Clinical Research Associate (Remote) (Northeastern Region)
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.
Requirements
ā¢ 10 - 12 out of office days per month on average, inclusive to travel.
ā¢ MUST have medical device experience.
ā¢ Must have extensive experience with: Cardiovascular, Monitoring, and Medical Device.
Experience Requirements
ā¢ The ideal candidate will have cardiovascular medical device monitoring experience; however, cardiovascular/electrophysiology pharma monitoring experience will be considered OR medical device experience.
ā¢ 4 - 5 years of monitoring experience required.
ā¢ A Bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
Candidate Qualifications
ā¢ In-depth knowledge of FDA regulations and ICH/Google Cloud Platform guidelines.
ā¢ Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
ā¢ Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
ā¢ Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
ā¢ Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
ā¢ Ability to work independently and manage multiple priorities in a dynamic environment.
ā¢ A well-executed plan for communication with the study teams and sites.
ā¢ 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 A5243.
Submit your resume only if you live in Northeastern U.S. Region.
Requirements
ā¢ 10 - 12 out of office days per month on average, inclusive to travel.
ā¢ MUST have medical device experience.
ā¢ Must have extensive experience with: Cardiovascular, Monitoring, and Medical Device.
Experience Requirements
ā¢ The ideal candidate will have cardiovascular medical device monitoring experience; however, cardiovascular/electrophysiology pharma monitoring experience will be considered OR medical device experience.
ā¢ 4 - 5 years of monitoring experience required.
ā¢ A Bachelor's degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science.
Candidate Qualifications
ā¢ In-depth knowledge of FDA regulations and ICH/Google Cloud Platform guidelines.
ā¢ Strong problem-solving skills to mitigate risks and identify issues at sites and implement effective solutions promptly.
ā¢ Strong interpersonal skills to establish and maintain effective working relationships with site personnel, investigators, and internal teams.
ā¢ Exceptional verbal and written communication skills, with the ability to convey complex information clearly and concisely.
ā¢ Ability to tailor communication style to the needs and preferences of different stakeholders, fostering a collaborative environment.
ā¢ Ability to work independently and manage multiple priorities in a dynamic environment.
ā¢ A well-executed plan for communication with the study teams and sites.
ā¢ 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 A5243.