37 Pharma jobs in the United Kingdom

Data Engineer - AI/ML | Leading Pharma | London (Hybrid)

My client a leading pharmaceutical company is looking for a Data Engineer who thrives on solving complex challenges and building scalable data solutions that power scientific innovation.

Key Responsibilities

• Build and maintain data pipelines using Python, Spark, SQL, BigQuery , and Google Cloud
• Collaborate with scientists to meet research data needs
• Ensure high-quality, well-documented, and tested code
• Improve performance metrics and integrate data across teams

Requirements

Essential:

• Experience in data engineering
• Strong Python & SQL skills
• Experience with Google Cloud or similar
• Familiarity with unit testing , Git , and Agile

Desirable:

• Experience with bioinformatics or scientific datasets
• Knowledge of Nextflow , Airflow , NLP , and Docker
• Exposure to AI/ML applications

If the role aligns with your skills and experience, please apply with your updated CV

Business Development (Medical Devices/Healthcare)

London

Full time & permanent position

Excellent salary and benefits

Reed Scientific are working with a dynamic medical device company producing revolutionary products within the pharmaceutical industry. They are currently looking for a commercially awareness scientist with a strong background within the pharmaceutical or medical device industry to support with future business development to allow their business to expand further into international markets.

Duties of the role:

• Identifying new business opportunities and market users of specific medical device being manufactured
• Keeping up to date with changes in the market and trends and competitor activity
• Initiating and maintaining contact with potential customers
• Providing key product information to potential customers to manage customers needs and expectations
• Conducting market analysis and gathering market intelligence to identify gaps in the market and new business opportunities

Skills & experience required:

Essential:

• BSc/MSc in a scientific discipline relating Pharmaceutical Sciences or Medical Devices
• Previous experience working within a medical device, pharmaceutical company within a commercial role
• Excellent written and investigative skills, particularly using AI tools such as CoPilot

Additional:

• Commerical experience involving client development, customer/technical support and account management
• Highly motivated and target-driven
• Excellent communication skills with the ability to speak with key decision makers
• Ability to travel

If you possess the required skills and experience then please do not hesitate to get in touch or apply for the position through the link. Unfortunately, your application will not be considered if you do not have a scientific qualification and experience within a commercial role within the scientific industry.

Qualitative Research Manager, Associate Director, Director – Pharmaceutical / Healthcare. London/Hybrid £50-100k

Our client is an established market agency with a team of dynamic, award-winning and passionate experts, delivering scientifically-grounded, powerful insights to pharmaceutical and healthcare clients.

They are market research practitioners in the healthcare and pharmaceutical space and they have a wealth of experience in a wide range of therapy areas.

They are looking to add to their successful team and are interested in talking to RM-Director level qualitative candidates.

Key Accountabilities

• You will have strong involvement in managing projects and project teams and delighting your clients
• You will have the confidence, pharmaceutical sector and agency sector knowledge to be able to provide thoughtful and strategic insights to your clients through project delivery and writing engaging proposals, as well as using business development skills to build lasting client relationships

 Core competencies

 Strong Qualitative skills – any Quantitative Insight skills are a bonus

• Excellent communication and interpersonal skills (both verbal and written)
• Excellent organisational skills including ability to manage time and prioritise effectively
• Strong IT skills, skilled in using Microsoft Word, Excel packages and Powerpoint packages
• Able to work efficiently, independently and on own initiative within specified guidelines and processes
• Able to work appropriately with confidential and sensitive information
• Excellent attention to detail

You must be able to work in their London office at least once a week and have the Right To Work in the UK

Please get in touch with Tanya for more info!

#pharmaceutical #researchmanager #associatedirector #director #qualitative

Business Development (Medical Devices/Healthcare)

London

Full time & permanent position

Excellent salary and benefits

Reed Scientific are working with a dynamic medical device company producing revolutionary products within the pharmaceutical industry. They are currently looking for a commercially awareness scientist with a strong background within the pharmaceutical or medical device industry to support with future business development to allow their business to expand further into international markets.

Duties of the role:

• Identifying new business opportunities and market users of specific medical device being manufactured
• Keeping up to date with changes in the market and trends and competitor activity
• Initiating and maintaining contact with potential customers
• Providing key product information to potential customers to manage customers needs and expectations
• Conducting market analysis and gathering market intelligence to identify gaps in the market and new business opportunities

Skills & experience required:

Essential:

• BSc/MSc in a scientific discipline relating Pharmaceutical Sciences or Medical Devices
• Previous experience working within a medical device, pharmaceutical company within a commercial role
• Excellent written and investigative skills, particularly using AI tools such as CoPilot

Additional:

• Commerical experience involving client development, customer/technical support and account management
• Highly motivated and target-driven
• Excellent communication skills with the ability to speak with key decision makers
• Ability to travel

If you possess the required skills and experience then please do not hesitate to get in touch or apply for the position through the link. Unfortunately, your application will not be considered if you do not have a scientific qualification and experience within a commercial role within the scientific industry.

Qualitative Research Manager, Associate Director, Director – Pharmaceutical / Healthcare. London/Hybrid £50-100k

Our client is an established market agency with a team of dynamic, award-winning and passionate experts, delivering scientifically-grounded, powerful insights to pharmaceutical and healthcare clients.

They are market research practitioners in the healthcare and pharmaceutical space and they have a wealth of experience in a wide range of therapy areas.

They are looking to add to their successful team and are interested in talking to RM-Director level qualitative candidates.

Key Accountabilities

• You will have strong involvement in managing projects and project teams and delighting your clients
• You will have the confidence, pharmaceutical sector and agency sector knowledge to be able to provide thoughtful and strategic insights to your clients through project delivery and writing engaging proposals, as well as using business development skills to build lasting client relationships

 Core competencies

 Strong Qualitative skills – any Quantitative Insight skills are a bonus

• Excellent communication and interpersonal skills (both verbal and written)
• Excellent organisational skills including ability to manage time and prioritise effectively
• Strong IT skills, skilled in using Microsoft Word, Excel packages and Powerpoint packages
• Able to work efficiently, independently and on own initiative within specified guidelines and processes
• Able to work appropriately with confidential and sensitive information
• Excellent attention to detail

You must be able to work in their London office at least once a week and have the Right To Work in the UK

Please get in touch with Tanya for more info!

#pharmaceutical #researchmanager #associatedirector #director #qualitative

• Lead the planning, execution, and close-out of clinical trial projects.
• Develop and manage clinical study timelines, budgets, and resources.
• Oversee and manage clinical research associates (CRAs) and study site activities.
• Select, manage, and evaluate performance of CROs and other vendors.
• Ensure compliance with ICH-GCP, SOPs, and regulatory requirements.
• Develop and implement risk management plans for clinical studies.
• Liaise with regulatory authorities, ethics committees, and study sites.
• Collaborate with internal departments including R&D, regulatory affairs, and data management.
• Prepare and present study progress reports to senior management and stakeholders.
• Contribute to the development of clinical trial protocols and other study documents.

• Bachelor's or Master's degree in Life Sciences, Nursing, or related field.
• Minimum of 7 years of experience in clinical project management within the pharmaceutical or biotech industry.
• Proven experience managing Phase I-IV clinical trials.
• In-depth knowledge of ICH-GCP, regulatory guidelines, and clinical trial processes.
• Strong vendor management and negotiation skills.
• Excellent leadership, communication, and interpersonal abilities.
• Proficiency in project management software and clinical trial management systems (CTMS).
• Demonstrated ability to manage budgets and timelines effectively.
• Strong problem-solving and risk-management skills.
• Ability to work independently and effectively in a remote team environment.

• Conduct pre-study, initiation, routine monitoring, and close-out visits to clinical trial sites.
• Ensure adherence to study protocols, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
• Verify the accuracy, completeness, and integrity of clinical data through source data verification (SDV).
• Manage and motivate study site staff, providing training and ongoing support.
• Oversee patient recruitment and retention efforts at trial sites.
• Ensure timely reporting of study progress, safety issues, and any deviations from protocol.
• Maintain accurate and organised trial master files (TMF) and other essential documentation.
• Liaise with investigators, study coordinators, and other site personnel to resolve study-related issues.
• Prepare monitoring visit reports and follow up on action items.
• Ensure compliance with regulatory requirements and company policies.
• Contribute to the identification and selection of suitable clinical trial sites.

• A Bachelor's degree in a life science, nursing, or a related discipline.
• Minimum of 2-3 years of experience as a Clinical Research Associate, preferably within the pharmaceutical industry.
• Strong understanding of GCP, ICH guidelines, and regulatory requirements for clinical trials.
• Proven experience in monitoring clinical trials and conducting SDV.
• Excellent organisational, time management, and problem-solving skills.
• Exceptional written and verbal communication skills.
• Ability to travel frequently to clinical sites (up to 60-70% travel expected).
• Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• A proactive approach and the ability to work independently with minimal supervision.
• Commitment to maintaining high standards of data quality and patient safety.

• Perform site selection, initiation, monitoring, and close-out visits at clinical trial sites.
• Verify the accuracy and completeness of clinical trial data through source data verification (SDV).
• Ensure compliance with the study protocol, regulatory requirements (e.g., FDA, EMA), and GCP guidelines.
• Train and support investigators and site staff on study-related procedures and data collection.
• Manage site communications, resolving issues and escalating as necessary.
• Oversee the investigational product management and accountability at clinical sites.
• Review and ensure the timely submission of essential regulatory documents.
• Prepare monitoring reports and follow up on action items with study sites.
• Ensure the safety and well-being of trial participants by closely monitoring adverse events and reporting requirements.
• Collaborate with project managers, data managers, and other members of the clinical operations team.
• Maintain effective working relationships with investigators, site staff, and internal stakeholders.
• Contribute to the development and revision of clinical trial protocols and other study documents.

• A Bachelor's degree in a life science, nursing, pharmacy, or a related field. A Master's degree or higher is advantageous.
• Minimum of 2-3 years of independent clinical monitoring experience as a CRA.
• Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
• Demonstrated experience in SDV and excellent attention to detail.
• Strong therapeutic area knowledge is a plus.
• Excellent communication, interpersonal, and negotiation skills.
• Ability to manage multiple priorities and work effectively under pressure.
• Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
• Willingness to travel extensively to clinical sites within the assigned territory.
• Strong analytical and problem-solving abilities.

• Develop and implement regulatory strategies for new and existing pharmaceutical products.
• Prepare, review, and submit regulatory dossiers (e.g., CTD, IND, NDA, MAA) to health authorities worldwide.
• Act as the primary point of contact with regulatory agencies, responding to queries and managing meetings.
• Monitor and interpret changes in the regulatory landscape, providing proactive guidance to project teams.
• Assess the regulatory impact of product changes and manufacturing processes.
• Collaborate with R&D, Quality Assurance, Clinical Affairs, and Commercial teams to ensure alignment on regulatory requirements.
• Review promotional materials and labelling for regulatory compliance.
• Manage post-approval regulatory activities, including variations, renewals, and annual reports.
• Contribute to the development and maintenance of regulatory SOPs and quality systems.
• Identify potential regulatory risks and propose mitigation strategies.

• Bachelor's or Master's degree in Pharmacy, Life Sciences, Chemistry, or a related field.
• Minimum of 5-7 years of progressive experience in pharmaceutical regulatory affairs.
• In-depth knowledge of global regulatory requirements for pharmaceuticals (e.g., FDA, EMA, MHRA).
• Proven experience in preparing and submitting regulatory dossiers for various product types.
• Excellent understanding of drug development processes and GMP/ICH guidelines.
• Strong scientific writing, analytical, and problem-solving skills.
• Exceptional communication, interpersonal, and negotiation skills.
• Ability to manage multiple projects simultaneously and meet tight deadlines.
• Proficiency in regulatory information management systems is a plus.
• Must be able to work independently and as part of a distributed team.