clinical-research

EMS Healthcare is the UK’s leading supplier of mobile facilities that relieve hospital capacity and support vital clinical research.

We partner with NHS Trusts and private healthcare providers, enabling the delivery of essential patient services to communities across the country. 

Together, we reduce patient waiting times, tackle health inequalities and work closely with the NHS in delivering additional lab capacity to support life-changing research.


EMS Healthcare

• Identify, develop, and secure new business opportunities with pharmaceutical companies, biotech firms, and CROs to place clinical trials at our managed research sites.
• Build and maintain long-term relationships with key industry stakeholders, including sponsors, CROs, and investigator sites.
• Lead the negotiation of budgets, and support with negotiation of contracts, master service agreements (MSAs), and clinical trial agreements to maximise revenue and profitability.
• Maintain a strong pipeline of potential clinical trial opportunities and ensure timely follow-up to drive conversions.
• Prepare written presentations, reports and proposals, including but not limited to formal requests for quotations, bids and tenders.
• Prepare key account plans and present to the Board upon request.
• Represent the organisation at industry conferences, networking events, and client meetings to enhance visibility and credibility.
• Collaborate with cross-functional teams, including operations, finance, and regulatory, to ensure seamless trial execution and client satisfaction.
• Ensure Salesforce is utilised to its full potential, using it as your day-to-day sales management and customer management tool.
• Monitor industry trends, competitor activities, and regulatory changes to identify opportunities for business growth.
• Contribute to the development and implementation of strategic business plans and clinical research specific projects that align with company objectives.
• Provide reports on pipeline, revenue forecasts, and market insights.
• Work closely with clinical operations to ensure site readiness, feasibility assessments, and efficient study start-up processes.
• Partner with marketing to develop effective outreach campaigns and promotional materials to support business development efforts.
• Serve as a key liaison between sponsors and internal teams to address client concerns and ensure superior service delivery.

Associate Director – Clinical Research

Associate Director managing clinical research sales initiatives and driving business growth strategy. Leading relationships with pharmaceutical, biotech, and CRO partners for a clinical research site management organization.

LivaNova PLC is a global medical technology company built on nearly five decades of experience and a relentless commitment to improve the lives of patients around the world. Our advanced technologies and breakthrough treatments provide meaningful solutions for the benefit of patients, healthcare professionals and healthcare systems.

At LivaNova, we understand the importance of bringing both clinical and economic value to our customers. We are a strong, market-leading medical technology and services company, offering a diverse product portfolio and global reach. LivaNova is listed on the NASDAQ stock exchange under the ticker symbol “LIVN.” 

LivaNova has approximately 2,900 employees worldwide. We are headquartered in London (UK) and maintain a presence in more than 100 countries. 

LivaNova is a worldwide leader in cardiopulmonary and neuromodulation, dedicated to creating meaningful products and therapies that transform lives each and every day.

LivaNova

• Provide statistical support for clinical trials in medical devices under the direct supervision of a senior biostatistician.
• Conduct data analysis for clinical trial publications under supervision and collaborate with internal and external partners.
• Support and execute clinical trials activities for medical devices including: Clinical trial design and sample size calculations for Clinical Study Synopsis and Clinical Investigation Plans (protocols).
• Input on effective data collection methods.
• Statistical Analysis Plans (SAPs) with appropriate methodology and data presentation.
• Interpretation and communication of data and statistical results, including Clinical Study Report (CSR) development.
• Contribute to project management plans and meet deadlines.
• Communicate statistical concepts and results clearly to non-statistical colleagues.

Intern – Biostatistician

Intern providing statistical support for clinical trials in medical devices under supervision. Conduct data analysis, support clinical trials activities, and communicate statistical results clearly.

Amicus Therapeutics is a biotechnology company at the forefront of advanced therapies to treat a range of devastating rare diseases. The company focuses on developing innovative treatments for human genetic diseases, with a pipeline that includes therapies for conditions like Fabry Disease and Pompe Disease.

We are a global, patient-dedicated biotechnology company focused on discovering, developing, and delivering high-quality medicines for people living with rare metabolic diseases. 

Amicus is the Latin word for friend. This name signifies our collaborative approach to developing medicines by incorporating the patient perspective every step of the way. Our company was founded by an entrepreneur who embarked on a life-long journey to transform the lives of those living with devastating conditions when two of his children were diagnosed with a rare disease. That spirit of empathy, compassion, and tenacity permeates our culture and influences all aspects of our approach to advancing cutting-edge technologies.

Building on our core beliefs, our mission-focused behaviors help us define and shape our culture; drive performance and innovation; inform development and growth; and attract, energize, and retain the right talent. By championing mission-dedication, innovation, performance, and integrity, we are united by our passion for making a difference and committed to pushing ideas as far and as fast as possible.

Our global footprint spans over 20 countries, including our global headquarters in Princeton, NJ and international headquarters in Marlow, UK. Additional international office locations include Australia, Canada, France, Japan, Germany, Italy, The Netherlands, and Spain. More information about Amicus and our career opportunities can be found at www.amicusrx.com.

Amicus Therapeutics

• Lead the pharmacovigilance and drug safety strategy for investigational and marketed products• Establish and maintain a comprehensive safety surveillance system to detect, assess, and report adverse events• Ensure compliance with global regulatory requirements (FDA, EMA, etc.) and guidelines (ICH, GCP) related to clinical safety• Provide safety assessments for clinical development, risk management plans, and post-marketing surveillance• Serve as the primary contact for regulatory authorities on safety issues and risk management strategies• Support GVP audit and inspection preparedness• Build, mentor, and lead high-performing teams in drug safety• Foster a collaborative environment that encourages innovative thinking and best practices• Partner with senior leadership to drive organizational growth and support company-wide strategic initiatives• Represent the company at key scientific, regulatory, and industry events to enhance external visibility and partnerships• Ensure safety activities are conducted in full compliance with local and international regulations• Collaborate with regulatory affairs on submissions, safety reports, and labeling for both investigational and commercial products• Maintain up-to-date knowledge of regulatory changes, industry trends, and scientific advancements affecting drug safety and clinical development• Provide expert clinical and safety risk assessments to support product development, regulatory filings, and commercial activities• Implement risk mitigation strategies for safety concerns that arise during clinical trials or post-approval• Critical leadership role in company governance forums related to safety, labeling, and clinical development strategy• Work closely with internal stakeholders to make informed, data-driven decisions on the progression of clinical programs• Support business development teams by providing safety expertise during the evaluation of potential in-licensing, co-development, or acquisition opportunities• Conduct in-depth due diligence on new assets, including assessing safety profiles, and evaluating regulatory pathways• Collaborate with internal teams and external partners to identify potential risks and opportunities associated with new assets

Vice President of Clinical Research – Global Drug Safety

Vice President of Global Drug Safety at Amicus Therapeutics focusing on rare metabolic diseases and ensuring safety compliance. Driving innovation and high standards in pharmacovigilance and risk management.

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.

We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

ICON plc

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Clinical Trial Manager – Biotech

Clinical Trial Manager overseeing planning and execution of clinical trials at ICON plc. Driving successful delivery of clinical trial outcomes with cross-functional team collaborations.

• Serves as lead biostatistician for programs of studies, submissions, or on simple to complex individual studies.
• Oversees statistical activities that support ICON’s interactions with clients and regulatory agencies.
• Reviews and approves statistical methods sections of study protocols, statistical analysis plans and statistical input to reports.
• Prepares and approves research proposals and budgets to provide statistical consulting and to conduct statistical analyses for clients.
• Participates in bid defense meetings and makes presentations at marketing meetings with prospective clients.

Principal Biostatistician

Principal Biostatistician managing clinical trials and statistical analyses for ICON plc. Lead biostatistical efforts in drug development across multiple sponsors focusing on Vaccines, Oncology, and Rare Diseases.

Hybrid Clinical Researchers roles in United Kingdom

Browse 5 hybrid clinical researchers roles hiring in United Kingdom plus related opportunities such as medical writer, biostatistician, data scientist, clinical operations, medical director and medical reviewer.

5 jobs found

Associate Director – Clinical Research

EMS Healthcare

Intern – Biostatistician

LivaNova

Vice President of Clinical Research – Global Drug Safety

Amicus Therapeutics

Clinical Trial Manager – Biotech

ICON plc

Principal Biostatistician

ICON plc