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For Companies At a Glance
- Tasks: Conduct site visits, ensure compliance, and manage study documentation.
- Company: Join a global CRO dedicated to innovative clinical research and improving lives.
- Benefits: Enjoy remote work flexibility, career development opportunities, and a supportive team culture.
- Why this job: Make a real impact on patient lives while collaborating with diverse experts in a dynamic environment.
- Qualifications: Requires 2+ years of clinical monitoring experience and a relevant degree in life sciences.
- Other info: Embrace a diverse and inclusive workplace that values creativity and collaboration.
The predicted salary is between 36000 - 60000 £ per year.
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!
What Clinical Operations Does at Worldwide
At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it\’s ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you\’ll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us Worldwide!
What you will do
- Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits
- Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
- Actively participate in study team and investigator meetings
- Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)
What you will bring to the role
- Excellent interpersonal, oral, and written communication skills in English and local language
- Superior organizational skills with attention to detail, and the ability to work independently
- Broad understanding of clinical research principles and process
- Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
- At least two years of independent clinical monitoring experience
- Demonstrable experience in handling multiple protocols across a range of therapeutic indications
- Four-year college curriculum in life sciences, OR Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree)
- Ability to meet the travel requirements of the job
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide !For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn .
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We’reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law. #J-18808-Ljbffr
Senior Clinical Research Associate - UK - Remote employer: Worldwide Clinical Trials
Contact Detail:
Worldwide Clinical Trials Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate - UK - Remote
✨Tip Number 1
Familiarise yourself with the latest trends and developments in clinical research, especially in the therapeutic areas mentioned in the job description. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the role.
✨Tip Number 2
Network with current or former employees of Worldwide Clinical Trials on platforms like LinkedIn. Engaging with them can provide valuable insights into the company culture and expectations, which can be beneficial during your application process.
✨Tip Number 3
Prepare to discuss specific examples from your previous experience that showcase your ability to handle multiple protocols and your attention to detail. Being able to articulate these experiences clearly will set you apart from other candidates.
✨Tip Number 4
Research the company's mission and values thoroughly. Be ready to explain how your personal values align with theirs, particularly regarding diversity and inclusion, as this is a key aspect of their workplace culture.
We think you need these skills to ace Senior Clinical Research Associate - UK - Remote
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical monitoring and showcases your understanding of clinical research principles. Emphasise any specific therapeutic areas you've worked in, as this aligns with the role's requirements.
Craft a Compelling Cover Letter: Write a cover letter that reflects your passion for improving lives through clinical research. Mention how your values align with Worldwide Clinical Trials' mission and culture, and provide examples of how you've contributed to team success in previous roles.
Highlight Communication Skills: Since excellent communication is crucial for this role, ensure you provide examples of how you've effectively communicated with diverse teams and stakeholders in your application. This could include experiences from meetings, presentations, or written reports.
Showcase Organisational Skills: Demonstrate your superior organisational skills by detailing how you've managed multiple protocols or projects simultaneously. Use specific examples to illustrate your attention to detail and ability to work independently.
How to prepare for a job interview at Worldwide Clinical Trials
✨Understand the Company Culture
Before your interview, take some time to research Worldwide Clinical Trials. Familiarise yourself with their mission and values, especially their commitment to diversity and inclusion. This will help you align your answers with their culture during the interview.
✨Showcase Your Experience
Be prepared to discuss your previous clinical monitoring experience in detail. Highlight specific projects you've worked on, particularly those that involved multiple protocols or therapeutic areas. This will demonstrate your capability and adaptability in the role.
✨Prepare for Technical Questions
Expect questions related to clinical research principles and processes. Brush up on your knowledge of regulatory submissions, TMF management, and EDC systems. Being able to speak confidently about these topics will show your expertise and readiness for the position.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready to ask your interviewers. Inquire about the team dynamics, opportunities for professional development, or how they support work-life balance. This shows your genuine interest in the role and the company.
