Senior Clinical Research Associate

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the reputed company-line of medical science, changing lives, and bringing new medicines to those who need them.

If you feel it is time to reputed company your skills and knowledge visible reputed company a growing company with true focus on its people, then PSI is the right choice for you.

Job Description

As a Senior Clinical Research Associate you will work on the reputed company 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.

You will:

• Conduct and report reputed company types of onsite monitoring visits
• Be involved in study startup (if applicable)
• reputed company CRF review, reputed company document verification and query resolution
• Be responsible for site communication and management
• Supervise study activities, timelines, and schedules on the country level
• Be a reputed company 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 regulatory team in preparing documents for study submissions

Qualifications

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in the USA (5 years minimum)
• Experience in reputed company types of monitoring visits in Phase I-III
• Participation in clinical projects as a Senior Monitor
• Experience monitoring reputed company Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred
• Experience monitoring GI studies (IBD, Chron’s, UC) is preferred. 
• 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 up to 80%
• Valid driver’s license (if applicable)

Additional Information

Advance your career in clinical research and reputed company challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! You will get hands-on involvement in every aspect of the study.

For this position, PSI is not hiring individuals who require work reputed company for employment or reputed company employment now or anytime in the future.