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

• 
  Develop and implement patient recruitment and retention strategies for clinical trials and programs
  

• 
  Lead and manage trial-related projects and initiatives, ensuring efficient delivery, compliance, and adherence to regulatory and ERB requirements
  

• 
  Make informed, day-to-day decisions by understanding repeatable processes, recognizing nuances, and
  determining
  next steps based on fact-dependent parameters
  

• 
  Partner closely with cross-functional teams and stakeholders to align on strategy, execution, and priorities
  

• 
  Support clinical trial documentation and ensure record-keeping and retention compliance
  

• 
  Operate comfortably in a deadline-driven environment, prioritizing work based on defined processes and associated timelines
  

• 
  Take direction and feedback well, applying learning quickly and
  retaining
  instructions to continuously improve delivery
  

• 
  Apply lessons learned and best practices to improve patient engagement approaches and standardize processes
  

What
We’re
Looking For

• 
  5+ years of clinical trial experience

• 
  3+ years of coordination and/or project management experience supporting clinical or cross-functional initiatives

• 
  3+ years of patient engagement experience, including patient recruitment and retention strategies for clinical trials

• 
  Bachelor’s degree in a scientific or health-related field

• 
  Strong understanding of clinical trial operations, compliance, and regulatory requirements

• 
  Comfortable working across multiple systems and technologies

• 
  Strong communication
  , organization, and collaboration skills

• 
  Passion for improving patient access, diversity, and inclusion in clinical research

Key Requirements for this role:

• 
  Onsite / Hybrid (Indianapolis, IN)

• 
  5+ years of clinical trial experience

• 
  3+ years of patient engagement experience

• 
  Project management and/or clinical coordinator experience

Other Details:

• 
  Schedule: Full Time

• 
  Work Setup: Hybrid in Indianapolis, IN

• 
  Contract Length:
  18 months
  with
  possible contract
  extension