Clinical Trials Manager – Patient Engagement (Direct Portfolio Project Manager) (Hybrid – Indianapolis, IN) Contract with Possible Extension
Pharmavise Corporation.com
Office
Indianapolis, United States
Contract
Our Fortune 500 Pharmaceutical client has an exciting opportunity for a Clinical Trials Manager.
Job Summary:
We are seeking a Clinical Trials Manager – Patient Engagement to develop and deliver patient recruitment and retention strategies across clinical trial programs. This role combines strategic thinking, hands-on project management, and deep clinical trial experience to support patient-centered, compliant, and efficient trial execution.
This is a strong fit for someone who has worked closely in clinical trials, has coordinated or managed trial projects, and has directly supported patient engagement, recruitment, and/or retention efforts.
What You’ll Do
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Develop and implement patient recruitment and retention strategies for clinical trials and programs
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Lead and manage trial-related projects and initiatives, ensuring efficient delivery, compliance, and adherence to regulatory and ERB requirements
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Make informed, day-to-day decisions by understanding repeatable processes, recognizing nuances, and determining next steps based on fact-dependent parameters
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Partner closely with cross-functional teams and stakeholders to align on strategy, execution, and priorities
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Support clinical trial documentation and ensure record-keeping and retention compliance
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Operate comfortably in a deadline-driven environment, prioritizing work based on defined processes and associated timelines
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Take direction and feedback well, applying learning quickly and retaining instructions to continuously improve delivery
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Apply lessons learned and best practices to improve patient engagement approaches and standardize processes
What We’re Looking For
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5+ years of clinical trial experience
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3+ years of coordination and/or project management experience supporting clinical or cross-functional initiatives
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3+ years of patient engagement experience, including patient recruitment and retention strategies for clinical trials
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Bachelor’s degree in a scientific or health-related field
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Strong understanding of clinical trial operations, compliance, and regulatory requirements
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Comfortable working across multiple systems and technologies
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Strong communication , organization, and collaboration skills
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Passion for improving patient access, diversity, and inclusion in clinical research
Key Requirements for this role:
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Onsite / Hybrid (Indianapolis, IN)
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5+ years of clinical trial experience
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3+ years of patient engagement experience
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Project management and/or clinical coordinator experience
Other Details:
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Schedule: Full Time
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Work Setup: Hybrid in Indianapolis, IN
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Contract Length: 18 months with possible contract extension
