Clinical Research Associate (CRA) III

  • location: Lake Forest, IL
  • type: Contract
  • salary: $40 - $47.02 per hour
easy apply

job description

Clinical Research Associate (CRA) III

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. A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, including Humira and Lupron, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you!

 
location: Lake Forest, Illinois
job type: Contract
salary: $40.00 - 47.02 per hour
work hours: 9 to 5
education: Bachelors
 
responsibilities:
  • Member of the global medical affairs evidence solutions medical research support team (clinical team) responsible for processing the intake, review, contracting, activation, conduct and closeout of Investigator Initiated Research and External Collaborative Research studies within Global Medical Affairs.
  • Responsible for assisting Medical Research Supervisor and Evidence Leads in the preparation for scientific medical review of concept and protocol submissions. Provide oversight to approved studies, assuring timely enrollment of patients and retrieval of required document from investigators/study sites, processing workflow status within the study submission and study maintenance system, coordinate drug shipments, prepare payments, receive and route study publications and CSR, perform study closeout activities.
  • Responsible for executing all elements of externally sponsored research in compliance with quality standards (ICH/GCP, Global Regulations, (e.g., drug supply management, ICBs, reviews and approves HCP invoices/ payments against executed contracts) with minimal oversight and guidance.
  • Responsible for management of clinical essential documents and critical regulatory documents for assigned projects/studies to ensure document packets for study start-up are complete and accurate and consistent with the study start-up timeline.
  • Routinely interact with Evidence Leads on assigned projects and in meetings.
  • Supports the preparation of Scientific Review Meetings (Agenda/ Meeting Materials).
  • Supports on audit/ inspection activities for GCP requirements.
  • Responsible for regular updates appropriate for cross-functional team and stakeholders on study status; ensure our CTMS is up to date.
  • Participates in process improvement initiatives.
 
qualifications:
  • At least 4-6 years pharma related research experience
  • Bachelor's degree
  • Knowledge of externally sponsored research (IIS, external research collaborations)
  • Knowledge of clinical study execution
  • Knowledge of Good Clinical Practices and ICH/Guidelines, and/or other Global Regulations
  • Excellent organizational skills, attention to detail, and strong oral and written communications skills
 
skills: 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.

easy apply

get jobs in your inbox.

sign up
{{returnMsg}}

related jobs