Clinical Research Associate II - Hybrid/Remote
Thanks for your interest in the Clinical Research Associate II - Hybrid/Remote position.
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REQUIRED QUALIFICATIONS:
Knowledge of:
- Clinical research study processes, study design and/or protocol management.
- Clinical trial monitoring procedures and clinical data reporting processes.
- ICH GCP guidance and FDA regulations.
- Medical terminology and anatomy/physiology.
- Microsoft Suite of software products.
- Intermediate project management, training, and conflict resolution skills.
Ability to:
- Perform tasks requiring excellent attention to detail.
- Manage multiple deadlines and priorities while ensuring quality and timeliness.
- Work effectively and efficiently in a remote environment.
- Travel up to 70% of time (domestic and international).
Education and/or Experience:
- Bachelor degree in healthcare/science related field.
- Minimum of two years’ experience monitoring clinical research studies and/or protocol management according to ICH GCP/FDA guidelines or verifying clinical data from medical records.
PREFERRED QUALIFICATIONS: (Additional qualifications that may make a person even more effective in the role, but are not required for consideration)
- Functional knowledge of cellular therapies, diseases treated by cellular therapies, disease assessments, and common treatment complications.
- ACRP or SOCRA certification.
Due to the recent Executive Order, proof of COVID-19 vaccination with acceptable documentation is required for employment. NDMP will consider all requests for medical or religious accommodation.