Clinical Research Associate (CRA) – ICON Plc
| Job Title | Clinical Research Associate (CRA) |
|---|---|
| Company | ICON Plc |
| Location | United Kingdom |
| Salary | £42,865 (~₹46 lakhs per year) |
| Experience | 2+ years (Oncology trials preferred) |
| Education | B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences |
| Key Responsibilities | On-site trial monitoring, compliance with GCP, study site management |
| Job Highlights | Work/Life Balance, Flexibility, Problem Solving, Time Management |
| Application | Email CV to Gayathri.Nareshkumar@iconplc.com with subject: “CRA Application – Oncology Expertise” |
| Verified Job | Yes |
Join the Global Leader in Clinical Research: ICON plc
Working at ICON plc, a world-renowned Clinical Research Organization (CRO), means being part of a leading company that pushes the boundaries of clinical research excellence. With a presence in over 40 countries, ICON collaborates with top biopharmaceutical and medical device companies, providing cutting-edge solutions that speed up the development of life-saving treatments.
As a Clinical Research Associate (CRA) at ICON, you will contribute directly to advancing global healthcare by managing clinical trials and ensuring high standards of patient safety and data integrity. If you are passionate about clinical research and have a knack for problem-solving, this is the role for you. Clinical Research Associate (CRA) – ICON Plc
Key Responsibilities of a Clinical Research Associate (CRA)
In this role, you’ll be responsible for monitoring clinical trials in the UK, particularly in the field of oncology. Your day-to-day tasks will include:
- On-Site Monitoring: Visiting clinical trial sites to ensure protocols are followed and patient safety is upheld.
- Compliance Oversight: Ensuring that all study sites adhere to ICH-GCP (Good Clinical Practice) guidelines and relevant regulatory requirements.
- Data Accuracy: Collaborating with site staff to confirm that clinical data is accurate and documentation is maintained to the highest standards.
- Problem-Solving: Identifying and resolving issues at trial sites to ensure smooth trial execution.
- Communication: Regularly reporting on trial progress to the project team and sponsor, ensuring that updates are clear and actionable.
This role offers a great opportunity for you to play an active part in clinical research while sharpening your organizational, problem-solving, and time management skills. Clinical Research Associate (CRA) – ICON Plc
Qualifications and Experience Required
To qualify for the Clinical Research Associate role at ICON, you must meet the following criteria:
- Experience: At least 2 years of on-site monitoring experience in oncology or related therapeutic areas.
- Educational Background: A bachelor’s degree in Life Sciences, Pharmacy, or related fields such as B.Pharm, M.Pharm, Pharm.D, or M.Sc.
- Knowledge: A strong understanding of Good Clinical Practice (GCP) guidelines and clinical trial protocols.
- Work Authorization: You must have a valid UK work permit to apply for this role.
If you have previous experience working within a sponsor-dedicated model, it will be considered an advantage. Clinical Research Associate (CRA) – ICON Plc
What Skills Make a Successful CRA?
Being a successful CRA at ICON requires a combination of technical knowledge and interpersonal skills. Some of the key skills that will help you excel in this role include:
- Strong Communication Skills: You’ll need to liaise effectively with trial site staff and sponsors to ensure the smooth operation of the trial.
- Organizational Abilities: Managing multiple tasks and ensuring that all trials run on time requires strong organizational and time management skills.
- Attention to Detail: Every piece of data collected in clinical trials must be accurate, and it’s your job to ensure that this happens.
- Analytical Thinking: You’ll need to think critically to identify and resolve any site-related issues that arise during the trial.
- Technological Proficiency: Familiarity with clinical trial software and documentation tools will be highly beneficial in managing the data. Clinical Research Associate (CRA) – ICON Plc
Why Choose ICON Plc?
Working at ICON gives you the opportunity to make a meaningful impact on global healthcare. Not only will you be contributing to the development of groundbreaking new treatments, but you’ll also enjoy a work-life balance, flexibility, and opportunities to grow your career in clinical research.
If you are passionate about advancing healthcare through innovative clinical research, then this role offers the perfect blend of professional growth and personal fulfillment. Clinical Research Associate (CRA) – ICON Plc
How to Apply
If this role excites you and you meet the qualifications, don’t miss out on this opportunity. To apply for the Clinical Research Associate position at ICON Plc:
- Prepare Your Application: Send your CV and a cover letter that highlights your relevant experience.
- Subject Line: Make sure to include “CRA Application – Oncology Expertise” in the subject line of your email.
- Email: Submit your application to Gayathri.Nareshkumar@iconplc.com.
Apply soon, as this highly competitive position is likely to fill quickly. This is your chance to contribute to global healthcare solutions and grow your career with one of the best in the industry! Clinical Research Associate (CRA) – ICON Plc
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