Senior Clinical Research Consultant

Lead Clinical Research Associate with over 15 years qualifying, initiating, monitoring, and closing out Global clinical trials and serving as a mentor for other CRAs.

Seasoned veteran in global clinical monitoring with in depth experience in hematology-oncology and solid tumor indications. Skills include mentoring/training team members, site monitoring, managing all regulatory in house, site initiation visits, and managing all clinical, procedural, and outcome data for oncology therapies.

Relevant Disease Areas

  • Hematology-oncology
  • Breast cancer
  • Lymphoma
  • Pancreatic cancer
  • Leukemia
  • Lung cancer
  • Melanoma

Product Technologies

  • Immunotherapy-monoclonal antibody
  • Biologic
  • Small molecule
  • Combination

Recent Titles

  • Clinical Research Associate Specialist
  • Sr. Clinical Research Associate


  • Greater St. Louis Area
  • Open to remote and in-office

Relevant Companies

  • PPD
  • Provectus
  • Roche

Relevant Skills

  • Managed 9+ investigative sites at one time
  • CRO management, phase I-III clinical monitoring
  • Identifying, evaluating potential investigators
  • Performed all study aspects from study startup through closeout
  • Drug adverse events (safety)
  • Prepared regulatory documents, SOPs
  • CRA mentoring/training
  • Electronic data capture (EDC)

$140 / hr