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Research Assistant Ii - Remote | Wfh
Company | Get.It Recruit - Administrative |
Address | Austin, TX, United States |
Employment type | FULL_TIME |
Salary | |
Category | Human Resources Services |
Expires | 2023-09-02 |
Posted at | 9 months ago |
Are you a detail-oriented, adaptable, and tech-savvy individual? Are you passionate about making a difference in clinical research? If you answered yes, we have an exciting opportunity for you!
About Us
We are an esteemed academic research organization specializing in clinical trial design, oversight, and management. With over three decades of experience and a focus on therapeutic areas like cardiovascular, wound healing, and diabetes, we have successfully contributed to over 150 clinical trials. Our commitment to innovation extends to community health programs that empower people to lead active and healthy lives.
Position Overview
As a Research Assistant II, you will play a vital role in supporting various projects and programs. Your responsibilities will involve assisting different functional areas, including Research Operations, Community Health, Data Management, Quality Control, and more. Collaboration with team members will be key to ensuring the timely completion of deliverables and problem resolution.
Responsibilities
Serve as a floating resource to support project execution and management.
Assist in preparing essential project documentation and contribute to the Trial Master File.
Manage project-specific training administration and tracking.
Collaborate on study material printing, collation, and distribution.
Conduct quality control reviews of project documentation and manage document uploads into the eTMF system.
Act as a primary point of contact for investigational sites and support query management.
Facilitate report generation and participate in centralized monitoring activities.
Qualifications
GED or HS Diploma required; Nursing or bachelor’s degree preferred.
Minimum of 2 years of clinical research or similar experience. Higher degrees may be considered in lieu of experience.
Proficiency in MS Office, particularly in spreadsheet databases and word-processing.
In-depth knowledge of Good Clinical Practice guidelines and applicable FDA and ICH regulations.
Excellent communication, organizational, and multitasking skills.
Strong attention to detail and the ability to thrive in a collaborative environment.
Benefits
We value our team members and offer a comprehensive benefits package, including medical, dental, vision, life, and more. Additionally, we provide a matching 401(k) plan, generous vacation days, flexible work schedules, and fun monthly events that foster team camaraderie.
Compensation
Targeted Compensation: $20.77/hr - $25.00/hr
Join Our Team
Are you ready to take the next step in your career? We invite you to apply directly at our website: Apply Now.
Equal Opportunity Employer
We are proud to be an equal opportunity employer, providing fair employment opportunities to all qualified applicants. We believe in diversity and inclusivity, where selection decisions are solely based on job-related factors.
Learn More About Us
To get to know us better and explore the values we embrace, please visit our website: Company Website.
Note
Successful applicants will be required to pass a background and education verification check.
Make a difference in clinical research - Join us and be part of our exciting journey!
Employment Type: Full-Time
Salary: $ 20.00 25.00 Per Hour
About Us
We are an esteemed academic research organization specializing in clinical trial design, oversight, and management. With over three decades of experience and a focus on therapeutic areas like cardiovascular, wound healing, and diabetes, we have successfully contributed to over 150 clinical trials. Our commitment to innovation extends to community health programs that empower people to lead active and healthy lives.
Position Overview
As a Research Assistant II, you will play a vital role in supporting various projects and programs. Your responsibilities will involve assisting different functional areas, including Research Operations, Community Health, Data Management, Quality Control, and more. Collaboration with team members will be key to ensuring the timely completion of deliverables and problem resolution.
Responsibilities
Serve as a floating resource to support project execution and management.
Assist in preparing essential project documentation and contribute to the Trial Master File.
Manage project-specific training administration and tracking.
Collaborate on study material printing, collation, and distribution.
Conduct quality control reviews of project documentation and manage document uploads into the eTMF system.
Act as a primary point of contact for investigational sites and support query management.
Facilitate report generation and participate in centralized monitoring activities.
Qualifications
GED or HS Diploma required; Nursing or bachelor’s degree preferred.
Minimum of 2 years of clinical research or similar experience. Higher degrees may be considered in lieu of experience.
Proficiency in MS Office, particularly in spreadsheet databases and word-processing.
In-depth knowledge of Good Clinical Practice guidelines and applicable FDA and ICH regulations.
Excellent communication, organizational, and multitasking skills.
Strong attention to detail and the ability to thrive in a collaborative environment.
Benefits
We value our team members and offer a comprehensive benefits package, including medical, dental, vision, life, and more. Additionally, we provide a matching 401(k) plan, generous vacation days, flexible work schedules, and fun monthly events that foster team camaraderie.
Compensation
Targeted Compensation: $20.77/hr - $25.00/hr
Join Our Team
Are you ready to take the next step in your career? We invite you to apply directly at our website: Apply Now.
Equal Opportunity Employer
We are proud to be an equal opportunity employer, providing fair employment opportunities to all qualified applicants. We believe in diversity and inclusivity, where selection decisions are solely based on job-related factors.
Learn More About Us
To get to know us better and explore the values we embrace, please visit our website: Company Website.
Note
Successful applicants will be required to pass a background and education verification check.
Make a difference in clinical research - Join us and be part of our exciting journey!
Employment Type: Full-Time
Salary: $ 20.00 25.00 Per Hour
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