As the hub of central intelligence for studies, you will lead CRAs and oversee all clinical aspects of your study across multiple countries, ensuring timeline adherence and scope, whilst ensuring quality delivery; addressing the challenges facing the research and development of novel compounds in Oncology and dedicated to positively impacting the health and lives of patients around the world.
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As a Clinical Trial Manager you will be joining the worldβs largest & most comprehensive clinical research organisation, powered by healthcare intelligence. You will assume responsibility for an individual project, or many projects and communicate in an optimal way, making sure that specific client objectives are met. Responsible for the set-up and maintenance of the project(s).
Consultant needed to design a detailed implementation plan for the roll-out of the MFT strategy in Rwanda, aligning with national malaria strategic plan, Jhpiego-supported interventions, and international best practices. Over a period of 10 working days, the consultant will conduct reviews, consult with stakeholders, assess ACT deployment, and draft a costed implementation plan.
As a GPhC-registered Pharmacy Technician, youβll play a vital role in delivering safe, high-quality care through remote clinical services for Numanβs patients. Youβll work alongside pharmacists and clinicians to review treatments, maintain accurate clinical records, and provide clear, empathetic guidance to patients about their medications. As part of a multidisciplinary team, youβll also help manage digital workflows, support safe prescribing practices, and use innovative tools to ensure care is efficient, accessible, and patient-centred.
The clinical pharmacist telepharmacy provides timely, accurate, and complete pharmaceutical care by performing pharmacist functions using standard techniques to process medication orders. This individual provides drug information, keeps pertinent records, oversees medication preparation, and monitors for adverse reactions, allergies and appropriate medication use. They also use clinical skills to monitor medication selection and communicate with site staff for clarifications.
This role inputs computer data entry of medications and medical records into clientβs Electronic Medical Records (EMR) System. Responsibilities include entering medication orders and medical records accurately and timely, processing orders at a minimum productivity standard, and contacting clients for order verification. The technician will also prioritize order entry, perform reconciliation of EMR orders, and report discrepancies to the supervisor.
Oversee medical safety activities and processes for assigned products, ensuring continuous assessment of safety profiles and benefit-risk of investigational and marketed compounds. You will provide strategic, patient-focused leadership for medical safety, support asset strategies, and strengthen medical and scientific innovation. Timely escalation of safety issues to the Takeda Safety Board Chair is required.
The Drug Safety Physician will be responsible for the pharmacovigilance function, including medical review and oversight of processing for all types of safety events. The individual will provide clinical support of drug safety data management and interpretation and risk management activities for the company. This includes oversight of clinical trial Serious Adverse Event (SAE) processing and safety data analysis to support signal detection and risk/benefit profile evaluation.
This is an exciting opportunity for a freelancer / consultant to join our team as Local Safety Officer in France. By working with us, you will have the opportunity to work in an international team and strengthen your expertise within the broad and diverse PV and Regulatory Affairs area.
At Illumina, you will lead global access strategies for our portfolio of diagnostic solutions pediatric and adult genetic disease as well as a portfolio of reproductive health solutions. Your work will help ensure that individuals and families around the world can benefit from early, accurate, and equitable access to life-changing genomic insights. This is a high-impact, strategic leadership role that requires deep expertise in diagnostic testing for rare and inherited conditions, and reproductive health.