Seeking a Clinical Research Associate (CRA) position where my extensive knowledge of clinical trial processes, attention to detail, and strong analytical skills can contribute to ensuring regulatory compliance, data integrity, and the overall success of clinical research projects. Eager to apply my experience in monitoring, site management, and protocol adherence to support the advancement of innovative therapies while maintaining the highest standards of quality and patient safety.

University of California, Riverside

El Camino College

North Torrance High School

I am working closely with Principal investigators, physicians, study sponsors, and other research staff to maintain accurate documentation. Managing clinical trials from start to finish, including patient visits, monitoring, auditing activities, and trial close-out. Serving as a primary contact for study subjects and overseeing patients' progress throughout the trial. Managing the day-to-day operations of clinical trials with patient contact, by coordinating patient’s visits, collecting/recording data, and reporting adverse events. Conducting initial screenings and obtaining informed consent from prospective participants. Collecting and recording data from study participants, ensuring accurate and timely documentation of study procedures, reporting adverse events, and any other relevant information. Maintains investigational drug accountability.

Clinical Research Coordinator

Collaborating with investigators and study sponsors to develop research protocols, including study design, objectives, and methodology. Develop study documentation, including informed consent forms, case report forms, and study manuals. Explain the study details, risks, and benefits to potential patients and obtain informed consent. Collect patient record study data, including patient’s medical histories, laboratory results, and other relevant information. Communicating with participants regarding study objectives, measuring vital signs, and performing 12-lead ECG on site. Maintaining research records of study activity, including case report forms, drug dispensation records, and other regulatory forms. Update patient records, data entry into multiple electronic databases, and scheduling patients. Update study sites and complete data entry with relevant information as the study progresses.

Clinical Research Study Coordinator

Provide the highest level of customer service. Utilize a professional level of sales and service to maximize sales performance. Demonstrate a comprehensive knowledge of luxury merchandise.

Stylist

Greet customers promptly and genuinely and re-engage appropriately. Serve, delight, and engage with customers. Build customer loyalty by creating genuine connections with customers and followed all interaction protocols while helping the member with their payments.

Retail Associate

Advancing medical knowledge and improving patient care by valuable exposure to the intricacies of laboratory work, strengthened my technical skills, and fostered my passion for scientific inquiry. Restocked lab supplies cleaned patient space and equipment, and prepared beds for the patients. Answered phones and sent reminders to patients for their upcoming appointments.

Lab Volunteering Experience

Performing Arts Certificate

Certificate Principles of Bio Medical Science

Introduction to Pharmacy Technician

Nithya Bamunuarachchi

English

Native or bilingual proficiency

Spanish

Limited working proficiency

Hindi

Elementary proficiency

Singhalese

CEO / Managing director of California Medical Research Associates Inc. (CMRA)

I am a Principal Clinical Associate; Nithya and I have been working together on two projects for nearly two years now; she is my assigned primary Clinical Research Coordinator at a research site.
I've witnessed Nithya's rapid and impressive growth and development in her current role during this time. Her intellect, drive, and work ethic are all top-notch. 
I see her as someone who would continue to grow and excel, whether in her current role, moving up internally, or moving to a different organization. She not only performs at a very high level but has tremendous potential should she choose to move into a position entailing greater responsibility.

Clinical Research Associate

Douglas Cooper

Documentation

Risk Management

Quality Assurance

Project Management

Vendor Management

Data Analysis

Communication

Time Management

Negotiation

Budget management

Data Management

Auditing

Technical Writing

Quality Control

Critical Thinking

Medical Terminology

Risk assessment

Regulatory compliance

Clinical monitoring

Site management

Problem-Solving

Clinical Trials

Medical Writing

Protocol Review

Regulatory Submissions

Protocol Writing

Study Coordination

Gcp Compliance

Protocol Adherence

Site Monitoring

Adverse Event Reporting

Subject Recruitment

Protocol Compliance

Investigator Training

Gcp Knowledge

Gcp (Good Clinical Practice)

Clinical Trials Knowledge

Conflict Resolution

Emotional Intelligence

Leadership

Time management

Interpersonal Skills

creativity

Organization

Self-Motivated

Critical thinking

Networking

Teamwork

Adaptability

patient care

Teamwork and Collaboration

Excellent communication skills

Certified in Cardiopulmonary Resuscitation (CPR) and First Aid

EKG/ECG administration

Research skills and laboratory proficiencies

Clinical Knowledge

Measuring vital signs

Nithya Bamunuarachchi

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