drjobs Medical Reviewer/Safety Reviewer III

Medical Reviewer/Safety Reviewer III

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
Send me jobs like this
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs
Job Location drjobs

Kearny, AZ - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Job Description:
The Medical Device Safety team is a highly diverse department that plays a critical role in conceptualizing designing and implementing high-priority analytical strategies clinical oversight and initiatives. The team is a high-profile high-impact team that works with PPS functions on a range of product initiatives. As a member of the team you are at the forefront of working with leaders to identify critical priorities and drive high-value projects that make an impact on safety of our patients.
Responsibilities:

  • Assisting with ongoing continuous improvement projects spanning across departmental needs.
  • Responsible for individual and periodic medical device safety reporting.
  • Responsible for PI site notifications.
  • Providing support for training and automation efforts.
  • Support medical safety consultation activities in matters related to risk/benefit and proper product safety usage as needed.
  • Gain understanding of risk management regulations standards and guidance for medical devices and combination products.
  • Biomedical engineer or RN Required.

Requirements:

  • Bachelor of Science in Nursing or Bachelor of Science with Major in Nursing.
  • Proficient in Microsoft Office tools Data Analysis Research Data Automation Case processing of Device SAE/AEs device complaints and SADE potential cases.
  • Knowledge of Research & Development and an understanding of regulatory guidelines / requirements related to R & D Medical Devices / Combination Products (e.g. ICH GCP CFR EU-MDR safety reporting).
  • Clinical Trial Experience.
  • Clinical Trial Device Experience.
  • Knowledge of electronic databases (e.g. Rave EDC Veeva EDC Microsoft Office including Excel Oracle Veeva Salesforce Applications and other database tools.)
  • Ability to effectively interact with and influence others without direct reporting relationships.
  • Ability to multi-task and prioritize while maintaining attention to detail with high quality outputs.
  • Ability to Meet Challenging Milestones with results orientation Skilled.
  • Strategic Decision Making and Negotiation Skilled.
  • Facilitating Change and managing conflicts Skilled.
  • Ability to Problem Solve Independently & with Others - Highly Skilled.
  • Business Organization & Industry Awareness - Highly Skilled.
  • Cross Functional Relationships and communication skills - Highly Skilled.
  • Execution / Results / Process Improvement - Highly Skilled.
  • Background / Required and Preferred Education Level.
  • RN Required (Active licensure).

Additional Information :

All your information will be kept confidential according to EEO guidelines.


Remote Work :

No


Employment Type :

Contract

Employment Type

Contract

Company Industry

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.