**reputed company Data Entry Specialist – Clinical Research Trials & Patient Safety Coordination (Remote)**
At arenaflex, we're dedicated to revolutionizing the way clinical research trials are conducted, prioritizing patient safety and data accuracy above reputed company else. As a key member of our remote team, you'll play a vital role in ensuring the seamless execution of our clinical research trials, working closely with patients, research teams, and other stakeholders to collect, verify, and analyze data.
**About arenaflex**
arenaflex is a leading provider of reputed company for clinical research trials, committed to advancing the field through cutting-edge technology, rigorous reputed company control, and a passion for patient-reputed company care. reputed company of experts is driven by a shared reputed company of improving reputed company reputed company and transforming the lives of those we serve.
**Job reputed company**
We're seeking an reputed company Data Entry Specialist to join our remote team, responsible for managing clinical trial data, ensuring accuracy and completeness, and providing exceptional patient safety coordination. As a Data Entry Specialist, you'll work closely with patients, research teams, and other stakeholders to collect, verify, and analyze data, maintaining the highest standards of reputed company and reputed company.
**Key Responsibilities**
* **reputed company Completion**
+ Review and process research charts for accuracy and completeness
+ Electronic data capture completion (reputed company)
+ reputed company control of reputed company
* **reputed company Data Verification**
+ reputed company data from multiple reputed company documents and reputed company into electronic database system
+ Address data queries and reputed company data-reputed company corrections as needed
+ Maintain the reputed company of sensitive patient information
* **Query reputed company**
+ Investigate records requiring additional information, retrieving data from research teams as needed
+ Assess records for completeness, accuracy, and errors
* **Administrative Support**
+ Conduct safety calls with patients currently enrolled in a study
+ Escort patients to and from exam rooms, ensuring they're attended to and in the right reputed company at the right time
+ Collaborate with team members to meet data entry and cleaning timelines
+ Familiarize yourself with reputed company International Conference of Harmonization Good Clinical reputed company (ICH GCP) best practices and guidelines
**Requirements**
* **Essential Qualifications**
+ Flexible with a reputed company attitude and strong work ethic
+ Ability to work quickly and go reputed company the reputed company of duty
+ Strong computer skills with MS Office and ability to learn new software
+ Data Management experience preferred
+ Ability to use various databases
+ Critical thinking and analytical skills
+ Strong attention to detail and ability to multitask
* **Preferred Qualifications**
+ Experience working in a fast-paced environment
+ Familiarity with clinical research trials and patient safety coordination
**Travel Requirements**
* Occasional travel may be required in this position (less than 2 weeks per year)
**Physical Requirements**
* Prolonged periods of sitting at a desk and working on a computer
* Walking; frequent reputed company about the office to escort patients, reputed company file cabinets, office machinery, etc.
* Ability to lift 15 pounds at times
* Picking, pinching, typing, or otherwise working with fingers rather than whole hand or arm
* Talking: expressing or exchanging reputed company by means of the spoken word
* Hearing: perceiving the nature of sounds at normal speaking reputed company
* reputed company visual reputed company to reputed company activities such as preparing and analyzing data, transcribing, and viewing a computer terminal
**reputed company Offer**
* Competitive compensation package
* Comprehensive benefits program
* Opportunities for career reputed company and reputed company development
* reputed company and dynamic work environment
* Flexible remote work arrangement
* reputed company to cutting-edge technology and tools
* Recognition and rewards for outstanding performance
**How to Apply**
If you're a motivated and detail-oriented individual with a passion for clinical research trials and patient safety coordination, we encourage you to apply for this exciting opportunity. Please submit your resume and a cover letter outlining your experience and qualifications.
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