Clinical Trials Co-ordinator

We are looking for a highly motivated and enthusiastic individual who is interested in clinical research to join our world leading cystic fibrosis (CF) clinical trials team, located close to the vibrant King’s Road in Chelsea.

As a Clinical Trials Co-ordinator you will play an integral role in the delivery of high quality research which could range from infants through to adults with CF. You will be required to work collaboratively with the clinical team and wider multi-disciplinary team supporting an exciting portfolio of commercial and academic led clinical trials; making a valued contribution in assessing and managing the care pathways for patients participating in research. This will involve supporting the identification, recruitment, education and monitoring of patients participating in research along with the timely collection and documentation of accurate data.

The post requires you to have excellent communication skills, an ability to understand and comply with clinical protocols, and the ability to work autonomously. We will provide all the necessary training.

**Duties and responsibilities**:

- Identification and recruitment of potential participants for research studies in cystic fibrosis and other inherited respiratory conditions
- Provision of front-line support to study participants by phone or in the clinic, demonstrating politeness, courtesy and sensitivity and ensuring any enquiries are dealt with or followed up
- Performance and review of clinical assessments, collection and processing of blood or other samples from participants
- Maintenance of accurate and complete records of all findings, demonstrating awareness and compliance with local policies, procedures, guidelines and standards at all times
- To maintain up-to-date skills and knowledge in the field of cystic fibrosis and clinical trials and attend national and international conferences to continue professional development and develop areas of personal interest within healthcare.
- Contribution in the writing of research reports and publications

**Essential requirements**:

- You must hold a university/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
- Experience of working directly with patients / study participants in a clinical setting is essential and experience of working with children is desirable
- A good understanding of clinical terminology is required, and ideally in respiratory physiology
- You must have proven experience of organisational, record keeping, and time management skills, accurate data management, knowledge of handling confidential information and an understanding of current legislation and requirements
- Excellent written and oral communication skills and computer literacy are essential
- You must have the ability to work independently, effectively and flexibly as part of a team-unit and cooperate in the accomplishment of departmental goals and organisational objectives

**Further information**:
This is a Full Time and Fixed Term role for 12 months based at the Royal Brompton Campus.

**Documents**:

- JD - Clinical Trial Coordinator - RS.pdf