Clinical Research Associate

Job title: Clinical Research Associate

Department: Research & Development

Location:Southampton UK

GLS: T02

Working hours: 37.5 hours per week Mon-Fri

A brighter future awaits you

What to expect:

Responsible for coordination administration and regulatory compliance of clinical trial documentation and investigational product traceability for the conduct of clinical trials during product research and development of ophthalmic medical device (Contact Lens). Also works with clinical partners investigative sites and CROs.

Essential Functions & Accountabilities:

• Ensure coordination between the UK and US R&D teams for clinical studies including study management site management study documentation and study product management.
• Ensures compliance with Good Clinical Practices (GCP) SOPs and applicable regulations with particular emphasis on document control device accountability and site monitoring.
• Establishes and maintains study binder to ensure complete and accurate records of all clinical study documentation.
• Organizes distributes tracks files and archives all clinical study documentation including protocols CRFs clinical reports product traceability adverse event tracking and communications with institutional review board/ethics committee and clinical investigators ensuring timely completion of milestones.
• Coordinates and manages the flow of documents and study materials between Sponsor and clinical sites related to the conduct of clinical trials during contact lens (medical device) product development.
• Manages site training and maintain agreements site visit & training logs.
• Ensures robust interactions between Sponsor and study site personnel to prevent address and resolve issues
• Manages Clinical Inventory including sourcing/ordering shipping receiving transfer traceability and destruction of investigational and commercial products (medical devices) used in clinical studies.
• Liaises and works with CROs in the initiation of required studies.
• Coordinates Sponsor in-house clinical studies (scheduling and enrolling subjects preparing the CRFs subject compensation and data entry).
• Coordinates schedules and performs a program of clinical study monitoring as appropriate via remote or on-site document and data review to ensure study site compliance with GCP SOPs study protocols and applicable regulations.
• Coordinates and documents all study related activities including informed consent development IRB/EC approval study start-up enrollment data management and closeout.
• SOP and work-instruction development as applicable.
• Coordinates clinical trial associate (CTA) personnel activity as required.
• Performs required clinical study or administrative tasks as assigned by the clinical trial manager.

About you:

Experience:

• Minimum 2 years experience in clinical research operations previous experience as a Clinical Research Associate (CRA) preferred.
• Experience of working with CROs preferred.

Knowledge Skills and Abilities:

• Excellent administrative organizational and study oversight skills
• Strong attention to detail with a systematic meticulous work approach to work
• Excellent verbal and written communication skills including appropriate use of medical and scientific terminology
• Proven ability to work effectively to deadlines and manage competing priorities in a fastpaced environment
• Strong crossfunctional collaboration skills with experience working closely with clinical operations data management regulatory quality and other stakeholders
• Demonstrated ability to quickly assimilate interpret and apply new information
• Working knowledge of computer operating systems (e.g. CTMS/EDC/eTMF systems)
• Strong Excel and database management skills including data tracking reconciliation and reporting
• Well-organizedwithability to multitask and adjust to changing priorities
• Medical and technical aptitude; experience or knowledge in ophthalmic medical devices is desirable
• Professional demeanour with a high level of integrity and accountability

Education:

• Bachelors degree biological sciences or medical/scientific-related field (or equivalent experience) required.
• BS or MA in Clinical Trial Management (or equivalent) preferred
• ACRP Certification (or equivalent) is highly desirable

What we offer:

Youll receive competitive compensation and a fantastic benefits package including 25 days holiday pension scheme healthcare cover life assurance access to our Wellness Platform to support you in mental health and wellbeing a discounted contact lens scheme and much more!

We are committed to our employees personal and professional development and offer extensive training to support your career growth and help every individual to reach their full potential. To help us achieve our goals well give you everything you need to help you achieve yours.

We also provide access to LinkedIn Learning to help you develop in you career and grow with CooperVision

If you like what you see take the first step towards your Brighter Future and apply today!All suitably qualified applicants will receive equal consideration and opportunities from CooperVision

Please view our careers page at view all other opportunities.

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