Clinical Research Associate II at PSI CRO

Oxford, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

30 Aug, 26

Salary

0.0

Posted On

01 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

On-site Monitoring, Clinical Research, CRF Review, Source Document Verification, Site Management, Regulatory Documentation, Oncology, MS Office, Problem Solving, Collaboration, Multitasking, Communication Skills

Industry

Pharmaceutical Manufacturing

Description

Company Description PSI is a leading Contract Research Organisation with more than 25 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 CRA II, 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. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance. This is a remote role. Your responsibilities will include: Conducting and reporting all types of onsite monitoring visits Driving the study startup phase (if applicable) Performing CRF reviews, source document verification and query resolution Be responsible for site communication and management Supervising study activities, timelines, and schedules for each site Acting as a point of contact for in-house support services and vendors Supporting quality control, such as compliance monitoring and reports review Participating in feasibility research Supporting the regulatory team in preparing documents for study submissions and regulatory approval Qualifications BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience Independent on-site monitoring experience in the UK, ideally on multiple projects at a time Demonstrable experience in all types of monitoring visits in Phase II and/or III Strong written and verbal communication skills Experience supporting Oncology studies is beneficial, but not essential Intermediate to Advanced knowledge of MS Office Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills are essential As you will be monitoring multiple sites, you must have a full and clean driver's license, and the ability to travel. 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. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.

Responsibilities

The CRA II is responsible for conducting onsite monitoring visits and managing relationships with clinical sites and investigators. They ensure data compliance, subject safety, and the adherence to project timelines and standards.