Clinical Research Associate

At ConvaTec, our vision is to develop pioneering trusted medical solutions to improve the lives we touch. We are a global medical technology business focused on serving people and care givers in the areas of advanced wound care, ostomy care, continence and critical care and infusion care. We devise, develop and manufacture innovative products and services that support people with deeply personal and challenging medical conditions, helping to improve care for them and giving them greater confidence, freedom and mobility.

We are guided by our five core values, that shape the way we work, every day: Improve Care, Deliver Results, Grow Together, Own It and Do What’s Right. We are a global Group, with over 9,900 employees and in 2020, our Group generated revenues of over $1.894 billion.

Every day, our products improve the lives of millions of people around the world. We're hugely proud of this, which is why we're transforming our business to reach millions more. Join us as a Clinical Research Associate and you'll drive progress that really means something.**About the role**:
You’ll be responsible for performing activities related to the execution of studies in support of ConvaTec’ s sponsored clinical trials while maintaining a high level of quality and integrity of data analysis. The CRA supports all day-to-day activities of clinical studies and trials.

Our successful CRA can be based anywhere in the UK and will be expected to travel between 25-50% of the time. All travel and any hotel stays will be expensed as per our company policy.

Duties and Responsibilities:

- The day-to-day conduct of the ConvaTec studies
- Liaising with CRO and Investigators
- Reporting of adverse events and device malfunctions as per ConvaTec’s procedures
- Working with the Clinical Project Manager on the implementation of EDC, CTMS and eTMF for use in the studies
- Raising Purchase Order requests
Administering clinical trials according to good clinical practices (GCPs) and standard operating procedures (SOPs)
- Ensuring all Non-Disclosure Agreements (NDAs) are in place with relevant external parties
- Provide general logístical support for the clinical trials such as the provision and shipment of study supplies
**Qualifications and Competencies required**:

- Medical experience desirable, previous clinical study experience essential
Good written and verbal communication skills are also required to work as a CRA, as is an ability to multitask
- Communicates and works closely with the Clinical Project Manager and Regulatory Affairs to ensure timely completion of the studies
- Highly organised and detail-oriented, a problem-solver with strong analytical and research skills
- Ability to multi-task and support several projects as dictated by the needs of the business
- An understanding of scientific or clinical research and methods is desirable
- Should have an interest in math and statistics
- Proactive and be willing to work independently

Our transformation will change your career. For good. You'll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you'll be supported to bring them to life. There'll be challenges. But stretch yourself and embrace the opportunities, and you could make your biggest impact yet.

This is stepping outside of your comfort zone.

This is work that'll **move** you.

**#LI-LT2**

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**Equal opportunities**
ConvaTec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.

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