5 Research Teams jobs in London

The School has secured multi-million-pound research funding and maintains strong partnerships with UK and international universities, the NHS, charitable organisations, and industry partners. The vision is to establish the School as a world leader in healthcare engineering.

The Research Development Manager is a senior role within the School of Biomedical Engineering & Imaging Sciences, responsible for driving large-scale, high-profile healthcare engineering grants that deliver real-world patient benefits and measurable impact. Working closely with the Head of School, Heads of Research Departments, academic and research staff, and external stakeholders, this role will play a pivotal part in securing funding, fostering strategic collaborations, and facilitating the translation of healthcare engineering innovations into clinical applications.

The Research Development Manager will be instrumental in realizing the School’s vision by providing strategic and operational support, they will support the development and submission of competitive grant applications, fellowships, and funding proposals to governmental agencies, Charities, and industry sponsors. The role requires a strong scientific background, exceptional writing skills, and the ability to translate complex research concepts into clear, compelling narratives tailored to funder priorities.

This is a full time (35 Hours per week), and you will be offered an indefinite contract.

• Lead the design, synthesis, and optimization of complex organic molecules for pharmaceutical applications.
• Develop innovative and scalable synthetic routes, addressing challenges in process chemistry.
• Direct research efforts in medicinal chemistry to identify and improve lead compounds.
• Utilize advanced analytical techniques (e.g., NMR, MS, X-ray crystallography) for structural elucidation and purity assessment.
• Collaborate with cross-functional teams, including biologists, toxicologists, and formulation scientists, to advance drug candidates.
• Oversee and mentor junior research chemists, guiding their technical development and project execution.
• Develop and implement robust quality control measures for chemical synthesis and intermediates.
• Contribute to intellectual property generation through patent filings and scientific publications.
• Stay abreast of cutting-edge research, emerging technologies, and industry best practices in organic and medicinal chemistry.
• Prepare detailed scientific reports, presentations, and regulatory documentation.
• Ensure compliance with all laboratory safety regulations and ethical guidelines.
• Manage research project timelines, resources, and budgets effectively.

• Ph.D. in Organic Chemistry, Medicinal Chemistry, or a closely related field.
• Minimum of 8 years of relevant industrial experience in pharmaceutical research and development.
• Demonstrated track record of successfully leading complex synthetic chemistry projects.
• Extensive experience in modern synthetic methodologies, reaction optimization, and process development.
• Expertise in analytical characterization techniques for organic compounds.
• Strong understanding of drug discovery principles, pharmacokinetics, and toxicology.
• Proven ability to interpret complex data and provide strategic insights.
• Excellent leadership, communication, and interpersonal skills.
• Experience with computational chemistry and molecular modeling is advantageous.
• Ability to thrive in a collaborative, fast-paced, hybrid research environment.

• Lead the development and optimization of robust, scalable, and cost-effective manufacturing processes for small molecules and biologics.
• Design and execute laboratory experiments to define critical process parameters and develop comprehensive process understanding.
• Utilize advanced analytical techniques and Process Analytical Technology (PAT) to monitor and control manufacturing processes.
• Translate laboratory-scale processes to pilot and commercial-scale manufacturing, ensuring successful technology transfer.
• Collaborate closely with discovery research, formulation development, analytical development, and regulatory affairs teams.
• Ensure all process development activities comply with Good Manufacturing Practices (GMP) and relevant regulatory guidelines (FDA, EMA).
• Troubleshoot manufacturing issues and implement effective corrective and preventive actions (CAPAs).
• Develop and manage project plans, timelines, and resources for process development initiatives.
• Stay abreast of emerging technologies, scientific advancements, and industry best practices in pharmaceutical manufacturing.
• Author, review, and approve technical reports, development protocols, and regulatory submission documents.
• Mentor and guide junior scientists and engineers within the process development team.
• Contribute to the strategic direction of the R&D organization regarding manufacturing capabilities.
• Manage intellectual property and contribute to patent filings related to novel processes.
• Maintain a high level of scientific rigor and ethical conduct throughout all research activities.

• PhD in Organic Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related discipline.
• Minimum of 10 years of experience in pharmaceutical process development, with a strong emphasis on API manufacturing.
• Extensive experience in process scale-up, optimization, and validation.
• In-depth knowledge of synthetic organic chemistry, reaction kinetics, and purification techniques.
• Proven experience with GMP regulations and regulatory filing requirements (IND, NDA, BLA).
• Familiarity with Process Analytical Technology (PAT) and Quality by Design (QbD) principles.
• Strong analytical and problem-solving skills, with a meticulous attention to detail.
• Excellent leadership, communication, and project management skills.
• Ability to work independently and effectively lead cross-functional teams in a remote setting.
• Demonstrated track record of successfully bringing pharmaceutical products from development to market.
• Experience with biologics manufacturing processes is a plus.

Work From Home - Research Panelist / Focus Group (Remote)

Part-Time | Remote Work Opportunity | Flexible Schedule

About This Opportunity

We are seeking dedicated individuals to participate in legitimate market research studies as remote research panelists across the USA. This role involves completing paid surveys, participating in focus groups, and contributing to clinical research studies from the comfort of your home.

Position Overview

As a Research Panelist, you will provide valuable insights through various research methodologies including online surveys, phone interviews, and virtual focus groups. This is an excellent supplemental income opportunity that allows you to work on your own schedule while contributing to important market research initiatives.

Key Activities:

• Complete online surveys and questionnaires (5-30 minutes each)
• Participate in phone interviews and virtual focus groups
• Provide feedback on products, services, and market trends
• Maintain accurate records of participation
• Follow research protocols and guidelines

Requirements

Essential Qualifications:

• Computer or mobile device with reliable internet connection
• Quiet workspace free from distractions
• Ability to work independently with minimal supervision
• Strong reading comprehension and communication skills
• Smartphone with camera or webcam for verification purposes

Compensation & Benefits

Earning Potential:  $50 to $00 USD per month for regular participants

• Survey completion: 0.25 - 5.00 per survey
• Focus groups: 50 - 300 per session

Benefits:

• Flexible scheduling - work when convenient for you
• No commute required - 100% remote work
• Skill development in market research and data analysis
• Supplemental income opportunity
• No educational requirements or previous experience necessary

Work Environment

This is a fully remote, part-time position with flexible hours. Participants typically dedicate 1-3 hours daily to maximize earning potential. Work can be completed evenings, weekends, or during personal downtime.

Application Process

Qualified candidates will undergo a brief verification process to ensure eligibility for research studies. All personal information is kept strictly confidential in accordance with privacy regulations.

Important Note:  This position is designed as supplemental income and should not be considered full-time employment. Earnings depend on study availability and individual participation levels.