Clinical Specialist

CompanyWalker Cole International

LocationUnited Kingdom

Posted At1/14/2026

UK Visa Sponsorship Analytics

Occupation Type

Registered specialist nurses

Occupation Code Skill LevelHigher Skilled

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Description

Clinical Specialist – Medical Devices | Remote

Job ID: 89016

A leading medical device manufacturer is expanding its Regulatory & Clinical function and is seeking a Clinical Specialist to support clinical and post-market activities across a global product portfolio.

This role sits at the centre of clinical strategy and delivery, supporting clinical evaluation, PMCF, and human factors engineering (HFE) activities within a highly regulated ISO 13485 and MDR 2017/745 environment. As a Clinical Specialist, you will collaborate closely with Regulatory Affairs, R&D, Quality, Manufacturing, and Marketing to ensure products remain clinically compliant and market-ready throughout their lifecycle.

Your responsibilities as a Clinical Specialist will include:

Leading and supporting clinical evaluation and PMCF activities for medical devices from planning through to final reporting
Managing clinical and HFE studies, ensuring delivery aligns with timelines, budgets, and regulatory expectations
Providing clinical input across product development, design changes, manufacturing updates, and post-market surveillance

Contributing to Clinical Evaluation Reports (CERs), PMCF plans, protocols, and technical documentation

Interpreting global clinical and regulatory requirements, including ISO 13485, MDR 2017/745, FDA, ISO 14155, and ISO 14971

Advising cross-functional teams on clinical data needs to support regulatory submissions and product claims

Identifying clinical risks, usage challenges, and emerging issues, recommending practical mitigation strategies

Supporting updates to clinical procedures, templates, and best practices

Assisting with internal training on clinical and regulatory compliance topics

Working with external partners and vendors where required to deliver clinical activities

To be successful as a Clinical Specialist, you will need:

Experience within a medical devices organisation operating under ISO 13485
Practical knowledge of MDR 2017/745 (and/or MDD), FDA requirements, and clinical standards such as ISO 14155 and ISO 14971
Background in clinical evaluation, PMCF, or related regulatory clinical activities
Strong written skills, with experience preparing clinical documentation and reports

Ability to manage multiple priorities and contribute effectively to cross-functional project teams

Confident communication skills, with the ability to influence and advise technical and non-technical stakeholders

Experience working in fast-paced, regulated environments; international exposure is advantageous

Why join this opportunity?

Work on globally distributed medical devices within a well-established regulatory framework
Gain exposure to full lifecycle clinical strategy, PMCF, and HFE activities
Join a collaborative, forward-thinking clinical and regulatory team
The company supports continuous learning and career progression.

You must have the right-to-work in the United Kingdom and sponorship cannot be offered at this ttime.