Full-Time

Clinical Research Coordinator 1

Cancer Center

Posted on 10/1/2025

St. Louis University

St. Louis University

No salary listed

St. Louis, MO, USA

In Person

Category
Biology & Biotech (2)
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Requirements
  • Associate’s degree or an allied health professional degree in an appropriate area and one year of relevant experience; or an equivalent combination of education and experience
  • Knowledge of GCP, SOPs, FDA and other regulatory requirements is required
  • Basic knowledge of Clinical Research Coordinator core responsibilities
  • Knowledge of the principles of research design
  • Excellent written and verbal communication skills
  • Excellent interpersonal/human relations skills
  • Excellent organizational and analytical skills
  • Attentiveness to detail
  • Ability to maintain confidentiality
  • Ability to operate personal computer and various software packages
Responsibilities
  • Participate in day-to-day operations of clinical research studies conducted by SLU principal investigator(s); perform a variety of duties involved in the collection, compilation, documentation, and analysis of clinical research data
  • Collects, prepares, processes, ships, and maintains the inventory of research specimens, primarily those requiring complex procedures
  • Knowledgeable in regulatory and institutional policies and processes; applies appropriately in study documentation, protocol submissions, and standard operating procedures (SOPs). Develops or helps develop SOPs. Leads meetings that are multidisciplinary, including those with complex objectives
  • Serves as the backup liaison with sponsors, Research Pharmacy, and other parties as necessary. Is responsible for all aspects of managing and documenting Investigational Product (IP); including arrival, storage, tracking, and provision to research participants. Prepares for and provides support for study monitoring and audit visits, including support for the reviewer. Addresses and corrects findings
  • Performs other duties as assigned

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