Clinical Strategy and Solutions Manager (Temp 12 Months)

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) #J-18808-Ljbffr Faro