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Newton Mendoza
Clinical Data Coordinator
Summary
Highly accomplished Clinical Data Coordinator with 5+ years of experience in managing clinical trials data. Proven expertise in data management, electronic data capture systems, clinical data standards, and data query and analysis. A highly organized and detail-oriented individual with a strong understanding of regulatory compliance and data privacy. Seeking a challenging role where I can leverage my skills to contribute to the success of clinical research programs.
Education
Bachelor’s degree in Clinical Research or a related field
March 2015
Skills
- Clinical Data Management
- Electronic Data Capture (EDC) Systems
- Clinical Data Standards (CDISC)
- Data Query and Analysis
- Statistical Analysis Software (SAS)
- Clinical Trial Management Systems (CTMS)
Work Experience
Clinical Data Coordinator
- Performed data cleaning and validation, ensuring data quality and compliance with regulatory standards
- Generated clinical data reports and visualizations for investigators and clinical project managers
- Participated in study design and protocol development, providing insights on data collection and management strategies
- Worked closely with investigators, clinical research associates, and other stakeholders to ensure data quality and regulatory compliance
Clinical Data Coordinator
- Managed a team of 6 data entry personnel, ensuring accuracy and timeliness of data entry for clinical trials
- Developed and implemented a data management plan for a Phase III clinical trial, resulting in a 20% reduction in data management costs
- Utilized electronic data capture (EDC) systems, such as Medidata Rave and Oracle Clinical, to capture and manage clinical data
- Developed and maintained clinical databases, ensuring data integrity and security
Accomplishments
- Developed and implemented a data validation process that reduced data errors by 45%, ensuring data integrity and accuracy.
- Led a team of data coordinators in the implementation of a new clinical data management system, which streamlined data collection and analysis.
- Collaborated with clinical researchers to design and develop data collection tools that optimized data quality and reduced patient burden.
- Established data monitoring protocols that identified potential issues early on, preventing delays and ensuring data integrity.
- Trained and mentored new data coordinators, ensuring a high level of proficiency in data management best practices.
Awards
- Recipient of the Clinical Data Excellence Award for outstanding contributions to data quality and management.
- Recognition for contributions to the development of data standards and guidelines for clinical research.
- Award for excellence in data management and analysis in a multicenter clinical trial.
- Recognition for outstanding contributions to the field of clinical data management by a professional organization.
Certificates
- Certified Clinical Data Manager (CCDM)
- Certified Electronic Data Capture Specialist (CEDCS)
- Certified Statistical Data Analyst (CSDA)
- Associate Certified Data Manager (ACDM)
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How To Write Resume For Clinical Data Coordinator
- Highlight your expertise in clinical data management and electronic data capture systems.
- Quantify your accomplishments whenever possible, using specific metrics to demonstrate your impact.
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- Tailor your resume to each job you apply for, highlighting the skills and experience that are most relevant to the position.
- Network with professionals in the clinical research field to learn about job opportunities and gain insights into the industry.
Essential Experience Highlights for a Strong Clinical Data Coordinator Resume
- Managed a team of data entry personnel, ensuring the accuracy and timeliness of data entry for clinical trials.
- Developed and implemented a data management plan for a Phase III clinical trial, resulting in a 20% reduction in data management costs.
- Utilized electronic data capture (EDC) systems, such as Medidata Rave and Oracle Clinical, to capture and manage clinical data.
- Developed and maintained clinical databases, ensuring data integrity and security.
- Performed data cleaning and validation, ensuring data quality and compliance with regulatory standards.
- Generated clinical data reports and visualizations for investigators and clinical project managers.
Frequently Asked Questions (FAQ’s) For Clinical Data Coordinator
What is the role of a Clinical Data Coordinator?
A Clinical Data Coordinator is responsible for managing and ensuring the quality of clinical trial data. They work closely with investigators, clinical research associates, and other stakeholders to collect, clean, and analyze data. They also ensure that data is compliant with regulatory standards and that it is securely stored and managed.
What are the qualifications for a Clinical Data Coordinator?
A Clinical Data Coordinator typically needs a bachelor’s degree in Clinical Research or a related field. They also need to have experience in data management, electronic data capture systems, clinical data standards, and data query and analysis.
What are the key skills for a Clinical Data Coordinator?
The key skills for a Clinical Data Coordinator include data management, electronic data capture systems, clinical data standards, data query and analysis, statistical analysis software, and clinical trial management systems.
What is the career outlook for a Clinical Data Coordinator?
The career outlook for a Clinical Data Coordinator is positive. The demand for qualified Clinical Data Coordinators is expected to grow as the number of clinical trials increases.
What is the salary range for a Clinical Data Coordinator?
The salary range for a Clinical Data Coordinator can vary depending on their experience, location, and employer. According to Salary.com, the average salary for a Clinical Data Coordinator in the United States is $75,000.
What are the benefits of working as a Clinical Data Coordinator?
There are many benefits to working as a Clinical Data Coordinator, including the opportunity to make a difference in the lives of others, the chance to work with a variety of people, and the opportunity to learn about new medical treatments and technologies.