At a Glance
- Tasks: Lead clinical trials and ensure participant safety while driving high-quality research outcomes.
- Company: Join a forward-thinking clinical research organisation in Glasgow.
- Benefits: Competitive salary, comprehensive benefits, and opportunities for professional growth.
- Other info: Collaborative environment with flexibility across sites and working patterns.
- Why this job: Make a real impact in patient-centred research and clinical excellence.
- Qualifications: GMC registered physician with 5+ years of clinical experience and strong leadership skills.
The predicted salary is between 60000 - 80000 £ per year.
Pharma-Partners is supporting a growing clinical research organisation seeking to appoint a Senior Research Physician to execute and lead clinical trial delivery at its Glasgow research site. This is a key role for an experienced physician who is passionate about patient-centred research, clinical excellence, and driving high-quality study outcomes in line with regulatory and ethical standards.
The successful candidate will act as Sub Investigator or Principal Investigator (PI) on clinical trials and will play a central role in ensuring participant safety, protocol compliance, and overall study oversight. This opportunity offers the chance to contribute to cutting-edge clinical research within a forward-thinking and collaborative organisation.
Responsibilities:
- Act as Sub/Principal Investigator with overall responsibility for the conduct of clinical studies at site.
- Ensure all trials are conducted in accordance with study protocols, ICH-GCP, SOPs/COPs, and all applicable local regulations.
- Oversee and ensure appropriate training, delegation, and competency assessment of all site staff.
- Perform regular PI oversight (minimum weekly) to ensure data quality, patient safety, and protocol compliance.
- Ensure accurate, timely, and complete documentation, responding to queries within agreed timelines.
- Recruit eligible participants and ensure their ongoing wellbeing, including referrals to GPs or third parties where appropriate.
- Ensure timely reporting of Adverse Events and Serious Adverse Events in line with regulatory requirements.
- Maintain up-to-date training portfolios and complete competency assessments every three months.
- Hold regular meetings with CRAs and act on feedback to maintain high site performance standards.
- Participate in internal audits, external audits, and regulatory inspections.
- Participate in the out-of-hours/on-call rota as required.
- Support flexibility across sites and working patterns where business needs require.
Requirements:
- GMC registered physician with a licence to practise in the UK.
- MRCP (UK) preferred.
- Minimum of 5 years' clinical experience, including at least 2 years within the NHS.
- GCP trained (desirable).
- Previous experience as a Sub-Investigator or Principal Investigator in clinical trials (desirable).
- Strong leadership, communication, and organisational skills.
- Proactive, collaborative, and patient-focused approach.
Pharma-Partners and its clients are equal opportunity employers and welcome applications from all suitably qualified individuals. Applicants must have the right to work in the UK.
To apply for this position, please use the Apply option or contact the Pharma-Partners team directly for a confidential discussion.
Senior Project Physician in Paisley employer: Pharma Partners Recruitment Ltd
Pharma-Partners is an exceptional employer, offering a dynamic work environment in Glasgow where clinical excellence and patient-centred research are at the forefront. With a commitment to employee growth, competitive salaries, and comprehensive benefits, the company fosters a collaborative culture that empowers its staff to lead innovative clinical trials while ensuring participant safety and protocol compliance. Join us to be part of a forward-thinking organisation dedicated to making a meaningful impact in the field of clinical research.
Contact Details:
Pharma Partners Recruitment Ltd Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land Senior Project Physician in Paisley
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who might know about opportunities at Pharma-Partners. A personal recommendation can make all the difference!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and the latest trends in patient-centred research. We want you to shine when discussing how you can contribute to high-quality study outcomes.
✨Tip Number 3
Showcase your leadership skills! Be ready to discuss your experience overseeing clinical trials and how you've ensured participant safety and protocol compliance. We love candidates who can demonstrate their proactive approach.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you're serious about joining a forward-thinking organisation like Pharma-Partners.
We think you need these skills to ace Senior Project Physician in Paisley
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that align with the Senior Research Physician role. Highlight your clinical trial experience and any leadership roles you've held, as this will show us you're a great fit for the position.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to express your passion for patient-centred research and how your background makes you the ideal candidate. Be sure to mention your understanding of regulatory standards and your commitment to clinical excellence.
Showcase Your Achievements:When detailing your experience, focus on specific achievements rather than just listing duties. For example, if you improved patient safety or enhanced study outcomes, let us know! Numbers and results can really make your application stand out.
Apply Through Our Website:We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it shows us you’re proactive and keen to join our team!
How to prepare for a job interview at Pharma Partners Recruitment Ltd
✨Know Your Stuff
Make sure you brush up on the latest clinical trial regulations and guidelines, especially ICH-GCP. Being able to discuss these confidently will show that you're not just familiar with the basics but are also committed to maintaining high standards in patient safety and protocol compliance.
✨Showcase Your Experience
Prepare specific examples from your past roles where you've acted as a Sub-Investigator or Principal Investigator. Highlight your leadership skills and how you've ensured data quality and participant wellbeing. This will help demonstrate your hands-on experience and suitability for the role.
✨Ask Smart Questions
Come prepared with insightful questions about the organisation's approach to clinical trials and how they ensure participant safety. This shows your genuine interest in their work and helps you assess if their values align with yours.
✨Be Collaborative
Emphasise your ability to work well with others, especially when it comes to training and overseeing site staff. Share examples of how you've fostered a collaborative environment in previous roles, as this is crucial for maintaining high performance standards in clinical research.
