Global Feasibility Manager

This is a fully remote position, open to applicants in United States.

📋 Description

• Take charge of the development and implementation of the feasibility strategy in collaboration with clinical programs, study delivery, global study management, and cross-functional data teams.

• Oversee the execution of feasibility strategy plans, including country selection, site identification, timelines, and the synthesis of feasibility insights.

• Direct country and site identification, feasibility assessments, and country selection for clinical studies.

• Collaborate with study team members, data analytics teams, and country teams to carry out global feasibility activities.

• Ensure uniform feasibility execution throughout the portfolio/pipeline and close the gaps between local and central data.

• Align and communicate timelines and expectations between data providers and study teams.

• Coordinate analysis timelines with study team decision milestones, encompassing enrollment timelines, footprint optimization, key assumptions, and patient recruitment strategy.

• Gather local internal and external data on treatment standards, approved/reimbursed treatments, disease incidence/prevalence, patient access, and operational barriers.

• Determine optimal geographic country footprints and recommend clinical study sites.

• Analyze, interpret, and integrate data to deliver feasibility recommendations and support data-driven decision-making.

• Examine trends, identify root causes, and offer actionable recommendations to expedite study execution.

• Facilitate study baseline commitment and change processes at both the country and study levels.

• Initiate and lead global initiatives for continuous improvement in feasibility.

• Assist in the development of systems, processes, and work practices for swift and accurate program and protocol feasibility assessments.

⛳️ Requirements

• Doctorate degree OR

• Master’s degree & 2 years of directly related experience or equivalent OR

• Bachelor’s degree & 4 years of directly related experience or equivalent OR

• Associate’s degree & 8 years of directly related experience or equivalent OR

• High school diploma / GED & 10 years of directly related experience.

• Over 10 years of experience in life sciences or a medically related field, including 6 years of clinical research experience in biopharmaceuticals acquired while working on clinical trials at a biotech, pharmaceutical, or CRO company.

• Experience in feasibility and/or country clinical operations.

• Familiarity with how data and analytics can enhance study design and operational planning.

🏝️ Benefits

• A comprehensive employee benefits package, which includes a Retirement and Savings Plan with generous company contributions.

• Group medical, dental, and vision coverage.

• Life and disability insurance.

• Flexible spending accounts.

• A discretionary annual bonus program.

• Stock-based long-term incentives.

• Award-winning time-off plans.

• Flexible work models, including remote and hybrid work arrangements where feasible.

• Career development opportunities.

• Support for work/life balance.