Patient Engagement Lead

🕒 September 24

🌐 United States, United Kingdom – Remote

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🌲 North Carolina – Remote

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💵 $90k - $178k / year

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

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👻 Ghost score 0%

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Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Support strategic feasibility assessments during proposal phases, including Study Burden Analysis and Patient and Site insights • Develop bespoke Patient and Site support strategies and articulate their value propositions • Present at bid defenses and client meetings as needed • Develop and maintain collaborative relationships with internal stakeholders • Capture, collate, and share patient experience data and insights to inform strategy and planning • Evaluate Patient Pathway and trial burden for new study opportunities and communicate associated risks and support needs • Maintain and develop strategic relationships with Patient Advocacy groups in assigned therapy areas • Incorporate indication-specific representation and inclusion aspects into strategic customer recommendations • Build FDA Diversity Action Plans, UK Patient and Public Involvement projects, and other patient engagement projects • Maintain relationships with external vendors providing Patient and Site engagement, recruitment, and retention support services • Translate patient engagement strategies into operational and tactical plans with project teams • Establish metrics and measure the impact of patient and site support strategies on clinical trial delivery performance • Maintain industry trend knowledge and communicate potential impacts to stakeholders • Perform other duties as assigned

🎯 Requirements

• Minimum Bachelor’s degree or equivalent • 8+ years’ transferrable experience in medical, healthcare, scientific or related field • Preference for experience in Patient engagement, recruitment & retention, feasibility or site-study coordination research roles • Knowledge of the principles of Good Clinical Practice • Competent computer skills in MS Word, Excel, and PowerPoint • Effective written and spoken English communication skills • Basic understanding of clinical drug development across a broad range of therapeutic areas • Ability to think creatively and solve problems • Ability to challenge effectively, influence, and build/maintain relationships with senior stakeholders • Ability to process information quickly and dynamically adapt to new information • Accomplished negotiation and presentation abilities • Ability to work at a fast pace with short timelines and minimal oversight • Ability to work collaboratively with other functions in pre- and post-award settings • Ability to function as part of a remote team • Excellent organizational skills • May require travel (<10%) for business needs

🏖️ Benefits

• Competitive benefits package depending on location • Remote work arrangement • Inclusive and equitable workplace • Pay equity and transparency

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