7 jobs found in Thornton Heath

Our client, a global pharmaceutical company, is currently looking for a Clinical Trials Supply Chain Manager to join their team in Uxbridge on a full time, 6-month temporary basis (35 hours per week). This role is expected to be worked on a hybrid basis but remote applications will also be considered. You will be responsible for managing the supplies for the clinical trials and/or drug development whilst ensuring that this is done in a cost-effective and timely manner. Key Responsibilities Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and cost-efficient manner Developing and managing forecasting and clinical protocols along with demand and planning of clinical supplies Create clinical development timelines and proactively identify strategies and solutions for any issues that may arise Support the creation of medical protocols drafts and in the developing of package and label outlines Act as the clinical supplies point...

Talentmark is recruiting for a Country Study Start Up Lead to join a company in the Pharmaceutical industry, at their site based in Welwyn Garden City, on a contract basis for 6 months. Salary: Daily: £339 - £376.97 PAYE or £450 - £500 per day Umbrella. Country Study Lead Role: Drive and facilitate efficient study start-up processes to contribute to the delivery of clinical trials to patients. Leading the country strategy for study start-up, driving efficiency, innovation, and collaboration with external stakeholders. Overseeing start-up operations and ensuring timely and efficient site activation and regulatory compliance. Engaging with government and institutional bodies to align on clinical trial policies and practices (e.g., with Ethics Boards, Health Authorities).Your Background: Degree (MD, PhD, MA/MS, BA/BS) in life sciences or equivalent. Postgraduate degree or master’s degree highly desirable Demonstrated experience in clinical trial start-up, regulatory...

Study Start-Up Lead (SSUL) - External Job Description (6 month contract) Purpose & Role Overview The Study Start-Up Lead (SSUL) plays a central role in driving efficient and high‑quality study start-up activities to support the delivery of clinical trials. This position leads and coordinates the processes that enable timely trial initiation, supporting innovative trial delivery across multiple therapeutic areas. You will work closely with local and global teams, clinical sites, external partners, and vendors to ensure a seamless start-up experience for investigators, site staff, and study participants. Key Responsibilities Study Start-Up Strategy & Execution Lead the development and execution of country-level study start-up strategies. Drive efficiency, innovation, and proactive risk mitigation throughout the start-up process. Collaborate with internal stakeholders, global study teams, and CRO partners to ensure alignment with overall study plans and timelines. Ensure...

Talentmark are recruiting for a Senior Patient-Centered Outcomes Research Scientist to join a company in the pharmaceutical industry on a contract basis for 9 months. Salary: £75 – £90 per hour (Outside IR35) Senior Patient-Centered Outcomes Research Scientist Role: Develop and implement patient-centred, fit-for-purpose measurement strategies across the drug development lifecycle Collaborate with global study teams, lifecycle teams, and cross-functional stakeholders to integrate patient-focused outcomes into clinical development Support study start-up, monitoring, and close-out activities related to clinical outcome assessments (COAs) Lead or contribute to the implementation of electronic COAs (eCOA), including user acceptance testing, linguistic validation, and file specification reviews Assess and drive the development or deployment of new measurement tools to capture patient experience effectively Provide subject matter expertise in areas such as digital measurement...

Role Name: Laboratory Technician Site location: Stevenage, UK Hourly Rate: £16 per hour via PAYE Duration of contract: 6 months initially, possibility for extension. Weekly hours: 37.5 hours LABORATORY TECHNICIAN (CHEMISTRY R&D) STEVENAGE Help us improve access to life-changing therapies that can transform human health A global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020. Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups, and sauces - they need to work better, faster, and safer, leading to better patient outcomes. We are looking for an organized, self-motivated, enthusiastic, and...

Are you a motivated Clinical Pharmacist looking for a role where you can make a genuine impact on patient care? We’re supporting a leading, well-established healthcare organisation in the search for an exceptional pharmacist to join their clinical pharmacy team. This is a fantastic opportunity to work within a modern, high-performing hospital environment known for delivering outstanding patient outcomes. The Role As a key member of the multidisciplinary team, you will: * Conduct detailed medication reviews for inpatients and outpatients, ensuring safe, effective, and evidence-based use of medicines. * Provide personalised advice to patients on treatment plans, side effects, and adherence. * Review and authorise prescriptions in line with clinical guidelines and regulatory standards. * Promote safe, cost-effective prescribing by supporting compliance with local and national medicines policies. * Contribute to antimicrobial stewardship initiatives and monitor high-risk...

We are seeking a Process Technician to support production operations within a pharmaceutical GMP-regulated environment. This role involves operating and monitoring manufacturing equipment, maintaining batch documentation, and ensuring compliance with pharmaceutical quality, safety, and hygiene standards. Key Responsibilities * Operate and monitor production equipment in line with SOPs and GMP requirements. * Carry out raw material charging, equipment setup, cleaning, and basic maintenance. * Maintain accurate batch documentation and production records. * Identify and report process deviations and support resolution activities. * Support continuous improvement and updates to procedures where required. * shift work will be required Requirements * Experience in pharmaceutical, GMP, or manufacturing environments preferred. * Strong attention to detail and ability to follow procedures. * Good communication and teamwork skills