Clinical Research Coordinator jobs in Reading

Job Description CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The Director Clinical...

Are you an experienced GP with a passion for clinical education, digital innovation and improving the appraisal experience for healthcare professionals? Do you want to shape the future of clinical learning and make a real impact on the careers of tens of thousands of clinicians across the UK? If so, this could be the perfect opportunity for you. We’re looking for a dynamic Clinical Education...

Job Description Company Description Synthesis Clinic is a specialist-led practice blending contemporary precision medicine with evidence-based nutrition, lifestyle support, psycho-emotional wellbeing, and complementary therapies. Founded by Dr. Nina Fuller-Shavel, the clinic has an award-winning approach to women’s health and integrative cancer care, emphasizing empowerment, expertise, and...

THE POSITION External Research & Named Patient Co-ordinator 12 months contract We have an exciting contract opportunity for an External Research & Named Patient Co-ordinator to support the oversight and operational delivery of External Research activities (Investigator Initiated Studies (IIS) and External Collaborative Research (ECR)) alongside the coordination of the supply of Boehringer...

A leading global clinical research provider is seeking a Medical Strategy Lead specializing in Cardiovascular studies. The role requires a Board-Certified cardiologist with over 2 years of clinical research experience. Responsibilities include creating innovative strategies for clinical trials and providing scientific expertise across divisions. The ideal candidate has strong clinical,...

You will be responsible for managing clinics on the BEST4 mobile unit and will be trained to administer the Capsule Sponge test.

You will work alongside established clinical teams, researchers, research nurses, research practitioners and administrators to facilitate recruitment, sample collection, data entry and providing clinical support as required.

You will need the following: - Right to work in the UK - Up to 2 years pharmaceutical industry experience or other relevant experience (NHS or Academic) - Good knowledge of drug development process specifically clinical trial/research - Knowledge of international standards (GCP/ICH, FDA, EMEA)

You will coordinate bid activity from the opportunity stage through to submission, taking ownership of smaller bids and defined elements of larger, more complex tenders.

Sales Development Representive - Part-time, Contract or Full-time. Remote or HybridAt FISCAL Technologies, we're not just selling software – we're partnering with finance leaders to protect over £350 billion global spend every year through innovative AI-driven solutions that deliver ROI within three months.We need passionate relationship builders who can open doors, book meetings and help develop...

At STADA we pursue our purpose “Caring for people‘s health as a trusted partner” worldwide. Originally founded by pharmacists, we are a leading manufacturer of high-quality pharmaceuticals. More than 12,300 employees around the globe live our values Integrity, Entrepreneurship, Agility and One STADA to achieve ambitious goals and shape the successful future of STADA. Britannia Pharmaceuticals,...

You will be supported by the Principal Psychologist to manage a clinical caseload and contribute to service delivery.

You will offer (neuro)psychological assessment and intervention to adults with stroke. This will include undertaking: - cognitive and mood screening, more detailed neuropsychometric testing,

You will be involved in drafting documents, conducting research, and liaising with clients and medical professionals. This role offers hybrid working, comprehensive benefits, and significant career growth opportunities in a supportive culture that values development and teamwork.

Paralegal (Clinical Negligence – Reading) Location: Reading / Hybrid Turn Your Legal Skills Into Life‐changing Results. Join Fletchers Group, where a supportive culture meets meaningful work. We're seeking a Clinical Negligence Paralegal to manage a supervised caseload, assist senior solicitors, and work on complex, often life‐changing cases. You'll draft documents, conduct research, liaise with...

Select how often (in days) to receive an alert: Create Alert Field Clinical Specialist, CRM (West London & South Central England) Work mode: Field Based Territory: United Kingdom Additional Locations: United Kingdom-Reading; United Kingdom-Basingstoke; United Kingdom-Camberley; United Kingdom-Guildford; United Kingdom-Slough; United Kingdom-Woking Diversity - Innovation - Caring - Global...

Job Description CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, were building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. The role Were looking...

Join IQVIA on Our Mission to Drive Healthcare Forward! IQVIA's Real World Evidence team are seeking a Clinical Research Associate (CRA I OR CRA II) to support Phase 3b and Phase 4 studies across a diverse range of therapeutic areas. The position is UK based and offers remote working with travel to sites across the UK and Ireland. Why IQVIA? IQVIA is recognized as #1 in its category on the 2025...

You will be an enthusiastic, suitably skilled and experienced health care professional to undertake the role of Clinical Lead Occupational Therapist for the Learning Disabilities Service.

You should be self-motivated with excellent organisational skills and the ability to prioritize your workload.

Join Us on Our Mission to Drive Healthcare Forward As a Clinical Research Associate at IQVIA, you’ll play a vital role in advancing clinical research and improving patient outcomes. We’re expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to...

Job Overview Support quality issues management, Customer Audit/ Regulatory Inspections report response management , Corrective and Preventative Action (CAPA) and Effectiveness Check (EC) plan review, approval and closure. Provide consultation in interpretation of regulations, guidelines, policies, and procedures. Support management in promotion and assessment of compliance to regulations,...

The Sr. CDM will lead and contribute to data management activities in support of Client's studies across all stages of clinical drug development. Summary of Key Responsibilities Contribute to data management activities as a lead study data manager in support of Client's clinical studiesLead database build activities including leading cross-functional review of eCRF content, review of edit check...