Clinical Research Associate I - Minneapolis or Home-Based
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REQUIRED QUALIFICATIONS:
Knowledge of:
- Clinical research study processes, study design and/or protocol management.
- Medical terminology and anatomy/physiology.
- Microsoft Suite of software products.
- Training and conflict resolution skills.
Ability to:
- Perform tasks requiring excellent attention to detail.
- Communicate clearly and effectively to staff and site personnel through oral and written formats.
- 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).
- Must exemplify our Be The Match Standards.
Education and/or Experience:
- Bachelor degree in healthcare/science related field. However, upon evaluation, equivalent related experience and/or education may be substituted for the degree requirement.
- Minimum one year experience monitoring clinical research studies and/or protocol management according to GCDMP/ICH GCP/FDA guidelines or verifying clinical data from medical records.
- On evaluation, one year previous experience in a Senior Clinical Data Analyst, Clinical Research Coordinator III, or equivalent position within the CIBMTR/NMDP may be substituted for the experience requirement.
PREFERRED QUALIFICATIONS: (Additional qualifications that may make a person even more effective in the role, but are not required for consideration)
- Knowledge of blood and marrow transplant clinical research and medical field.
- ACRP or SOCRA certification.