Adrienne Leach

I am a highly motivated healthcare professional with a solid foundation as a Certified Medical Assistant and extensive experience as a Clinical Research Assistant. Over the years, I’ve built a well-rounded skill set that bridges direct patient care with the regulatory, administrative, and data-driven responsibilities of clinical research.

My journey began in clinical settings, where I gained hands-on experience working alongside physicians and nurses, providing compassionate and efficient care to diverse patient populations. As I transitioned into clinical research, I brought that same attention to detail, empathy, and work ethic to support studies across various therapeutic areas.

In my current role as a Clinical Research Assistant, I have supported multiple phases of clinical trials, from patient recruitment and informed consent to data collection, regulatory compliance, and study documentation. I thrive in fast-paced environments and am adept at coordinating with cross-functional teams, sponsors, and regulatory bodies to ensure the integrity and success of each study.

I’m seeking opportunities where I can continue to grow within the research or healthcare field—ideally in environments that value both clinical expertise and research precision. Whether in a site-based or remote role, I bring reliability, professionalism, and a commitment to improving patient outcomes through ethical and efficient research.

Experienced healthcare professional with a background as a Certified Medical Assistant and extensive hands-on experience as a Clinical Research Assistant. Skilled in both patient care and clinical trial operations, including subject recruitment, informed consent, data collection, regulatory compliance, and study coordination. Proven ability to work collaboratively with cross-functional teams and adapt in fast-paced research environments.

Committed to advancing clinical outcomes through ethical, organized, and high-quality research support.

Certified Medical Assistant with formal training in clinical procedures, patient care, and medical office administration. Completed Good Clinical Practice (GCP) certification, demonstrating a solid understanding of regulatory and ethical guidelines in human research. Ongoing commitment to professional development through healthcare and research-focused courses, with hands-on experience supporting clinical trials across multiple therapeutic areas.