Clinical Research Specialist - Minneapolis or Home Based
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REQUIRED QUALIFICATIONS:
Knowledge of:
- Clinical research study processes, study design, and/or protocol management.
- Clinical trial operations procedures and clinical data reporting processes.
- ICH GCP guidance and FDA regulations.
- Microsoft Suite of software products.
- Intermediate project management, training, and conflict skills.
- Quality assurance.
Ability to:
- Demonstrate excellent oral and written communication.
- Manage multiple deadlines and priorities while ensuring quality and timeliness.
- Perform tasks requiring excellent attention to detail.
- Demonstrate independent problem solving.
- Commit to infrequent overnight travel.
Education and/or Experience:
- Bachelor’s degree in scientific or health related field; however, upon evaluation, equivalent related experience and/or education may be substituted for the scientific or health-related degree requirement.
- Minimum of two years’ current experience directly supporting clinical trials either from a site perspective or participating in protocol management from a sponsor perspective.
- PREFERRED QUALIFICATIONS: (Additional qualifications that may make a person even more effective in the role, but are not required for consideration)
- Knowledge of cellular therapies, diseases treated by cellular therapies, disease assessments, and common treatment complications.
- ACRP or SOCRA certification.
Proof of COVID-19 vaccination with acceptable documentation is required for employment. NDMP will consider all requests for medical or religious accommodation.