTMS, ePRO, eCOA, eConsent, TMF.
• Knowledge of regulatory requirements (ICH, GCP, HIPAA, GDPR).
• Excellent cross-functional team collaboration with urgency.

Skills

Team leadership

Attention to detail

Independent work

Communication skills

Problem solving

Adaptability

Education

Bachelor's degree

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 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

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)