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Clinical Research Associate (Remote) (Northeastern Region)

Remote • Posted 8 hours ago • Updated 8 hours ago

Contract W2

25% Travel Required

Remote

Depends on Experience

Fitment

Dice Job Match Score™

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Job Details

Skills

Medical device
Cardiovascular
Electrophysiology
Pharma monitoring
Clinical trials
FDA regulations
ICH/GCP
Problem-solving
Interpersonal
Communication
Independent work
Multi-tasking
Detail-oriented
Reporting
Stakeholder management
Monitoring

Summary

Please note that this position is a 1 year contract for candidates in the Northeastern U.S. Region. Also, note that this a remote position.

Submit your resume only if you live in Northeastern U.S. Region, other candidates will be rejected.

Requirements

10 - 12 out of office days per month on average, inclusive to travel.
MUST have medical device experience.
Must have extensive experience with: Cardiovascular, Monitoring, and Medical Device.

Experience Requirements

The ideal candidate will have cardiovascular medical device monitoring experience; however, cardiovascular/electrophysiology pharma monitoring experience will be considered OR medical device experience.
4 - 5 years of monitoring experience required.
A Bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.

Candidate Qualifications

In-depth knowledge of FDA regulations and ICH/Google Cloud Platform guidelines.
Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
Ability to work independently and manage multiple priorities in a dynamic environment.
A well-executed plan for communication with the study teams and sites.
Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports.

Position Overview
To support 1 - 3 protocols in the cardiovascular/electrophysiology medical device space.

Candidates must provide their phone number. Job reference code is A5225.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: NETSO
Position Id: A5225
Posted 8 hours ago

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Clinical Research Associate (Remote) (Northeastern Region)

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