Clinical Research Coordinator
Message: Job details
Salary
From $20 an hour
Job Type
Full-time
Contract
Number of hires for this role
1
Qualifications
Bachelor's (Preferred)
Clinical Trials: 1 year (Preferred)
Clinical Research: 1 year (Preferred)
US work authorization (Preferred)
Benefits
Pulled from the full job description
Professional development assistance
Full Job Description
Job Description:
Hello there!
We are Cognitive Leap (http://cognitiveleap.com). Our work is based on latest research in the fields of artificial intelligence, virtual reality, and neuroscience. The team is focused on innovating digital solutions for mental health, specifically ADHD.
As of now, we are developing a Virtual Reality Attention Tracker. Through tracking the user’s attention performance and body movement throughout the VR experience, our AI algorithm can interpret the data and provide an objective and accurate assessment of inattention and hyperactivity.
We are seeking a Clinical Research Coordinator responsible for the execution of clinical trials through clinical monitoring and data collection activities in support of research and development initiatives. It also requires independent work and multi-tasking on multiple innovative projects in the field of digital solutions in cognitive science and neuroscience.
Essential Duties and Responsibilities:
Work independently and collaboratively on intellectually stimulating projects in the field of digital solutions in cognitive science and neuroscience
Co-develop research protocols, plans, workflows, methodologies, reports with collaborating researchers
Establish and maintain regular communication with collaborative research organization
Participate in data collection using our VR device in coordination with other functional teams, i.e., Research and Development
Assist in collection, anonymization/redaction of clinical data and reports
Assist in the validation and QC of clinical study and development database(s)
Able to use or uses electronic data capture system(s) and other monitoring tools to review and ensure accurate and complete clinical data collection, including data/run review
Conduct remote monitoring and on-site interim monitoring activities including but not limited to essential document review, source data verification, informed consent form review, other site documentation and study material accountability, including reagent accountability and completion and review/signoff of site staff proficiency
Prepare and complete monitoring visit reports and letters, and effectively document site communications
Identify and address routine site issues including protocol deviations and communicate any observed study/data trends and proposed resolutions, as applicable
Resolve non-routine site issues in conjunction with the Principal Investigator
Resolve routine and non-routine technical malfunction with engineers and developers
Qualifications:
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the basic knowledge, skills, and/or abilities required:
Education: Bachelor’s Degree in life science, psychology, neuroscience, behavioral science, cognitive science or equivalent
Demonstrate motivation in the field working independently and multi-tasking
Take initiative in pushing forward the frontiers of technology and science development
Demonstrate great attention to detail
Plans and organizes multiple projects with little supervision
Communicate clearly and effectively both orally and in writing with persons having diverse backgrounds of knowledge and experience; Communicate effectively with children and adolescence
Knowledge of clinical monitoring and trial design
Proficient knowledge of technical computer systems
Experiences with Good Clinical Practice (GCP) and FDA regulations
Experiences with Virtual Reality (i.e. HTC, Oculus) preferred, though not required
How To Apply
For more information regarding this Clinical Research Coordinator position, please send your resume, your expected hourly salary and your availability from Apr 2021 to Dec 2021. Please quote reference CRC007 in all correspondence.
Job Types: Full-time, Contract
Pay: From $20.00 per hour
Benefits:
Professional development assistance
Schedule:
8 hour shift
Supplemental Pay:
Bonus pay
COVID-19 considerations:
We will follow the new IRB and FDA policies and procedures for human subjects research responding COVID-19.
Ability to Commute/Relocate:
Dallas, TX (Preferred)
Education:
Bachelor's (Preferred)
Experience:
Clinical Trials: 1 year (Preferred)
Clinical Research: 1 year (Preferred)
Contract Renewal:
Likely
Work Location:
One location
Company's website:
https://www.cognitiveleap.com/
Company's Facebook page:
https://www.facebook.com/cognitiveleap/
Work Remotely:
No
30+ days ago
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