The Feasibility Manager will deliver evidence-based feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements, producing country, site, patient-pool, and recruitment recommendations. The role requires interpreting clinical and epidemiological data, conducting site and landscape analyses, presenting findings to stakeholders and clients, and collaborating across functions to support global clinical-trial feasibility.

Precision for Medicine is hiring a Feasibility Manager (or Senior Feasibility Associate depending on experience) to deliver country, site, patient-pool, and recruitment recommendations for pre-award, post-award, rescue, and standalone feasibility engagements. The role requires interpreting clinical and epidemiological data, performing site and landscape analyses, presenting findings to stakeholders and clients, and contributing to feasibility methods and tools. Requires a bachelor's in life sciences (or related), professional English, and a minimum of two years' relevant experience.

Precision for Medicine seeks a Feasibility Manager (or Senior Feasibility Associate depending on experience) to deliver country-, site-, and patient-pool feasibility analyses for pre-award, post-award, rescue, and standalone engagements. The role requires clinical/scientific interpretation, operational intelligence, data synthesis, and collaboration with Business Development, Clinical Operations, Medical teams, and external partners. Minimum two years' relevant experience and professional proficiency in English required.

Join the Elasticsearch Search team to lead the design and implementation of vector search capabilities, improve relevance and performance, and contribute to Lucene improvements. The role requires expert-level Java, professional experience with vector similarity/vector databases (HNSW, IVF or similar), algorithm and data-structure work, and experience collaborating in distributed/open-source teams.

Manager responsible for leading and mentoring a global team that handles end-to-end site payment management, ensuring timely fund setup and invoice payments, implementing process improvements, and producing regular reporting. Requires minimum 7 years' professional experience (CRO, finance/accounting or comparable) and at least 1 year of management experience; advanced English proficiency expected.

The Senior Operations Specialist will lead process improvement and change management initiatives to improve delivery of studies for Sponsors. Responsibilities include business-process evaluation, root-cause analysis, designing and implementing process changes, stakeholder communication, training support, documenting processes, and establishing performance metrics. Requires 5+ years relevant experience and strong English communication; experience in CRO/pharmaceutical/biotech drug development and knowledge of ICH-GCP are specified.

The Project Support Specialist will provide cross-functional support to project teams for clinical studies, including maintaining project timelines (MS Project), CTMS activities, organizing meetings and minutes, managing training records and user access, establishing SharePoint sites, preparing study binders and trackers, and assisting with safety report distribution and study communications. Requires a 4-year degree or equivalent, minimum 2 years relevant experience, and professional-level English (C1).

Precision for Medicine is hiring a Clinical Project Manager / Senior Clinical Project Manager to manage end-to-end (ph I-IV) Oncology trials in a CRO setting. Responsibilities include full-service project oversight, client liaison, proposal/costing activities, managing budgets and timelines, coordinating functional areas (data management, safety, clinical, medical monitoring, biostatistics), and preparing study documentation. Role requires at least 4 years' full-service project management experience in clinical trials and working knowledge of GCP/ICH.

Parexel seeks an experienced Clinical Project Leader or Senior Project Leader to manage global biotech clinical trials across select EMEA countries (remote). Role requires strong CRO clinical trial project management (Phase I–III), Oncology expertise (required), familiarity with ICH/GCP, financial and client relationship management, and leadership of cross-functional teams.