Job Overview Direct, oversee and manage complex labeling and regulatory projects, ensuring quality deliverables on time and within budget. Ensure that all project work is completed in accordance with standard operating procedures, policies and practices. Essential Functions
Job Description Are You Ready to Make an Impact at RSSL? Join Our Mission to Transform Lives Through Science, Innovation and Collaboration At Reading Scientific Services Ltd (RSSL), we lead the way in scientific analysis, research,
Overview Our Employment team in Reading are looking to recruit a 5-8 year PQE Associate to join the team. The successful candidate will be based in and support the partners in Reading and across all offices when
Sr. Site Contracts Associate IQVIA Biotech UK - Homebased IQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. agile structure, collaborative culture, and deep therapeutic expertise
IQVIAs Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK Apply
Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions. Influence and
CRAII - Oncology UK ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. Why IQVIA? Career development opportunities to grow as we grow AI‑powered career
Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. With access to world-class training and professional development, we’ll give you the tools you need to
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA UK’s cFSP (sponsor-dedicated) team is growing and seeking experienced Clinical Research Associates. Why IQVIA? Career development opportunities to grow as we grow Flexible working
Join Us on Our Mission to Drive Healthcare Forward IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK. Why IQVIA? IQVIA is recognized as #1 in its category on the 2025 Fortune® World’s Most
Senior CRA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at
At a Glance Legrand has an exciting opportunity for an EHS Specialist to join the Starline Team in Reading, UK. The EHS Specialist will be responsible for facilitating compliance and delivery of the company occupational policies
Role: Regulatory Associate – CTA Contract: 12-month rolling Office- Maidenhead (hybrid) – 3 days on site SRG are partnered with a global biopharmaceutical company with focus and capabilities to address some of the world’s greatest health challenges. Our
About Freyr Freyr is a global Regulatory Solutions and Services organization supporting Life Sciences companies across Regulatory Affairs, Clinical, Safety, and Compliance. We partner with leading pharmaceutical, biotechnology, and medical device companies, delivering end-to-end regulatory operations support and regulatory strategy
Reading, Berkshire, United Kingdom Full time R To lead Local Study Teams (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international
Reading, Berkshire, United Kingdom Full time R The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning,executing, and reporting, (from first site initiation visit to and including study site close-out), of assigned studies in
Basic information Location Birmingham, Bristol, Cambridge, Leeds, London, Manchester, Reading Business Line Tax & Legal Job Type Permanent / FTC Date published 10-Jul-2026 Req # 22669 Job description Connect to your IndustryOur national Reward business represents
Job DescriptionIQVIA Biotech has an exciting position within its EU Biostats team. As the Biotech and Emerging Biopharma arm of IQVIA, we continue to grow and win new business. Historically IQVIA Biotech focused on Oncology, Dermatology
Employement Associate - Highly Respected International Firm A highly regarded, Legal 500 and Chambers recognised law firm , with an established reputation across the UK legal market, is looking to appoint a 5+ PQE Employment Associate to join