Clinical Research Auditor I - remote

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 approximately 35 - 50%, both domestic and international, depending on audit schedule. Travel at times may increase up to 70% as required.
• Must exemplify our NMDP Standards.

Education and/or Experience:

• Bachelor’s 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 of 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.

BENEFITS:
NMDP offers regular, full-time employees medical, dental, vision, life and disability, accident/critical illness/hospital, well-being, legal, identity theft and pet benefits. Retirement, paid time off/holidays, leave and incentive plans are also offered to eligible employees. Please reference this link for more information: NMDP Benefit Information