I.V. and Blood withdrawal

I’m a dedicated Clinical Research Coordinator with a strong background in managing clinical trials, ensuring regulatory compliance, and working closely with patients and research teams. I have experience supporting Phase I–IV studies, streamlining processes, and keeping studies on track. I'm passionate about clinical research and always looking for ways to contribute to meaningful advancements in patient care.

Arizona State University

Casa Loma College

Los Angeles Community College District

As CRC II, I mentor and train new clinical research staff, have in depth knowledge of clinical research, methods and solve complex problems. I assist the site, manager or team lead with strategic initiatives to help drive growth at the site.
Lead multiple studies at once across multiple therapeutic indications and serve in the delete unblinded role.

Clinical Research Coordinator II

As a Utilization Review Nurse, I evaluated patient medical records to ensure that healthcare services are medically necessary, cost-effective, and meet established standards. I also collaborate with healthcare providers, insurance companies, and patients to review treatment plans, authorize services, and ensure compliance with regulations and guidelines. Additionally, I identify opportunities for improved patient care and resource utilization.

Utilization Review Nurse

As a Senior Research Nurse, I lead and coordinated clinical research projects, ensuring compliance with protocols and regulatory requirements. My responsibilities included data collection, and analysis, as well as providing expert nursing care and support to research participants. I collaborated with multidisciplinary teams, mentored junior staff, and contributed to the development of study protocols. My role was critical in advancing clinical research and improving patient outcomes. Qualifications included a nursing degree, clinical research experience, and strong organizational and communication skills.

Senior Research Nurse

As a Senior Clinical Research Coordinator, I oversaw and managed clinical trials, ensuring compliance with regulatory requirements and study protocols. Responsibilities included supervising study staff, mentoring/ Training new CRCs, managing data collection, and maintaining accurate documentation. The role required strong organizational skills, and the ability to liaise with investigators, sponsors, and regulatory bodies.

Senior Clinical Research Coordinator

Cynthia Torres

English

Spanish

Native or bilingual proficiency

Documentation

Risk Management

Quality Assurance

Communication Skills

Project Management

Vendor Management

Data Analysis

Communication

Time Management

Contract Negotiation

Budget management

Data Management

Quality Control

Data collection

Team Leadership

Risk assessment

Regulatory compliance

Analysis

Organization

Site management

Laboratory Techniques

Problem-Solving

Good Clinical Practice

Clinical Trials

Ethics

Medical Writing

Patient Recruitment

Protocol Development

Protocol Review

Informed Consent

Clinical Operations

Protocol Management

Study Coordination

Regulatory Submission

Protocol Adherence

Training And Education

Site Monitoring

Site Visits

Adverse Event Reporting

Study Monitoring

Irb Submissions

Subject Recruitment

Monitoring Visits

Study Management

Site Identification

Investigator Training

Good Clinical Practice (GCP)

Site

Site Initiation

Feasibility Assessment

Investigator Meeting

Conflict Resolution

Emotional Intelligence

Leadership

Multitasking

Time management

Interpersonal Skills

self-motivation

Critical thinking

Networking

Attention to detail

Teamwork

Adaptability

Conflict Resolution<|Endoftext|><|Endoftext|><%#

Cynthia Torres

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