Senior Clinical Research Associate at PSI CRO

Montreal, Quebec, Canada -

Full Time

Start Date

Immediate

Expiry Date

12 Mar, 26

Salary

0.0

Posted On

12 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Monitoring, Data Compliance, Communication, Collaboration, Problem-Solving, Oncology, Feasibility Research, Regulatory Support, MS Office, Source Document Verification, Query Resolution, Study Startup, Site Management, Quality Control, Multitasking

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry /on the market, 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 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. Home-based in Quebec, Canada. You will: Conduct and report all types of onsite monitoring visits Be involved in study startup 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 Experience in all types of monitoring visits in Phase II and/or III Participation in clinical projects as a Lead/Senior Monitor Experience in Oncology Full working proficiency in English and French 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 (if applicable) Additional Information Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Responsibilities

As a Senior CRA, you will ensure timelines, targets, and standards of clinical research projects while building relationships with clinical sites and investigators. You will conduct onsite monitoring visits and be involved in study startup and quality control.