Senior Clinical Research Associate - Oncology

PAREXEL

Remote, Hungary

As a CRA, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. You will participate in the submission of protocols, consent documents for ethics/IRB approval and assist in the preparation of regulatory submissions as requested.

We’ll Expect You To Have

Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
3+ years' experience as CRA.
2+ years' experience in oncology.
Phases II and III experience (Phase IV alone not acceptable).
Preference for solid tumor experience; hematology-oncology also acceptable.
Remote work with 2 days per month in office for AZ meetings.
Location: anywhere in Hungary.
Audit and inspection experience preferred.
Experience in all visit types, focus on monitoring studies in recruitment phase.
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Ability to perform all clinical monitoring activities independently.
Strong interpersonal, written, and verbal communication skills within a matrixed team.
Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
A client-focused approach to work and flexible attitude with respect to assignments/new learning.
The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
An honest and ethical work approach to promote the development of life changing treatments for patients.
Understanding of ICH GCP Compliance.
Excellent time management and social skills
Highly motivated with a phenomenal eye for detail.
Ability to travel domestically and internationally approximately 65%-75% of working time. Expected travelling ~2-3 days/week.
Current driver’s license required.