Senior Clinical Research Associate

Psi CRO Ag; United States; On-site; USD 85,000 - 110,000; Full time

Job summary

Psi CRO Ag is seeking a Senior Clinical Research Associate to ensure compliance and quality in clinical studies. You will work directly with stakeholders and manage site communications while monitoring timelines and activities.

The ideal candidate has at least 5 years of experience in on-site monitoring in the USA, especially in Oncology. The position requires excellent communication and multitasking skills, and the ability to travel up to 80%.

Qualifications

• Minimum 5 years of independent on-site monitoring experience in the USA.
• Experience in monitoring Phase I-III clinical trials.
• Experience monitoring complex Oncology trials is required.

Responsibilities

• Conduct and report onsite monitoring visits.
• Be responsible for site communication and management.
• Participate in feasibility research.

Skills

On-site monitoring experience in the USA

Communication skills

Problem-solving skills

Ability to multitask

Education

College/University degree in Life Sciences

Tools

MS Office applications

Job description

Job Description

As a Senior Clinical Research Associate 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.

You will:

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup (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
• Be 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 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 all types of monitoring visits in Phase I-III
• Participation in clinical projects as a Senior Monitor
• Experience monitoring complex 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 lead 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 visa for employment or continued employment now or anytime in the future.