Strategic Clinical Solutions Leader (Oncology)

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

Benefits offered by this job

401k

Job summary

Faro in Massachusetts seeks an experienced Clinical Operations professional to lead sponsor-driven pharmaceutical trials, focusing on oncology studies and regulatory compliance.

The role requires reading complex protocols, using trial tech (EDC/CTMS/ePRO), and partnering across teams to deliver study goals, with travel to customer sites as needed. A Bachelor’s degree and 5–7+ years of relevant experience are required; open to candidates in NY, MA, NC, CT.

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

Team leadership

Attention to detail

Independent or group work

Communication skills

Problem solving

Goal-oriented

Education

Bachelor's degree

Tools

EDC

IRT

CTMS

ePRO

eCOA

eConsent

TMF

Job description

Faro in Massachusetts seeks an experienced Clinical Operations professional to lead sponsor-driven pharmaceutical trials, focusing on oncology studies and regulatory compliance.

The role requires reading complex protocols, using trial tech (EDC/CTMS/ePRO), and partnering across teams to deliver study goals, with travel to customer sites as needed. A Bachelor’s degree and 5–7+ years of relevant experience are required; open to candidates in NY, MA, NC, CT.