Medical Reviewer/Safety Reviewer III Job at Katalyst Healthcares & Life Sciences, Kearny, NJ

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  • Katalyst Healthcares & Life Sciences
  • Kearny, NJ

Job Description

  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

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.

Job Tags

Contract work, Immediate start,

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