Joanna Dederko

Clinical Research Associate with 21 years of experience: 1 year of experience as a Drug Depot Coordinator, 5 years of experience as a CRA and 15 years of experience as a Senior CRA and Senior CRA II.

Worked on about 30 Clinical trials in different Therapeutic areas (see the Clinical Trial Experience section), phases I-IV in both adult and pediatric population.

Experienced with clinical trial management from start to finish. Utilizes strategic planning and regulatory acumen to uphold compliance and project integrity.

Performed all types of Monitoring Events: PSV, SIV, IMV and COV.

Familiar with Start Up activities

Played an active role within the clinical team in the team work to help reach project goals, achieve deliverables, and meet project timelines.

Displays strong written and oral communication skills.

Proactive and goal-oriented professional with good time management and problem-solving skills.

Demonstrates strong analytical, communication, and teamwork skills, with proven ability to quickly adapt to new environments.

• PPD CRA Academy, 2020
• Clinical Foundation Program, 2019
• Fundamentals of Clinical Research, 2004

• Hematology/Oncology
• Genitourinary
• Respiratory
• Rare Genetic Diseases
• Renal and Urinary Disorders
• Cardiology/Vascular Diseases
• Dermatology
• Digestive
• Endocrinology/Metabolic Diseases
• Musculoskeletal
• Psychiatry/Psychology/Mental Disorders
• Vaccine

• AIM methodology
• Risk Based Monitoring
• Compliance with ICH/GCP requirements
• Scale/Patient Reported Outcome Measure
• Audit Experience (as on site Monitor)
• Computer Experience: Different Clinical and/or client specific systems for trial management, such as EDC, CTMS, IVRS, IWRS, eDiaries, AGMednet, ePro, Medidata, Lab Portals, MS Office (Word, Excel, Nitro, PowerPoint, Teams)

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