About the Company
ICON plc is a global provider of drug development solutions and services to the pharmaceutical, biotechnology, and medical device industries. We specialize in the strategic development, management and analysis of programs that support clinical development – from compound selection to Phase I-IV clinical studies. With a global footprint and a commitment to innovation, ICON is dedicated to improving patient lives by accelerating the development of new treatments. We foster a collaborative and inclusive work environment where employees are empowered to grow their careers and make a real impact.
Job Description
We are seeking an enthusiastic and dedicated Clinical Research Associate (CRA) to join our dynamic team in Bromley. This pivotal role involves monitoring clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and regulatory requirements. This is an exciting opportunity for a CRA looking to advance their career with a leading global CRO, and we are pleased to offer a comprehensive global relocation package for eligible candidates ready to contribute to groundbreaking research. You will be responsible for managing clinical trial sites throughout the study lifecycle, from site initiation to close-out, ensuring data integrity and patient safety.
Key Responsibilities
- Conducting pre-study, initiation, routine monitoring, and close-out visits for assigned clinical trial sites.
- Ensuring compliance with study protocols, Standard Operating Procedures (SOPs), GCP, and applicable regulatory requirements.
- Verifying the accuracy and completeness of case report forms (CRFs) and source documents.
- Managing site performance to ensure timely subject recruitment and data submission.
- Providing training and guidance to site staff on study protocols and procedures.
- Identifying, documenting, and resolving site-related issues and escalating as appropriate.
- Preparing comprehensive visit reports and other required documentation in a timely manner.
- Participating in investigator meetings and other project-related discussions.
- Acting as a primary point of contact for assigned clinical sites.
Required Skills
- Minimum of 2 years of independent clinical monitoring experience (site visits).
- Strong understanding of ICH-GCP guidelines and relevant regulatory requirements.
- Excellent communication, interpersonal, and organizational skills.
- Ability to work independently and manage multiple priorities effectively.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Valid driver’s license and ability to travel extensively (up to 70%) within the UK and potentially internationally.
- Fluent in English (written and spoken).
Preferred Qualifications
- Bachelor’s degree in a life science, nursing, or related health field.
- Experience across various therapeutic areas, especially Oncology, Central Nervous System, or Rare Diseases.
- Previous experience with remote monitoring techniques and electronic data capture (EDC) systems.
- Demonstrated ability to mentor junior CRAs.
Perks & Benefits
- Competitive annual salary and performance-based bonuses.
- Comprehensive global relocation package, including visa support and settlement assistance.
- Generous paid time off, including public holidays and annual leave.
- Private medical and dental insurance.
- Life assurance and disability benefits.
- Pension scheme with company contributions.
- Ongoing professional development opportunities and career advancement programs.
- Employee assistance program for personal and professional support.
- Flexible working arrangements (where applicable) and a supportive work culture.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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