🌎
This job posting isn't available in all website languages

Clinical Research Associate II - Remote

📁
Research & Development
📅
2500003H Requisition #
Thanks for your interest in the Clinical Research Associate II - Remote position. Unfortunately this position has been closed but you can search our 16 open jobs by clicking here.

REQUIRED QUALIFICATIONS:

Knowledge of:

  • Advanced understanding of clinical research study processes, study design and/or protocol management.
  • Proficient knowledge of clinical trial monitoring procedures and clinical data reporting processes.
  • Medical terminology and anatomy/physiology.
  • Computer proficiency, including the use of standard software (word processing, databases, e-mail) and the use of internet.
  • Intermediate project management, training, and conflict resolution skills.
  • Strong time management skills and problem-solving abilities. 

 

Ability to:

  • Demonstrate excellent oral and written communication.
  • Manage multiple deadlines and priorities independently while ensuring quality and timeliness.
  • Perform tasks requiring excellent attention to detail.
  • Demonstrate independent problem-solving and decision-making, with minimal guidance for complex situations.
  • Analyze trends, identify issues, and escalate as appropriate.
  • Adapt to change.
  • Navigate processes and people involved in clinical research, demonstrating organizational awareness and interpersonal skills necessary to complete work efficiently.
  • Must exemplify our NMDP values in a highly professional manner in all settings.
  • Travel 25-50%, both domestic and international, depending on assigned studies. Travel at times may increase up to 70% as required.

 

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 scientific or health-related degree requirement.
  • Minimum of three years of experience in conducting clinical research studies, with at least one year of direct experience in monitoring clinical research studies or managing sites and protocols, either from a sponsor or CRO perspective.

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.
  • Direct experience working at research sites on clinical studies, with or without direct interaction with patients.
  • 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

Previous Job Searches

My Profile

Create and manage profiles for future opportunities.

Go to Profile

My Submissions

Track your opportunities.

My Submissions