Lead Clinical Research Associate at PSI

Elevate your clinical research career with PSI as a Lead Clinical Research Associate. Manage site monitoring and protocols effectively, ensuring data integrity and compliance.

PSI, a renowned Contract Research Organization, seeks a skilled Lead Clinical Research Associate. This role demands a strong background in clinical monitoring, particularly in Oncology and innovative therapies like CAR-T. You will coordinate site feasibility, monitor timelines, implement corrective measures, and ensure adherence to compliance regulations.

Key Responsibilities:

• Coordinate investigator/site feasibility and study startup processes

• Monitor project timelines and patient enrollment for accuracy

• Review monitoring visit reports for compliance and consistency

• Manage query resolution and Central Monitoring observations

• Conduct training for site Investigators and newly promoted Lead CRAs

Requirements:

• Minimum 4 years of site monitoring experience

• Knowledge of US and Canadian regulatory guidelines

• Strong background in Oncology and innovative therapies preferred

• Full working proficiency in English

• Ability to travel up to 65% as needed

Utilize your expertise in clinical research to drive project success and ensure high standards at PSI.
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