United States
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Job description
Job Summary
The Senior Clinical Research Associate will play a pivotal role in a global, mid-sized Contract Research Organization (CRO) that is dedicated to driving advancements and innovation in clinical research. This position involves supporting the progress of clinical trials aimed at finding cures for various diseases, with a particular emphasis on oncology.
Responsibilities
- Oversee the planning and execution of clinical trials in accordance with regulatory requirements and company protocols.
- Act as a key liaison between the CRO and study sites, ensuring effective communication and collaboration.
- Monitor trial progress, ensuring compliance with study protocols and reporting any deviations.
- Participate in the training of site staff and contribute to the development of study materials.
- Document and report findings accurately, contributing to the overall success of clinical research initiatives.
Qualifications
- A minimum of a bachelor’s degree in a relevant field or a nursing degree.
- Proven experience in oncology clinical research is a must, with a demonstrated understanding of the complexities involved.
- Strong organizational and project management skills to handle multiple trials simultaneously.
- Excellent communication abilities to effectively interact with various stakeholders in the research process.
- Attention to detail and problem-solving skills to address challenges that arise during study execution.
Worldwide Clinical Trials provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
