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Senior Clinical Research Associate
PSI CRO
Source: Headcount Labs · original listing ↗
Job data: Headcount Labs, ODbL 1.0. Job descriptions belong to their employers.
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About this role
Company Description PSI is a leading Contract Research Organization with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry. You will: * Conduct and report SIV, RMV, COV onsite monitoring visits * Perform CRF review, source document verification and query resolution * Be responsible for site communication and management * Be a point of contact for in-house support services and vendors * Communicate with internal project teams regarding study progress * Participate in feasibility research * Support regulatory team in preparing documents for study submissions * Prepare and particiapte on audits and inspections Qualifications * College/University degree in Life Sciences or an equivalent combination of education, training & experience * Independent on-site monitoring experience * Experience in all types of monitoring visits in Phase II and/or III * Experience in Oncology is a plus * Full working proficiency in English and French is essential. * 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 * Valid driver’s license Additional Information This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.