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For Companies At a Glance
- Tasks: Join a dynamic team as a Sub-Investigator overseeing clinical research studies.
- Company: Be part of a leading global research services provider making a positive impact on patients' lives.
- Benefits: Flexible work options available, including part-time and full-time roles across multiple UK locations.
- Why this job: Exciting opportunity to work in innovative medicine and collaborate with top professionals in the field.
- Qualifications: Must have an MD degree, active GMC registration, and recent clinical experience.
- Other info: Equal Opportunity Employer; adjustments available for interviews.
The predicted salary is between 36000 - 60000 £ per year.
Job Description
Carrot Recruitment are acting as a recruitment agency sourcing a Clinical Trials Sub-Investigator to join a dynamic research team for multiple locations within the UK.
Winchester – Full Time
Bristol – Full Time
Birmingham – Part time or Full Time available
Due to their continued growth plans, this leading global research services provider is rapidly growing with multiple sites across the UK and US to date. It is a great opportunity to join this company at an exciting stage in its development and be part of the clinical team at a key time in their journey to positively impact patients’ lives.
The Role
The Sub-Investigator will be responsible for overseeing and implementing clinical research studies with a focus on patient safety and high-quality data collection and will work closely with the research team. Day to day the role will include bit will not be limited to the following:
- Assist in patient recruitment and screening for clinical trials
- Conduct medical assessments and provide medical oversight for clinical research studies
- Ensure strict adherence to study protocols and regulatory requirements
- Collaborate with Principal Investigators and research coordinators to ensure seamless study execution
- Provide medical expertise and guidance to research staff and study participants
- Maintain accurate and up-to-date documentation of clinical trial activities, including adverse events and protocol deviations
You
- Medical Doctor (MD) degree with active medical license (GMC registered essential)
- Recent clinical experience practising as a registered GMC doctor (essential)
- Experience in clinical research and pharmaceutical trials (desirable)
- Strong understanding of Good Clinical Practice (GCP) guidelines and regulatory standards
- Excellent communication and interpersonal skills
- Ability to work effectively in a team-oriented and fast-paced environment
- Able to provide a list of current clinical procedure competencies at point of application
What should you do next?
This role is one not to be missed; it encompasses the opportunity to work with in a highly innovative area of medicine. To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.
Unless otherwise stated, if applying for a job within the UK or European Union, you must ensure that you are already authorised to work there.
Carrot Recruitment acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.
If there are any arrangements or adjustments, we can make to assist you at interview then please let us know and we'll be more than happy to assist.
Clinical Research Physician - Sub Investigator employer: Carrot Recruitment
Contact Detail:
Carrot Recruitment Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Physician - Sub Investigator
✨Tip Number 1
Make sure to highlight your recent clinical experience and any specific roles you've had in clinical research. This will show that you have the hands-on experience needed for the Sub-Investigator position.
✨Tip Number 2
Familiarize yourself with Good Clinical Practice (GCP) guidelines and be prepared to discuss how you've applied these standards in your previous roles. This knowledge is crucial for ensuring compliance in clinical trials.
✨Tip Number 3
Network with professionals in the clinical research field, especially those who work at the company you're applying to. A referral or insight from someone within the organization can significantly boost your chances.
✨Tip Number 4
Prepare to discuss your communication and teamwork skills during the interview. The role requires collaboration with various stakeholders, so demonstrating your ability to work effectively in a team is essential.
We think you need these skills to ace Clinical Research Physician - Sub Investigator
Some tips for your application 🫡
Highlight Relevant Experience: Make sure to emphasize your recent clinical experience and any involvement in clinical research or pharmaceutical trials. This is crucial for demonstrating your suitability for the role.
Showcase Your Qualifications: Clearly state your Medical Doctor (MD) degree and active GMC registration. Include any additional certifications or training related to Good Clinical Practice (GCP) guidelines.
Detail Your Competencies: Provide a comprehensive list of your current clinical procedure competencies as requested in the job description. This will help the employer assess your qualifications effectively.
Tailor Your CV: Customize your CV to align with the specific requirements of the Sub-Investigator role. Use keywords from the job description to ensure your application stands out.
How to prepare for a job interview at Carrot Recruitment
✨Showcase Your Clinical Experience
Be prepared to discuss your recent clinical experience as a registered GMC doctor. Highlight specific cases or situations where you demonstrated your medical expertise and how it relates to the role of a Sub-Investigator.
✨Understand GCP Guidelines
Familiarize yourself with Good Clinical Practice (GCP) guidelines and regulatory standards. Be ready to explain how you have applied these principles in past research settings, as this will demonstrate your commitment to patient safety and data integrity.
✨Emphasize Team Collaboration
Since the role involves working closely with Principal Investigators and research coordinators, share examples of how you have successfully collaborated in a team-oriented environment. This will show that you can contribute effectively to the research team.
✨Prepare for Patient Interaction Scenarios
As patient recruitment and screening are key responsibilities, think of scenarios where you had to interact with patients. Discuss how you ensured their comfort and safety while adhering to study protocols, which will highlight your interpersonal skills.
