Lead Clinical Research Associate - Contract Position
- Role
- Research
- Experience
- Lead
- Employment
- Contract
The listing doesn't say where it hires from. It may hire in United States (74% confidence). This is an estimate, not an eligibility rule; verify before applying.Signals: employment terms.
No BS summary
Contract Lead Clinical Research Associate for clinical research/CRO work. Needs leadership over CRA/CTA teams and study monitoring/project-management support.
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries.
Our people are the heart of everything we do. We believe great work happens when team members feel valued, supported, and empowered. At ProTrials, you’ll join a collaborative community committed to making a meaningful impact on global health.
We are excited to connect with skilled individuals who share our passion for advancing clinical research with care, integrity, and excellence.
ABOUT THE JOB
ProTrials is seeking a Contract Lead Clinical Research Associate to join our team.
The Contract Lead Clinical Research Associate (LCRA) is responsible for providing direction and leadership to the Clinical Research Associate (CRA) team and Clinical Trial Associate (CTA) assigned to studies. The Contract LCRA ensures accurate and timely initiation, enrollment, conduct, completion, and provides project management support. The Contract LCRA ensures adequate study monitoring resources are in place for the study. The Contract LCRA also identifies quality issues related to clinical monitoring activities, and along with the study team, establishes action plans to address them.
What you'll do
- Providing direction and leadership to the Clinical Research Associate (CRA) team and Clinical Trial Associate (CTA) assigned to studies
- Ensures accurate and timely initiation, enrollment, conduct, completion, and provides project management support
- Ensures adequate study monitoring resources are in place for the study
- Identifies quality issues related to clinical monitoring activities, and along with the study team, establishes action plans to address them
What they require
- Skilled individuals who share our passion for advancing clinical research with care, integrity, and excellence
Benefits
- You’ll join a collaborative community committed to making a meaningful impact on global health
ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries.