Future Tech Jobs
Future Tech Jobs
The Role:Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases.As an employee, you'll be part of a continually growing organization...
The Commercial Associate Director will lead contract negotiations, manage strategic client relationships, and drive proposal and bid management for Nuclera's lab services. Key responsibilities include pricing discussions, managing key accounts, and developing commercial strategies to support market expansion and revenue growth.
This role involves leading an analytical team in early chemical development, ensuring the delivery of high-quality analytical work to support GMP manufacturing and stability. The position requires extensive experience in analytical science, a passion for team development, and the ability to drive organizational effectiveness and innovation.
This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position shapes operational strategy, drives innovation in trial design, and ensures delivery across a diverse asset portfolio. It involves leading vendor partnerships, managing regulatory and quality compliance, and developing clinical teams within a patient-ambitious, data-driven environment.
Your work will change lives. Including your own.The Impact You’ll Make:Recursion is currently seeking a seasoned leader to join our team as Vice President, Real World Experience. This role will lead RWE generation across the Recursion portfolio. The role will...
The Validation/Quality Assurance Specialist will plan and execute validation activities, author and maintain validation protocols, and collaborate with cross-functional teams to ensure compliance with GMP standards. The role involves maintaining validated status, supporting regulatory inspections, and contributing to the Site Validation Master Plan.
This role leads clinical operations for complex, multi-indication assets in hepatology, renal, and cardiovascular disease, with strategic oversight of global Phase III trials, rare disease programmes, and co-development partnerships. The position involves shaping operational strategy, managing high-level vendor relationships, and driving innovation in trial design including decentralised and hybrid models. It requires leadership in risk management, data-driven decision-making, and team development within a global regulatory and compliance framework.
This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives end-to-end operational strategy, including country and site selection, patient recruitment, risk management, and vendor oversight, while ensuring alignment with clinical development and evidence generation plans. It also involves direct leadership of clinical teams, fostering innovation in trial design, and maintaining inspection readiness across the portfolio.
This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position involves shaping operational strategy, managing CRO partnerships, and driving innovation in trial design while ensuring quality and compliance. Leadership includes direct management of clinical teams and strategic input into asset development across the R&D pipeline.
This role leads clinical operations for complex, high-impact assets in hepatology, renal, and cardiovascular disease, with responsibility for global Phase III trials, rare disease programmes, and co-development partnerships. The position involves setting operational strategy, managing CROs and vendors, driving data-led decision-making, and ensuring trial delivery to time, cost, and quality. It also includes direct leadership of clinical operations teams and integration of innovative trial methodologies.
This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives operational strategy, risk management, and innovation in trial design, while managing senior vendor relationships and developing clinical teams. It emphasizes data-led decision-making, enterprise-wide impact, and compliance across a global development portfolio.
This role involves ensuring compliance with Good Distribution Practise (GDP), ISO 9001, and ISO 13485 standards through quality assurance activities such as managing deviations, change controls, audits, and supplier verifications. The Quality Officer will support the Quality Management System, conduct investigations, review documentation, and prepare for regulatory inspections. They will work closely with internal teams and external stakeholders to maintain product quality and process safety in a regulated environment.
The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also supports site selection, protocol training, and continuous improvement initiatives to enhance clinical trial execution.
As Clinical Data Analytics Lead, you will transform complex clinical trial data into actionable insights, enhancing decision-making and data quality. You will collaborate with cross-functional teams to drive risk-based approaches, improve study oversight, and support patient outcomes using advanced analytics and visualization tools.
The Global Development Lead will drive clinical research for cardiometabolic diseases, creating and executing early clinical development strategies. They will work closely with cross-functional teams to translate pre-clinical observations into clinical experiments, ensuring medical and scientific excellence, and managing the delivery of clinical trial data and regulatory documents.
