Clinical Research Associate II/I at PSI CRO

Daxing District, Beijing, China -

Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

0.0

Posted On

10 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Monitoring, Communication, Collaboration, Problem-Solving, Site Management, Regulatory Support, Feasibility Research, MS Office Proficiency, Source Document Verification, Query Resolution, Audit Preparation, Inspection Participation, Travel Ability, Teamwork, English Proficiency, Mandarin Proficiency

Industry

Pharmaceutical Manufacturing

Description

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 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them. If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. Based in Shanghai/Beijing Job Description As a Clinical Research Associate II/I 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 SSV, 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 At least 2 years of independent on-site monitoring experience in China Experience in all types of monitoring visits in Phase II and/or III Therapeutic area experience in Oncology is a plus Full working proficiency in English and Mandarin 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 70% of time Additional Information Advance your career in clinical research, overseeing a variety of tasks and growing with the company. You will work closely with driven and dedicated cross-functional teams, get all support and ownership of your projects. Excellent working conditions Extensive training and friendly, collegial team Competitive salary package Opportunities for personal and professional growth

Responsibilities

As a Clinical Research Associate II/I, you will conduct and report various onsite monitoring visits and perform CRF review and source document verification. You will also manage site communication and support internal project teams regarding study progress.