Project Coordination resource II

  • location: Northbrook, IL
  • type: Contract
  • salary: $30 - $35 per hour
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job description

Project Coordination resource II

job summary:
As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We are currently partnering with a company known for their leading clinical trials as well as Research & Development. With the goal to constantly develop innovative products, you will feel secure in the fact that you are making a difference. Apply for your dream job now!

 
location: Northbrook, Illinois
job type: Contract
salary: $30 - 35 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
  • Support the onboarding of FSP resources for the CS organization including system access, training matrix maintenance and compliance, oversight metrics / dashboard development, and oversight manual maintenance
  • Provide operational support for CoE related activities, including implementation and sustainability of the global operating model, patient centricity related activities, and CS business process optimization
  • Support creation of quality and timely executive summaries/updates for Sr. Leadership as it relates to COE deliverables
  • Provide administrative, project management and system related support for the COE
  • Provide administrative support related to contracts including tracking /monitoring of contracting activities; CDAs & Contracts (obtaining signatures / mailing originals)
 
qualifications:
  • BA/BS degree with at least three years clinical trial experience or equivalent
  • Must have excellent interpersonal, written and verbal communication skills, administrative skills and computer ability with a demonstrated ability to multi-task
  • Strong Excel and Word skills required
  • Fluent in English
  • This is an onsite position
  • Experience working with CROs
  • Ability to use internal systems to pull required clinical contracts (CTAs)
  • Worked with CTAs, CDAs and MTCAs (Types of contracts)
Preferred:

  • Knowledge of ICH/GCP guidelines and regulatory requirements.
  • Knowledge of clinical drug development processes
  • Project Management skills
  • Experience with development and implementation of process improvement initiatives
  • Experience working with Clinical Research Organizations and/or other clinical trial related vendors
  • Notary
 
skills: Project Management, MS-WORD, MS-EXCEL, GCP (Good Clinical Practice), ICH Regulations
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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