125 Pharmaceutical Development jobs in the United Kingdom
Learning and Development Business Partner Global Pharmaceutical
Posted 1 day ago
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Job Description
Crone Corkill
Recruiting on behalf of a global pharmaceutical company –
Seeking a L&D Professional ideally experienced within the area of Market Access Launches
Project life cycle management pre, post launch
Working with global stakeholders across L&D , technical and Market Access
The design and development of the learning projects, as they bring them to pilot phase
- Conducting Global Learning needs assessments
Pulling through launch plans and working with markets on post launch milestones, analysis and continued static and diagnostic learning interventions.
- Proactively gathering insights into the stakeholder needs and helping them to identify how and whether learning and development can best support these
- Works with the global Learning team in developing specific projects by contributing with therapeutic and expertise knowledge towards:
- Work closely with key stakeholders across patient Impact, patients evidence and Assets teams to partner whilst using your own knowledge and act as SMEs in the learning experience.
- Coordinates the smooth implementation of the learning experiences – input on planning, briefing or train-the-trainer of potential facilitator team, troubleshooting, issue management
- Together with the Learning team, work on iterations of learning experience according to insights gathered; Innovate and explore digital opportunity to further develop Learning Solutions
Director Formulation & Process Development
Posted 5 days ago
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Job Description
We are currently looking for a Director Inhaled Formulation & Process Development to join a leading pharmaceutical company based in South East, England. As the Director Inhaled Formulation & Process Development, you will be responsible for leading the development of new respiratory products, ensuring technical excellence and innovation.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Director Inhaled Formulation & Process Development will be varied however the key duties and responsibilities are as follows:
1. Lead the delivery of project activities to take new respiratory products to clinical studies and commercialisation.
2. Support the planning and execution of experiments to generate scientific understanding in the development of analytical methods, formulations, and/or manufacturing processes.
3. Ensure the smooth transfer of analytical methodologies or manufacturing processes to commercial facilities.
4. Lead the review and/or approval of data, interpretation of results, and reporting of experimental outcomes to project development teams.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Director Inhaled Formulation & Process Development we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific field such as Chemistry, Analytical Chemistry, Chemical Engineering, Pharmacy, or Pharmaceutical Sciences.
2. Substantial industry experience in pharmaceutical product development, particularly in the development of inhalation products.
3. A working knowledge and practical experience with the challenges involved in the validation and transfer of complex analytical methods or manufacturing processes to commercial facilities.
Key Words:
Director / Inhaled Formulation / Process Development / Pharmaceutical / Respiratory Products / Analytical Methods / Manufacturing Processes / Clinical Studies / Product Development / Regulatory Submissions
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Director Formulation & Process Development
Posted 8 days ago
Job Viewed
Job Description
We are currently looking for a Director Inhaled Formulation & Process Development to join a leading pharmaceutical company based in South East, England. As the Director Inhaled Formulation & Process Development, you will be responsible for leading the development of new respiratory products, ensuring technical excellence and innovation.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Director Inhaled Formulation & Process Development will be varied however the key duties and responsibilities are as follows:
1. Lead the delivery of project activities to take new respiratory products to clinical studies and commercialisation.
2. Support the planning and execution of experiments to generate scientific understanding in the development of analytical methods, formulations, and/or manufacturing processes.
3. Ensure the smooth transfer of analytical methodologies or manufacturing processes to commercial facilities.
4. Lead the review and/or approval of data, interpretation of results, and reporting of experimental outcomes to project development teams.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Director Inhaled Formulation & Process Development we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific field such as Chemistry, Analytical Chemistry, Chemical Engineering, Pharmacy, or Pharmaceutical Sciences.
2. Substantial industry experience in pharmaceutical product development, particularly in the development of inhalation products.
3. A working knowledge and practical experience with the challenges involved in the validation and transfer of complex analytical methods or manufacturing processes to commercial facilities.
Key Words:
Director / Inhaled Formulation / Process Development / Pharmaceutical / Respiratory Products / Analytical Methods / Manufacturing Processes / Clinical Studies / Product Development / Regulatory Submissions
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Clinical Research Coordinator
Posted 5 days ago
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Job Description
Job Title: Clinical Research Coordinator (Band 6 Nurse)
Contract Type: Part-Time (2–3 days/week)
Overview:
We are seeking a skilled and motivated Band 6 Nurse to support clinical research activities as a Clinical Research Coordinator. This part-time role offers an excellent opportunity to contribute to impactful research while maintaining a flexible schedule.
Key Responsibilities:
- Identify and recruit eligible patients for clinical trials.
- Perform accurate and timely data entry into study databases.
- Collaborate with research and clinical teams to ensure protocol compliance.
- Maintain high standards of documentation and regulatory adherence.
Requirements:
- Registered Band 6 Nurse with relevant clinical experience.
- Demonstrated experience in patient identification and data entry.
- Strong attention to detail and organizational skills.
- Must be available to work every Wednesday, plus two additional weekdays.
Please submit your CV or get in touch via email:
Clinical Research Physician
Posted 12 days ago
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Job Description
Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
Clinical Research Physician
Posted 12 days ago
Job Viewed
Job Description
Our client, an innovative clinical research organisation (CRO) is currently looking for a Clinical Research Physician to join their team in London.
As a Clinical Research Physician, you will spearhead early stage clinical trials, manage study protocols and ensure ethical conduct and compliance at all stages. You will collaborate with an expert sponsor team and contribute to ground-breaking projects that advance healthcare and improve patient outcomes.
You will be driven to enhance patient safety, improve quality systems and ensure the data produced for the development of individual drugs is of the highest standard.
This role will offer tremendous scope for leadership and personal development. With this site being relatively new, this person will have the remit to grow and nurture a clinical research team around them as well as having significant involvement and influence with their sponsors.
Key Responsibilities
- Provide medical direction, oversee protocol compliance and ensure participant safety throughout clinical trials.
- Evaluate and interpret clinical data, performing necessary assessments to maintain data accuracy and integrity.
- Collaborate on scientific feasibility for new inquiries, assisting sponsors and guiding clinical operations teams as needed.
- Ensure adherence to regulatory requirements and Good Clinical Practice standards, maintaining rigorous documentation and participant confidentiality.
Requirements
- A medical degree (MD) - essential
- Full and current GMC registration - essential.
- Strong background in clinical research / clinical trials.
- Proven experience as a Clinical Research Physician.
- Strong knowledge of regulatory guidelines.
- Excellent organisational, communication and analytical skills.
Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Agency in relation to this role.
Clinical Research Physician
Posted 15 days ago
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Job Description
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Clinical Research Physician
Posted 15 days ago
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Job Description
Job Title: Clinical Research Physician
Location: Liverpool, UK
Employment Type: Full-time
Reports To: Medical Director / Principal Investigator / Site Director
About the Role:
We are seeking a motivated and experienced Clinical Research Physician to join our dynamic clinical trials network in Liverpool . This is a patient-facing role where you will act as a Sub-Investigator or Principal Investigator across a range of Phase I–IV clinical studies in collaboration with global sponsors and CROs. You will play a pivotal role in delivering high-quality clinical research within a network of well-established trial sites.
Key Responsibilities:
- Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) on assigned clinical trials.
- Provide medical oversight and ensure participant safety throughout the study lifecycle.
- Conduct study-related procedures including medical assessments, physical examinations, and AE/SAE evaluations.
- Review and assess eligibility criteria, informed consent documentation, and patient medical histories.
- Liaise with study sponsors, monitors (CRAs), ethics committees, and regulatory authorities as needed.
- Ensure GCP compliance and adherence to protocol, SOPs, and applicable regulations.
- Contribute to site feasibility, study start-up, and recruitment planning activities.
- Support medical input into recruitment materials and protocol reviews.
- Maintain accurate documentation in accordance with regulatory and sponsor expectations.
- Provide clinical leadership and guidance to site staff including nurses, coordinators, and administrative teams.
Essential Qualifications and Experience:
- Medical degree (MBBS, MBChB or equivalent) and full GMC registration .
- Minimum 1–2 years of experience in clinical research or clinical trials (preferably Phase II–IV).
- Knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent clinical judgment and ability to make sound medical decisions.
- Strong communication and interpersonal skills.
- Ability to work effectively within a multidisciplinary team.
Desirable:
- Experience acting as PI or Sub-I in commercial clinical trials.
- Background in general medicine, internal medicine, or a therapeutic area relevant to trials (e.g., vaccines, cardiology, respiratory, CNS).
- Interest in expanding research expertise and participating in multiple therapeutic areas.
- ALS/BLS certification (training can be provided).
Clinical Research Associate
Posted 1 day ago
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Job Description
Are you a passionate CRA II or Senior CRA looking for your next challenge?
We have an exciting, exclusive opportunity for an experienced Clinical Research Associate to join our clients newly established FSP team, working exclusively with a leading Pharmaceutical client.
This is a unique opportunity to be part of a dynamic and supportive environment where your contributions directly impact the future of medicine. Our clients FSP model provides the stability and support of a dedicated team, while you gain exposure to the innovative research of a top-tier pharmaceutical company.
About the role:
As a CRA II or Senior CRA, you will be responsible for the full range of monitoring activities, from site initiation to close-out. You'll ensure the highest standards of data quality and compliance with ICH-GCP, protocols, and all applicable regulations. This role is home-based and will involve travel to sites across your designated region.
What our client offer:
- Salary: £45,000 - £55,000 per annum, depending on experience.
- Car/Car Allowance: A company car or a competitive car allowance.
- Bonus & Benefits: An attractive bonus scheme and a comprehensive benefits package.
- Career Growth: We are committed to your professional development and offer extensive training, mentorship, and opportunities for progression within our growing FSP.
Location:
This is a home-based role to be based in one of the following regions:
- North England
- North West England
- Midlands
- London
- South England
Requirements:
- Proven experience as a CRA, with a strong understanding of the clinical trial lifecycle. 18 months minimum as a CRA to be CRAII and 3 year + to be considered for Senior CRA.
- Excellent knowledge of ICH-GCP guidelines and relevant regulations.
- Strong communication and interpersonal skills.
- A proactive and independent approach to your work.
- A full UK driving licence and willingness to travel.
If you are ready to take the next step in your career and join a company that values growth, training, and support, we want to hear from you.
Apply now or message us for more details!
#CRA #ClinicalResearch #ClinicalResearchAssociate #SeniorCRA #CRAJobs #PharmaJobs #FSP #LifeSciences #Hiring #ClinicalTrials #UKJobs#CCS-Global
Clinical Research Physician
Posted 1 day ago
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Job Description
Urgent Nursing Opportunity
The Client
The company have had 18% over the past 2 years and are using this to further fuel their mission of connecting patients to clinical trials through their recruitment and retention activities. Founded by industry experts, they are using digital technologies to improve the reach and accessibility of clinical trials.
The Role
The role we have is for a Research Physician to support their ongoing clinical trial work dedicated to one of their site in either York or Preston.
Requirements
Minimum 4 years of experience in the NHS (Registrar level) - Making independent decisions on the ward, running outpatients clinics.
- GMC registered
About Planet Pharma:
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.