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Ensure strict compliance with study protocols, ICH-GCP, UK Clinical Trial Regulations, MHRA guidance, and local SOPs. Solid understanding of ICH-GCP, UK Clinical Trial Regulations, and MHRA requirements.

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 Project Manager wi

Carry out all activities according to Tech Observer SOPs working within the framework of the Quality Management System and to Good Clinical Practice (GCP). Maintain awareness of new developments in programming techniques and IT which may be applied to the management and reporting of clinical trial d

Our client is an ambitious biotech developing novel therapies for serious ophthalmic diseases.Their program is entering its first-in-human clinical trial targeting wet age-related macular degeneration (wet AMD).We are seeking a seasoned freelance Medical Monitor with deep ophthalmology expertise, id

Associate Director, AI Data Scientist.AI/ML/GenAI solutions that will transform clinical trial execution and digital healthcare.This is a highly visible, strategic role with the opportunity to impact patient recruitment, real-world data generation, and next-generation digital tools across global R&D

Clinical Negligence Solicitor / Lawyer - Remote The Role This is a superb opportunity to join an award-winning Top 100 law firm that offers specialist quality legal advice to both businesses and individuals nationwide. Due to the development and expansion of the firm’s Clinical Negligence department, it is now seeking to appoint a Solicitor/Legal Executive to take on some excellent cases and work on them from inception to trial. The ideal candidate will have experience handling a caseload of Clinical Negligence claims, investigating and litigating multi-track cases. You must ensure cases are progressed in a timely, efficient and proactive manner and meet all KPI targets set by the firm. This firm currently has a team of experts and are keen to speak to likeminded people, who are passionate about Clinical Negligence and client care. The Candidate • Clinical Negligence Solicitor / Legal Executive handling own caseload (2+ years experience), • Experience of drafting legal documentation, • Prioritise and manage a varied caseload, • Ability to work well as part of a team and on your own initiative, • Excellent organisation and time-management skills, • Excellent client care skills, • Professional and effective communication with team members and contacts The Benefits & How to Apply • Salary, dependent upon experience/PQE - plus an annual bonus, • 35 days annual including bank holidays and Christmas Closure, • Hybrid and flexible working, • Ongoing training and development opportunities, • Social events and charity fundraising days, • Enhanced maternity/paternity pay Apply in the strictest of confidence online and or via telephone – there is no need for a CV for an initial conversation. Contact Roya Ratcliffe Retained Consultant – INDRR Direct Dial: 0161 826 3140 Mobile: 07376 640524

Top-5 Pharma Hybrid CLINICAL RESEARCH ASSOCIATE - Accelerate Innovation & Shape the Future of Medicine. Proven CRA Expertise: Minimum of 2-4 years of experience as a Clinical Research Associate, demonstrating a strong understanding of clinical trial processes and a track record of successful site mo

Hobson Prior is seeking a Japanese-speaking freelance clinician to support clinical trial activities in Alzheimer's Disease. Proficiency in both written and spoken Japanese (language verification may be required).

Demonstrable experience leading clinical aspects of your studies across multiple countries in a CRO / Pharma or Biotech company (in a dedicated 'clinical lead' role). Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Demonstrates core understanding

Clinical Trial Liaison – Oncology (Europe, Field-Based).An innovative global biotech company is seeking a Clinical Trial Liaison to drive site and patient engagement for oncology trials across Europe, with a focus on breast cancer and other high-priority indications.Build relationships with KOLs,

Senior Clinical Genetics Lead, manchester. 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,.

Ensure that data is available and up to date for any meetings related to a clinical trial in collaboration with the Senior Clinical Trials Coordinators. Assist with general preparation for audit and inspections within assigned teams, under the direct supervision of the Senior Clinical Trials Coordin

A Scientific Officer (Quality Assurance) is required for our higher education client to join their quality assurance team within their research centre to contribute to their compliance by assuring that their clinical trial activities comply. A Scientific Officer (Quality Assurance) is required for o

This position is suitable for an enthusiastic and research-motivated applicant with a Medical degree and experience in head and neck/salivary cancer who can demonstrate commitment to a career in Medical/Clinical Oncology and have an interest in gaining further research and clinical trial experience

We are seeking an enthusiastic, motivated and experienced individual who will be responsible for assisting a team of Clinical Trials Coordinators, Research Nurses, and Investigators with various aspects of clinical trial administration/ coordination. Provide administrative support to the Clinical Re

The Clinical Scientist supports the design, execution, and analysis of clinical trials that are part of AIRNA’s RNA editing platform. Working closely with Clinical Development, Clinical Operations, and external clinical trial site staff, the clinical scientist will ensure scientific integrity and

We run one of the largest early clinical trial units in Europe with over 300 trials every year. Provides appraisal/performance review of all administrative staff resulting in clearly understood objectives and personal development plans that reflects both the needs of the Trust and the longer-term go

This position is suitable for an enthusiastic and research-motivated applicant with a Medical degree and experience in head and neck/salivary cancer who can demonstrate commitment to a career in Medical/Clinical Oncology and have an interest in gaining further research and clinical trial experience

The post is designed to provide specific education and training in Interventional imaging, particularly Interventional Radiology, with access to online modules, cases, and protected reporting sessions. The institute is an international leader in research, with a large early clinical trial unit condu

Support contract negotiation processes with trial sponsors under direction from the Clinical Research Nurse Team Leader/ Research Manager, ensuring appropriate financial agreements are in place for each project for both commercial and Trust-sponsored (i. However, the Research Divisions managerial te

Experience in the clinical/healthcare industry, preferably clinical research. Strong understanding of the clinical trial process and clinical trial protocols. In response to emerging industry needs, we expanded our services to include Scout Clinical, one of the top providers of clinical trial patien

The successful candidate will be a team player with strong clinical presence, excellent communication skills, and the ability to work autonomously. We are also an international leader in research, with a highly active clinical trial unit and a strong reputation for cancer research in the UK.

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.