Enable job alerts via email!

Clinical Research Associate II

PSI CRO

Oxford

Remote

GBP 60,000 - 80,000

Full time

7 days ago
Be an early applicant

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

An established industry player is seeking a Clinical Research Associate II to enhance their innovative team. In this remote role, you will be pivotal in ensuring the success of clinical research projects by managing relationships with clinical sites and stakeholders. Your expertise in monitoring visits and compliance will be crucial in safeguarding subjects’ rights and data integrity. This role offers the opportunity to work on diverse therapeutic indications while being supported by a company that values professional development and employee well-being. Join a forward-thinking organization that is committed to quality and excellence in clinical research.

Qualifications

  • BSc or MSc in Life Sciences or equivalent experience required.
  • Independent on-site monitoring experience in the UK is essential.

Responsibilities

  • Conduct onsite monitoring visits and manage site communication.
  • Support quality control and participate in feasibility research.

Skills

Written Communication
Verbal Communication
Problem-Solving
Collaboration
Planning
Multitasking

Education

BSc in Life Sciences
MSc in Life Sciences

Tools

MS Office

Job 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.

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.