Clinical Research Associate (Remote) (Northeastern Region)
Posted 1 week ago by NetSource, Inc.
Negotiable
Undetermined
Remote
Remote
Summary: This role is for a Clinical Research Associate on a one-year contract, specifically targeting candidates located in the Northeastern U.S. Region. The position is remote and requires significant experience in medical devices, particularly in cardiovascular monitoring. Candidates must be prepared for travel and possess a strong understanding of FDA regulations and clinical trial management.
Key Responsibilities:
- Support 1 - 3 protocols in the cardiovascular/electrophysiology medical device space.
- Conduct monitoring with an average of 10 - 12 out of office days per month, inclusive of travel.
- Establish and maintain effective working relationships with site personnel, investigators, and internal teams.
- Implement effective solutions to mitigate risks and identify issues at sites.
- Communicate complex information clearly and concisely to various stakeholders.
- Manage multiple priorities in a dynamic environment.
Key Skills:
- Medical device experience, specifically in cardiovascular monitoring.
- 4 - 5 years of monitoring experience.
- Bachelor's degree in Life Science, Physical Science, Nursing, or Biological Science.
- In-depth knowledge of FDA regulations and ICH/Google Cloud Platform guidelines.
- Strong problem-solving and interpersonal skills.
- Exceptional verbal and written communication skills.
- Ability to work independently and manage multiple priorities.
- Well-versed in clinical trial management.
Salary (Rate): undetermined
City: undetermined
Country: undetermined
Working Arrangements: remote
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
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.