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 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)