Clinical trial jobs in OxfordCreate job alerts

The Strategic Development Manager will work closely with Country Management to support the development and expansion of UK & Ireland operations and assist in the set up of Milestone One. Some of the activities conducted by the SDM include; • Communication of recommendations for development of operational strategy including identification of optimal site profile and enrollment rates., • Identification of potential clinical trial sites and evaluation of their capabilities infrastructure and staff qualifications., • Development and maintenance of a database of potential and active sites for PSI critical therapeutic areas., • Development of outreach plans to engage potential sites in under-developed or strategic regions., • Monitoring of market trends emerging therapeutic areas and competitor activities to identify business opportunities in the country/region., • Establishment and maintenance of relationships with key stakeholders including site investigators site staff and healthcare administrators., • Assessment of patient enrollment challenges and opportunities in ongoing and completed studies to improve patient recruitment and retention strategies., • Analysis of patient enrollment upon completion and comparison of the feasibility assessment against actual performance to determine future improvement opportunities., • Collection of feedback from PSI Operations to support feasibility and site identification., • Participation in scientific conferences meetings symposia etc. to collect information network with potential sites/investigators and obtain in-depth understanding of clinical trials setting in the country/region. Qualifications : • Life Science Degree and/or equivalent experience, • At least 5 years of on-site experience in clinical research, • Experience in clinical site identification is a plus, • Proficiency in standard MS Office applications Additional Information : If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people then PSI is the right choice for you. Remote Work : Yes Employment Type : Full-time Key Skills Bidding,Crane,Finance Management,Accountancy,Avionics,Blackberry Experience: years Vacancy: 1

Life Sciences Lawyer, 5+ PQE, Oxfordshire, Salary up to £80-110,000 (DOE) – An outstanding opportunity to develop your career with an award winning, top 50, UK Law firm, with excellent salary and benefits package on offer. For more information or to apply for this role contact Gemma on 020 7183 8586. TITLE: Life Sciences Lawyer PQE: 5+ LOCATION: Oxfordshire SALARY: £80-110,000 (DOE) THE ROLE: This highly regarded firm is looking for a senior solicitor to join its specialist Life Sciences team to provide advice to a broad range of commercial clients and academic, medical, and governmental institutions. The role will involve working closely with the head of department to advise on clinical trial arrangements, IP licensing and protection, partnering transactions, research collaborations, promotional arrangements, regulatory issues within the life sciences sector, data protection, commercial contracts, and due diligence for corporate and commercial transactions. THE CANDIDATE: The successful candidate will have a minimum of 5 years’ PQE gained from a leading law firm or in-house environment, with a strong background in life sciences, solid technical expertise, and a commercially minded approach. You should have excellent interpersonal skills, the ability to build strong client relationships, and the capability to collaborate effectively with both the team and other departments. THE FIRM: This is an excellent opportunity to join a specialist team in the Oxford office of this highly regarded top UK 50 firm. You will advise a diverse range of life sciences clients and other tech-based clients, working on high-quality matters alongside a team of dedicated professionals committed to fostering a supportive environment and delivering outstanding results. THE PACKAGE: An excellent salary and benefits package is on offer, including staff bonuses, a generous pension scheme, five weeks’ annual leave, enhanced maternity / paternity leave and pay, income protection (after 2 years’ service), life assurance, and employee assistance programme. TO APPLY: Contact Gemma Jones at eNL on 020 7183 8586 or email with your CV or simply call for a confidential discussion. eNL will never share your CV with a third party without your express permission. As part of our candidate care process, we aim to respond to all applications in 7 days. If you have not been contacted within this timescale, your application has been unsuccessful on this occasion. Please note our advertisements use PQE/salary levels purely as a guide. At eNL we value diversity and inclusion. We want to attract people at all levels and encourage applications from all suitably qualified candidates, whatever your ethnicity, religion, age, physical or mental disability, sexual orientation, gender identity or any characteristics protected by law in the jurisdictions in which we operate.

As a Clinical Trial Manager you will take overall responsibility for the day-to-day management of multi-centre randomised clinical trials. You will also oversee trial data collection and perform regular systematic checks of information held on trial database as required and you will act as a resourc

PE Global is currently recruiting for a Senior Clinical Genetics Lead for a leading multi-national Biotech client. Experience independently leading research projects, particularly those using clinical trial data or other regulated setting,. Senior Clinical Genetics Lead, oxford district.

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

Social network you want to login/join with:.Associate Director, AI Data Scientist - Mid-sized pharmaceutical company - Fully remote across UK, oxford district.Associate Director, AI Data Scientist.AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare.This is a hig

I am privileged to manage and support our fantastic technical team of Pharmacy Technicians, Science Manufacturing Technicians , Clinical Trial Practitioners , Assistants and Apprentices as we provide support services to clinical trial research teams on all our Trust sites throughout Oxfordshire. To

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. The manager is responsible for all performance metrics and quality of deliverables in the clinical trial. Oversees maintenan

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

As a Project Administrator, you will be assisting the Clinical Trial Managers of the group in the successful delivery of research projects. Project Administrator to join the Kadoorie Centre and contribute to the work of the Oxford Trauma and Emergency Care group. You will have demonstrable knowledge

The Clinical Trial Manager is a highly autonomous and experienced clinical operations professional responsible for all aspects of Clinical Trial Management for global studies. Oversee the creation and execution of clinical trial activities in accordance with Good Clinical Practices. Ensure complianc

To assist in the collection of data as requested by the Senior Clinical Trial Technician or Clinical Trial Pharmacists. I am very keen to hear from you if you have previously worked in a pharmacy environment and/or have some exposure to clinical trials as we have some great opportunities for you to

Demonstrates core understanding of medical terminology and clinical trial activities as it relates to the execution of a clinical development plan. Significant clinical trial management experience in the area of oncology. You love having responsibility and a say in how clinical trials are run.

Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

Plan logistics and resource usage for clinical trials, including the allocation of staff, equipment, and materials, to ensure that trials are conducted smoothly and without delays. Proven track record of managing clinical trials and delivering successful outcomes. Minimum of 5 years of experience in

Clinical Research Experience required, including at least 1 year of experience in Clinical Trial Management. Collaborates with cross functional internal and external stakeholders to ensure timely execution, budget execution of clinical trial deliverables within the country. Primary point of contact

Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Leads the development of the clinical trial strategy and delivers the clinical ope

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career

How many years of oncological therapeutic experience do you have as a Clinical Research Associate ,Clinical Lead and/or Clinical Trial Manager? Please list the oncological trials you had been working on, including the indication and phase of the trial. Demonstrates core understanding of medical term

Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials. Work with the clinical trial management staff to support

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

The role of the Senior Clinical Trial Administrator (Sr CTA) is to perform daily administrative activities and support the Project Manager(s), Project Director(s) and cross-functional study team(s) through expert knowledge and effective use of the systems, tools and processes available with a focus

Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will work with Project Coordinators and Clinical Trial Managers in the performance of clinical trial management activities. Candidates should expect to have an intensive training period and show the desire a

As a Senior Clinical Trial Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Contribute to quality Site Selection through participation in site feasibility ensuring consistent conduct of pre-trial assessment vis

Working as a Senior Clinical Vendor Manager at Parexel FSP offers tremendous long-term job security and prospects. We undertake vital clinical studies for sponsors including the leading global biotechs and Pharma top 50. In this role, you will be independently accountable for all vendor related oper

Responsibilities include coordination and conducting patient tests and visits as per the clinical trial protocol, taking informed consent, collection and preparation of biological samples, collection and entry of trial data in compliance with ICH GCP. You will develop specialist skills and knowledge

Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

The post holder will be responsible for designing, implementing, and maintaining database systems and resources for the recording of clinical trials data, ensuring that they are compliant with appropriate regulatory requirements. About you: You will have significant data management experience, withi

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. Ideally, 7 years work experience in life sciences or medically related field, including 4 years o

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. Clinical Trial Managers candidates who are ready to take a leading role in a new team of Clinical

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. Support training and supervision of junior staff, and deliver clinical trial training across teams. If you're passionate abou

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our. Communicate and collaborate on global study activities; working clo

A degree in a relevant biomedical subject and relevant work experience in clinical trial management or as a clinical research nurse. Trial Administrators are responsible for the administration and collection of clinical research data for one or more cancer trial protocols. Ensure smooth day-to-day r

Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in London. Minimum of 5 years of Clinical Trial Management experience, CRO experience preferred;. Project Manager/Clinical Tria

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

As a Clinical Trial Manager, you will join the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. BA/BS degree with at least 3 years of clinical trial experience, or an advanced degree with at least 2 years. Develop core trial documents, trial

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Represents Global Clinical Operations (GCO) within the Global Trial Team and serve

As a Clinical Trial Vendor Manager you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Working fully embedded within a growing, top 5 Pharmaceutical company, you will be independently managing all vendor related aspects o

The Opportunity:As the Clinical Trial Lead, you will be accountable for the planning, set-up and execution of assigned drug trials, which may include: pre/post-proof of concept (POC) interventional drug trials, Clinical Pharmacology normal healthy volunteer clinical trials, pre-approval access and p

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Our global Clinical Operations colleagues within our PPD clini

VP Global Clinical Trial Management. Reporting to the Senior Vice President Clinical Operations, you will be a key member of the executive leadership team, leading the Clinical Operations and Project Management functions operationally and strategically. VP Global Clinical Trial Management.

Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial. Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role. We are Worldwide Clinic

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. We are growing our Team and hiring a UK-homebased Clinical Trial Manager to work as a Clinical Ri

You will be central to the delivery of clinical trials, ensuring compliance with Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Home Office regulations. Support training and supervision of junior staff, and deliver clinical trial training across teams. If you're passionate abou

In response to emerging industry needs, we expanded our services to include Scout Clinical, one of the top providers of clinical trial patient travel and reimbursements, and Scout Academy, our secure, online, on-demand learning management system that ensures global compliance. The Scout Clinical Tri

As a Clinical Trial Manager you will take overall responsibility for the day-to-day management of multi-centre randomised clinical trials. Previous experience of working in a UKCRC registered clinical trials unit and previous involvement in development of clinical reporting forms are desirable. Exte

Provide day-to-day oversight of Clinical Research Associate (CRA) tasks on assigned projects; provide oversight of the CRA’s management of sites and monitoring of the clinical trial data; review and approve site trip reports and escalate site issues as needed to trial assigned Director, CTI execut

The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. Candidates should expect to have an

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) are vital in ensuring our clinical research programs are executed with quality and excellence, providing the care and passion patients deserve. At least 2 years’ experience as a Clinical Trial Manager, Clinical Operations Leade

The Clinical Risk Manager role demands a solid clinical trial management experience within an industry setting as you will need to demonstrate a proactive approach to managing risk in clinical research. Ideally, 7 years work experience in life sciences or medically related field, including 4 years o

Sales Executive – Pharmacovigilance/Clinical Trial IT Solutions (Life Sciences). Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharmacovigilance and Clinical Trials solutions to clients in the life sciences and healthcare sectors located in Europe, and

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Represents Global Clinical Operations (GCO) within the Global Trial Team and serve

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Our global Clinical Operations colleagues within our PPD clini

The role of the Senior Clinical Trial Administrator (Sr CTA) is to perform daily administrative activities and support the Project Manager(s), Project Director(s) and cross-functional study team(s) through expert knowledge and effective use of the systems, tools and processes available with a focus