The Lead Clinical Research Associate (LCRA) at ProTrials Research, Inc. provides leadership and direction to Clinical Research Associates (CRAs) and Clinical Trial Associates (CTAs) on assigned studies. This role ensures the accurate and timely execution of clinical trial activities, including study initiation, enrollment, conduct, and completion, while supporting project management and monitoring resource planning.
What You'll Do
- Provide direction and leadership to the Clinical Research Associate (CRA) team and Clinical Trial Associate (CTA) assigned to studies
- Ensure accurate and timely initiation, enrollment, conduct, and completion of clinical trials
- Provide project management support for clinical studies
- Ensure adequate study monitoring resources are in place for the study
- Identify quality issues related to clinical monitoring activities
- Collaborate with the study team to establish action plans to address quality issues
Benefits & Compensation
- Join a collaborative community helping to build a healthier world
- Balance a meaningful workload with life’s everyday moments
- Work that contributes to groundbreaking treatments and solutions in pharmaceutical, biotechnology, and medical device industries
- Be part of a company committed to employee happiness, health, and success
Team & Environment
- Committed to helping patients, caregivers, and loved ones
- Focused on doing work that matters
- Values collaboration and building a healthier world
- Supports work-life balance to keep employees happy, healthy, and successful
- Demonstrates experience, quality, and integrity in clinical research services
