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- Tasks: Lead clinical trials, ensuring compliance and monitoring progress to improve patient outcomes.
- Company: Join Johnson & Johnson, a leader in healthcare innovation dedicated to making a difference.
- Benefits: Enjoy a competitive salary, flexible work environment, and career development opportunities.
- Why this job: Make a real impact on health by developing the medicines of tomorrow.
- Qualifications: BA/BS in Life Sciences and 3 years of clinical trial monitoring experience preferred.
- Other info: Be part of a supportive team that values diversity and individual contributions.
The predicted salary is between 48000 - 72000 £ per year.
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
We are searching for the best talent for a driven Senior Site Manager, United Kingdom to serve as the primary contact point between the Sponsor and the Investigational Site for trials in phases 2-4. In other organisations, the Senior Site Manager may be known as Senior Clinical Research Associate or Monitor. We are hiring for several therapeutic areas; preferably the candidate will have experience in Neuroscience, Respiratory, Retinal, Immunology or Oncology. The head office location is in High Wycombe, Buckinghamshire, UK (relocating to Maidenhead Oct 2026) and this position is home-based with up to 50% travel.
Purpose:
The position is across various therapeutic areas and will include monitoring a variety of trials in different indications. As a Senior Site Manager, you will be responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure. Our new colleague should be flexible and is able to work independently. We are seeking to hire a strong communicator, a quick learner, a problem solver, and a real team player.
You will be responsible for:
- Activities ranging from site feasibility and selection over site initiation and start-up, to preparation and conduct of site monitoring, oversight of key performance indicators and site/study close-out in complex clinical trials.
- The implementation of a site-level analytical risk-based monitoring model and for working with the site to ensure timely resolution of issues and deviations identified during monitoring visits.
- Ensuring the accuracy and completeness of all trial data including safety data. Managing timely data entry and query resolution in collaboration with site staff.
- Co-creating site-level recruitment and retention strategies and implementation of mitigation actions in partnership with other functional areas.
- Ensuring full documentation of trial related activities in all study files; communicates site and study progress and issues to the Local Trial managers and central study teams.
- Being the local expert in assigned protocols and build the necessary therapeutic area knowledge.
- Coaching or mentoring less experienced colleagues.
- You may participate to process improvement and training. Leads and/or participates in special initiatives as assigned. May assume additional responsibilities or special initiatives such as 'Champion' or 'Subject Matter Expert'.
Qualifications / Requirements:
- BA/BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience).
- A minimum 3 years of clinical trial monitoring experience is preferred, however, other relevant working experiences and skills may be considered by the hiring manager.
- Strong proven understanding of GCP, local laws, and regulations.
- Strong IT skills in appropriate software and company systems.
- Strong team member and self-starter with the ability to work independently.
- Strong communication and influencing skills to effectively manage study sites both remotely and face-to-face.
- Willingness to travel up to 50% (up to 2-3 days per week) with occasional overnight stay away from home.
- Proficient in local language(s) and English. Good written and oral communication skills.
Benefits
We offer a competitive salary and extensive benefits package. The health and well-being of our employees is a priority, we have a flexible working environment as we value work-life balance. We offer career development opportunities for those who want to grow and be part of our organization.
Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform important job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Johnson & Johnson is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us, internal employees contact AskGS to be directed to your accommodation resource.
Senior Site Manager,X-TA in High Wycombe employer: J&J Family of Companies
Contact Detail:
J&J Family of Companies Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Site Manager,X-TA in High Wycombe
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. You never know who might have the inside scoop on job openings at Johnson & Johnson or other companies.
✨Tip Number 2
Prepare for interviews by researching the company and its values. Understand their mission in healthcare innovation and think about how your experience aligns with their goals. This will help you stand out as a candidate who truly gets what they’re about.
✨Tip Number 3
Practice your answers to common interview questions, but keep it natural. Use the STAR method (Situation, Task, Action, Result) to structure your responses, especially when discussing your clinical trial monitoring experience. This will help you articulate your skills effectively.
✨Tip Number 4
Don’t forget to follow up after your interviews! A simple thank-you email can go a long way in showing your appreciation and keeping you top of mind. Plus, it’s a great opportunity to reiterate your enthusiasm for the role at Johnson & Johnson.
We think you need these skills to ace Senior Site Manager,X-TA in High Wycombe
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Site Manager role. Highlight your experience in clinical trials, especially in the therapeutic areas mentioned like Neuroscience or Oncology. We want to see how your background aligns with our mission at Johnson & Johnson.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about healthcare innovation and how you can contribute to our team. Be sure to mention specific experiences that demonstrate your problem-solving skills and ability to work independently.
Showcase Your Communication Skills: As a Senior Site Manager, strong communication is key. In your application, give examples of how you've effectively managed relationships with study sites or collaborated with teams. We love seeing candidates who can clearly convey their ideas and influence others.
Apply Through Our Website: Don't forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re serious about joining our team at Johnson & Johnson.
How to prepare for a job interview at J&J Family of Companies
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical trials, especially phases 2-4. Familiarise yourself with Good Clinical Practice (GCP) and the specific therapeutic areas mentioned in the job description, like Neuroscience and Oncology. This will show that you're not just interested but also well-prepared.
✨Showcase Your Communication Skills
As a Senior Site Manager, you'll need to communicate effectively with various stakeholders. Prepare examples from your past experiences where you've successfully managed relationships or resolved conflicts. This will demonstrate your ability to influence and collaborate with site staff and trial managers.
✨Be Ready for Problem-Solving Questions
Expect questions that assess your problem-solving skills. Think of scenarios where you've had to tackle unexpected issues during a trial. Be ready to explain your thought process and how you arrived at a solution, as this role requires quick thinking and adaptability.
✨Emphasise Teamwork and Independence
This position requires both teamwork and the ability to work independently. Prepare to discuss how you've balanced these aspects in previous roles. Highlight any mentoring experiences you've had, as they align with the job's requirement to coach less experienced colleagues.