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
Associate Account Manager Role objective: Reporting to the Associate Director, Account Management, this role supports the day to day delivery of selected projects and programs, providing high quality financial and project coordination, documentation and tracking to enable the
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
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
At a Glance Legrand has an exciting opportunity for an Applications Engineering Drafter I to join the DPC Starline UK Team. This position reports to Reading, UK. The AE Drafter II plays a key role in
POSITION SUMMARY The Contract Compliance Senior Manager EMEA will report to the Senior Director Contract Compliance EMEA. This is an important role on the EMEA Finance team, ensure compliance with contracts/agreements, training key users on the
POSITION SUMMARY This position is responsible for the execution of revenue management processes and strategies that meet the company’s mission, standards and focus on continuous improvement, supporting the RMS Senior Leadership team to drive growth and
At a Glance Legrand has an exciting opportunity for a Planner to join the Starline Team. This position reports to Reading, UK. The Planner is responsible for the day-to-day planning, scheduling to support customer orders. This
+ 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.
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.
Senior Cost Manager - Reading A well-established multidisciplinary built environment consultancy is looking to appoint an experienced Senior Cost Manager to join their Reading team. This is an excellent opportunity for a Senior Cost Manager to