PSI CRO is hiring a Senior Clinical Research Associate to work on the frontline of project communication, ensuring timelines, targets, and standards are met. You will build and maintain key relationships with clinical sites and investigators, focusing on subjects’ rights, safety, and well-being, as well as data quality compliance. We are a global company with a true focus on its people.
What You'll Do
- Conduct and report all types of onsite monitoring visits.
- Be involved in study startup activities (if applicable).
- Perform CRF review, source document verification, and query resolution.
- Be responsible for site communication and management.
- Supervise study activities, timelines, and schedules on the country level.
- Serve as a point of contact for in-house support services and vendors.
- Be involved in quality control, such as compliance monitoring and reports review.
- Participate in feasibility research.
- Support the regulatory team in preparing documents for study submissions.
What We're Looking For
- College/University degree in Life Sciences or an equivalent combination of education, training, and experience.
- Minimum of 5 years of independent on-site monitoring experience in the USA.
- Experience in all types of monitoring visits in Phase I-III clinical trials.
- Participation in clinical projects as a Senior Monitor.
- Experience monitoring complex Oncology trials is required.
- Full working proficiency in English.
- Proficiency in MS Office applications.
- Ability to plan, multitask, and work in a dynamic team environment.
- Strong communication, collaboration, and problem-solving skills.
- Ability to travel up to 80%.
- Valid driver’s license (if applicable).
Nice to Have
- Experience with radiopharmaceuticals and/or breast cancer trials.
- Experience monitoring GI studies (such as IBD, Crohn's, UC).
Technical Stack
- MS Office applications.
Work Mode
This is a hybrid position, offering flexibility for office-based or home-based work.
PSI CRO is an equal opportunity employer.
