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
Location
- 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