We are desiring to recruit a driven Clinical Research Associate - Remote / Telecommute to join our high calibre team at CYNET SYSTEMS in Dallas, TX.
Growing your career as a Full-Time Clinical Research Associate - Remote / Telecommute is a remarkable opportunity to develop competitive skills.
If you are strong in critical thinking, cooperation and have the right commitment for the job, then apply for the position of Clinical Research Associate - Remote / Telecommute at CYNET SYSTEMS today!
Job Description:- Responsible for conducting study monitoring visits (Site Qualification Visit to Close Out Visit) to assess protocol and regulatory compliance per the approved monitoring plan.
- Review and compare source documentation to eCRFs to ensure data is complete and accurate.
- Provide Investigator and study staff training at study initiation and as needed through the course of the trial.
- Review study specific site documents including: regulatory documents, drug accountability logs, training logs, delegation of authority logs.
- Maintain regular communication with assigned sites to support site enrollment, data entry, query resolution, and patient retention.
- Document site visit findings and observations via trip reports and letters.
- Escalate major visit findings as described in the monitoring plan to appropriate study team members.
- Participate in weekly meetings with study team.
Competencies:
- Excellent oral and written communication skills.
- Sound interpersonal skills.
- Ability to work independently.
- Ability to travel up to 50% of time.
- Ability to identify problems and develop solutions.
- Exceptional attention to detail.
- Ability to navigate and utilize multiple online systems and software.
Education and Experience:
- BA or BS in life sciences related field or registered nursing certificate.
- Minimum of 3 years monitoring experience.
- Pain research experience is a plus.
- Must be knowledgeable of clinical trial systems and Microsoft office applications.
- Must have the capability to complete primary duties for multiple studies.
Other Tasks:
- Participate in the site and/or investigator identification, evaluation, and selection processes.
- Attend and participate in investigator and coordinator meetings, as needed.
- Submit monitoring visit expense reports in a timely manner.
- Assist with central monitoring and site management duties.
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Benefits of working as a Clinical Research Associate - Remote / Telecommute in Dallas, TX:
● Excellent Benefits Package
● Continuous Learning Opportunities
● Generous Compensation
No CV Required
How to get there?
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