Clinical Research Monitor

Irvine, CA, USA

Full-TimeDepends on ExperienceSenior LevelMasters

Job Description

Edwards Lifesciences is looking for an experienced Clinical Research Monitor with an attention to detail and excellent communication skills to join our team. The Clinical Research Monitor is a critical member of the clinical trial team and will be responsible for ensuring that clinical trials are conducted in accordance with applicable regulations and the study protocol. The ideal candidate for this position will have a background in clinical research, extensive knowledge of Good Clinical Practices (GCPs) and ICH guidelines, and experience in the medical device or pharmaceutical industries. This position requires excellent organizational skills, the ability to manage multiple tasks simultaneously, and the willingness to take initiative. We are looking for a self-motivated individual with the ability to work both independently and collaboratively to ensure the successful completion of clinical trials.

Responsibilities:

Ensure clinical trials are conducted in accordance with applicable regulations and the study protocol.
Follow Good Clinical Practices (GCPs) and ICH guidelines.
Maintain accurate records of all clinical trial activities.
Monitor and assess the quality of clinical trial data.
Communicate effectively with the clinical trial team to ensure the successful completion of clinical trials.
Assist in the preparation of regulatory submissions and documents.
Assist in the development and implementation of clinical trial plans.
Manage multiple tasks simultaneously and take initiative to ensure successful outcomes.
Collaborate with other members of the clinical trial team and external partners to ensure the quality and accuracy of data.
Keep up to date with industry guidelines and regulations.

Where is this job?

This job is located at Irvine, CA, USA

Job Qualifications

Good Communication Skills
Ability To Manage Complex Projects
Analytical And Problem Solving Skills
Knowledge Of Relevant Regulations
Ability To Collect And Analyze Data
Ability To Interact With Different Stakeholders
Understanding Of Medical Terminology And Protocols
Good Organizational And Time Management Skills

Required Skills

Documentation
Risk Management
Quality Assurance
Training
Data Analysis
Communication
Time Management
Clinical Research
Scheduling
Problem Solving
Negotiation
Regulatory compliance
Organization
Monitoring
Professionalism

Soft Skills

Communication
Leadership
Time management
Interpersonal Skills
creativity
Organization
Critical thinking
Teamwork
Adaptability
Problem-Solving

Compensation

According to JobzMall, the average salary range for a Clinical Research Monitor in Irvine, CA, USA is $50,000 to $100,000 per year. This range may vary depending on the size of the employer, the qualifications of the individual, and the location of the position.

Additional Information

Edwards Lifesciences is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Required LanguagesEnglish

Job PostedNovember 9th, 2023

Apply BeforeMay 22nd, 2025

This job posting is from a verified source.

Reposted

See an issue with this job? Report it to us