Patient & HCP Voice in Design Consultant – Pharmaceutical (Indianapolis, IN) – Contract - Mid-level (On-site/Remote)

This is a remote position.

Overview:

From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp

Our Fortune 500 Pharmaceutical client has an exciting opportunity for Patient & HCP Voice in Design Consultant.

There are two (2) consultants needed for this role. One on-site and one remote.

Job Summary:

We are seeking a strategic and detail-oriented Patient & HCP Voice in Design Consultant to join our client’s Clinical Trial Patient Engagement Team. This role will focus on gathering and leveraging patient and healthcare provider (HCP) insights to enhance clinical trial design and engagement. The consultant will oversee vendor-led CoDesign activities while ensuring that the overall project strategy remains aligned with business and research objectives. This position is critical in integrating real-world patient and HCP perspectives into trial development, ultimately improving accessibility, inclusivity, and engagement.

Responsibilities:

• Insights Gathering: Lead efforts to collect and analyze patient and HCP feedback to inform clinical trial design.
• Vendor Collaboration: Manage relationships with external vendors conducting CoDesign activities, ensuring alignment with strategic objectives.
• Project Oversight: Provide leadership and direction for insight-gathering initiatives, ensuring high-quality, actionable data.
• Stakeholder Engagement: Partner with internal teams, researchers, and external collaborators to integrate insights into trial planning.
• Best Practices Implementation: Apply industry best practices to ensure meaningful and ethical engagement with patients and HCPs.
  
  

Qualifications:

• Minimum of 3 years of experience in a clinical research or life sciences role directly focused on patient and HCP engagement, CoDesign methodologies, or clinical trial patient experience.
• Strong project management and stakeholder collaboration skills.
• Familiarity with CoDesign methodologies or user-centered design approaches is required.
• Ability to work with vendors and guide insight-gathering initiatives.
• Excellent communication and analytical skills.
  
  

This role is ideal for someone passionate about amplifying patient and HCP voices in clinical trial design to drive meaningful innovation.

Other Details:

• Schedule: 40 hours/week
• Contract Length: 18 Months with renewal
• On-site for Candidates in Indianapolis, IN and open to remote
  
  

E-Verify Participation :

Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify.