Postdoctoral Research Associate jobs in Reading

Full time. fixed term until (31/10/26) Closing Date: 23:59 on 5th December 2025 Interview Date: 15 December 2025 By reference to the applicable SOC code for this role, sponsorship may be possible under the Skilled Worker Route. Applicants wishing to consider the SWR must ensure that they are able to meet the points requirement before applying. There is further information about this on the UK...

- Job Title: Lead Clinical Research Associate - Location: Remote in UK - Salary: £56,000 - £63,000 (DOE) - Additional Benefits: Car allowance (or company car) and bonus - Sign-on Bonus: Potential sign-on bonus for qualified candidates - Company: Global CRO RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing...

You will receive a comprehensive induction, training, and awareness sessions to support your effectiveness in the role - A commitment to provide the time (circa 20 days per annum) and energy required is essential.

You will work with telecommunications data including time series, network telemetry, and sensor data to address complex operational challenges in wireless technology.

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)

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...

MissionSupport clients from corporations, consulting firms, and investment funds in addressing critical decision-making challenges by quickly identifying and connecting them with the most relevant industry experts and ensuring the successful execution of one-on-one online consultations. Remove barriers to knowledge and enable decisions based on first-hand insights.ResponsibilitiesUnderstand...

You will work within the standards provided in the OFG Speech and Language Therapy Ways of Working.

You will be given responsibility for holding a Speech and Language therapy caseload, with the full support of your designated clinical supervisor and site lead, also contributing to staff training and consultation as required This post would suit a resilient, creative and enthusiastic individual.

You will kick off your career at VISASQ/COLEMAN with a comprehensive 12-week training program, designed to prepare you to independently work as an Associate as a member of our Client Management team. The start date for this role is still to be determined. Key Responsibilities Post-Training Academy Completion:

You will relish being part of dynamic team within a progressive and well-respected firm. Good communication skills and an enthusiasm for working within a team environment. Like us, to be serious about sustainability.

Pharmacovigilance Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a...

You will be trusted to run matters independently, think commercially, and deliver work to a high standard with minimal supervision. Commercial contracts experience is an advantage, but strong corporate capability is essential. The work is varied, often complex, and frequently cross-border.

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...

Pharmacovigilance Associate (Office based) ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team....

Permanent, full-time or part-time The closing date for applications is 23.59 on 8th December 2025 Due to the complexity of the Skilled Worker Visa route and eligibility criteria, applicants requiring sponsorship are recommended to check their eligibility on the Home Office website. We cannot provide advice to candidates at the application stage and will only discuss visa routes with candidates...

- Job Title: Senior CRA / Senior CRA II - Location: Remote in UK - Salary: £53,000 - £59,000 (DOE) - Additional Benefits: Car allowance (or company car) and bonus - Sign-on Bonus: Potential sign-on bonus for qualified candidates - Company: Global CRO RBW Consulting is thrilled to present an exciting opportunity on behalf of one of our esteemed clients. As one of the few rapidly growing Contract...

Senior Project Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Project Associate to join our diverse and dynamic team. As a Senior Project...

Job Title: Senior CRA / Senior CRA II Location: Remote in UK Additional Benefits: Car allowance (or company car) and bonus Sign-on Bonus: Potential sign-on bonus for qualified candidates As one of the few rapidly growing Contract Research Organizations (CROs) for UK studies, our client is expanding their site management team with multiple hires this year. They are involved in a diverse range of...

You will become part of a vibrant and distinguished community of scholars, including Mark Casson, Davide Castellani, Rajneesh Narula and Alain Verbeke, whose work continues to shape the discipline, alongside a dynamic group of emerging academics. We welcome applications from academics who can demonstrate:

Full time, Fixed Term contract for 30 months Closing date 5 January 2026 Interviews will be held:21st January 2026 By reference to the applicable SOC code for this role, sponsorship may be possible under the Skilled Worker Route. Applicants wishing to consider the SWR must ensure that they are able to meet the points requirement before applying. There is further information about this on the...