Senior Clinical Research Associate

Are you looking to grow your career in the Clinical Research space?

Do you have experience or interest in Oncology Clinical Trials?

Are you looking for W/L balance with flexible working hours and other benefits?

If the answer is YES to any of the above questions, this may be the role for you!

This is a full-time, direct hire opportunity for an experienced CRA / Senior CRA. Ideal candidates should have a variety of trial monitoring (field & remote) and full site management experience working in Oncology trials. This position requires flexibility with travel, on average, 8-10 days per month.

Requirements / Qualifications:

At least four years clinical monitoring experience and/or relevant clinical trial experience.
Experience monitoring in Oncology
Relevant life science degree / medical / nursing background, or combination of education and experience.
Skills to mentor and train other CRAs in a positive and effective manner.
In-depth knowledge of clinical trials and the critical elements for success in clinical trials.
Can demonstrate experience and knowledge in the CRO industry that will support POI's management of clinical trials.
Has shown ability to successfully manage people/project issues.
Demonstrates the ability to define and meet project requirements.
Can demonstrate flexibility for improvement and creating solutions.
A thorough knowledge of regulatory submission and reporting requirements and guidelines.
Excellent understanding of the drug development process.

Additional Information:

Comprehensive benefits package
Competitive salaries per location
Departmental Study/Training Budget for furthering professional development
Flexible Working hours
Improved work-life balance
Internal growth opportunities and career progression
Financially rewarding internal employee referral program
Access to online soft-skills and technical training

If you are interested in applying or know someone that may be a good fit, please email me at hweldon@i-Pharmconsulting.com