1

Contract Labcorp Clinical Trials Jobs in Indiana

Clinical trials and research opportunities available Responsibilities * Mostly solid tumor and outpatient duties Compensation * We help negotiate your salary and contract Benefits * Hospital-employed ...

Clinical Research Navigator (Oncology) Contract-to-Hire | Hybrid Schedule We are seeking a Clinical ... Coordinate patient referrals into oncology clinical trials * Communicate with physicians, patients ...

next page

Showing results 1-20

Contract Labcorp Clinical Trials information

What is the difference between Contract Labcorp Clinical Trials vs Clinical Research Associate?

AspectContract Labcorp Clinical TrialsClinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP are commonRequires similar degrees; certifications like CCRP or CRA certification are often preferred
Work EnvironmentContract-based, often in clinical settings or labs, with project-specific durationsUsually in clinical sites or research facilities, monitoring ongoing trials
Employer & IndustryContract labs, pharmaceutical companies, CROsPharmaceutical companies, CROs, research institutions

Contract Labcorp Clinical Trials professionals focus on executing specific clinical trial projects for labs and CROs, often on a contract basis. Clinical Research Associates monitor and manage clinical trials at sites, ensuring compliance and data integrity. While both roles require similar credentials and work in related environments, their responsibilities and employment types differ.

What are the most commonly searched types of Labcorp Clinical Trials jobs in Indiana?

The most popular types of Labcorp Clinical Trials jobs in Indiana are:

What cities in Indiana are hiring for Contract Labcorp Clinical Trials jobs?

Cities in Indiana with the most Contract Labcorp Clinical Trials job openings:

Clinical Trials Manager - Patient Engagement (Direct Portfolio Project Manager) (Hybrid - Indianapol

Pharmavise

Indianapolis, IN • On-site

Contractor

Re-posted 7 days ago


Job description


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