Job Details

Title: Senior Clinical Research Associate
Company: PSI CRO
Location: Home-Based (USA)

As a Senior CRA you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Responsibilities:

-Conduct and report all types of onsite monitoring visits
-Perform CRF review, source document verification and query resolution
-Responsible for site communication and management
-Supervise study activities, timelines, and schedules on the country level
-Point of contact for in-house support services and vendors
-Involvement in quality control, such as compliance monitoring and reports review
-Participate in feasibility research
-Support regulatory team in preparing documents for study submissions

Qualifications:
-College/University degree in Life Sciences or an equivalent combination of education, training & experience
-Minimum 5+ years of independent on-site monitoring experience in the USA
-Experience in all types of monitoring visits in Phase II and/or III
-Participation in clinical projects as a Lead/Senior Monitor
-Experience monitoring Oncology clinical trials required
-Full working proficiency in English
-Proficiency in MS Office applications
-Ability to plan, multitask and work in a dynamic team environment
-Communication, collaboration, and problem-solving skills
-Ability to travel

To apply for this position or for more information, please contact: Kimberly.Bernstein@psi-cro.com

SOCRA Exp: 3/5/2021