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Senior Research Physician - Glasgow 5 days a week on site Competitive salary and benefits 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) preffered, • 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) Medical Science Liaison – Scotland & Northern Ireland Pharma-Partners is exclusively recruiting for this vacancy. For this vacancy we can consider candidates at either Medical Science Liaison (MSL) or Senior MSL level and can be located in either Scotland or Northern Ireland. Working alongside a team of Senior MSLs and MSLs, this role will support a specialised portfolio of treatments that relate to a wide variety of therapy areas. The (Senior) Medical Science Liaison will focus on establishing and maintaining relationships with KOLs across the territory, support clinical development and commercialisation efforts, and acts as a scientific expert for the business. If hired as a Senior MSL the successful candidate will take on the additional responsibility as a "Therapy Area Medical Lead". This means a greater level of strategic involvement and leadership/oversight of national projects both within the Medical Affairs team and with cross functional colleagues. You therefore act as more of a hybrid MSL/Medical Advisor type role. Key Responsibilities: • Be a field medical expert for the portfolio and lead within an assigned therapy area, • Project manage national activities for a designated therapy area, • Contribute to the development of medical strategy and planning, • Engage with KOLs in scientific exchange, and develop and maintain meaningful relationships across the territory, • Share relevant insights within medical and cross-functional teams, • Support and deliver medical training of commercial field teams, • Involvement in UK clinical research activities, • Provide coaching and support to the wider field medical group, • Ensure adherence to company SOPs and the ABPI Code, • Input into cross functional plans and provide scientific expertise and advice as needed, • Represent the business and medical team at local, regional and global congress and symposia The Candidate: • Relevant Science based degree with advanced Degree level seen as desirable, • UK focused MSL experience, • Demonstrable experience in building and maintaining KOL relationships, • Knowledge of clinical trial processes and regulatory requirements, • Any therapy area background can be considered, • Experience in and knowledge of the different UK healthcare systems, • Strong team working and collaborative approach, • Effectively assimilate scientific and clinical data to the relevant audience To Apply: To apply for this position please use the “Apply” option or feel free to send your CV directly to the Pharma-Partners team via email

Medical input into the design of clinical study protocols, participant information sheets and informed consent forms, clinical trial risk assessments and clinical study reports. We are looking for a full time Pharmaceutical Physician specialising in Clinical Research to join our clinical team in BDD

We are seeking an experienced Software Tester to lead end‑to‑end transformation of our testing strategy, processes and tooling for Clinical Trial Database systems and API integrations.

A leading educational institution in Glasgow is seeking an experienced Software Tester to enhance their testing strategy for Clinical Trial Database systems. Responsibilities include supporting QA processes aligned with Agile/Scrum methodologies and ensuring adherence to clinical standards.

For many, taking part in clinical research offers hope, purpose, and a chance to shape the future of dementia care. But finding the right trial, understanding what it involves, and knowing how to take part can be confusing.

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Ensures compliance of clinical trials with national and international regulatory requirements and co‑monitors the assigned

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The Clinical Trials Manager will manage individual clinical trials and/or programs as part of the Clinical Trial Working Group. Manage monitoring activities (may include routine on-site clinical monitoring) at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs and study

A clinical trial consultancy in the United Kingdom is looking for a skilled statistical lead to oversee clinical trial programs/projects. Master’s degree in statistical science or a related field, along with demonstrated experience in clinical trial projects. You will provide statistical methodolo

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A pharmaceutical company in the United Kingdom is seeking a Clinical Trial Manager to oversee all aspects of clinical trial management for global studies, ensuring compliance with regulatory standards. The ideal candidate will have a bachelor’s degree in a related field and over 5 years of experie

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Provides guidance to clinical teams and clinical sites regarding collection, storage, and shipping of samples acquired in the course of clinical trials or other human sample acquisition projects. We are seeking a professional with working knowledge of clinical trials and clinical databases. Prior ex

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