Precision for Medicine seeks a Contracts Manager (APAC) to lead site contract management across APAC, including drafting, reviewing, negotiating CTAs, vendor contracts and site budgets, developing contracting strategies, and working closely with Clinical Operations and sponsors. Requires minimum 5 years' relevant experience in CRO/life sciences and fluency in English. Remote roles listed for China and Singapore.

Principal Clinical Business Analyst responsible for planning, designing, implementing and driving adoption of Business Operation Systems to support clinical study delivery. Requires ~8 years' relevant experience, expertise with clinical trial systems (CTMS, EDC, eTMF, RTMS), requirements gathering, configuration, integrations, testing/UAT, training, change management, stakeholder engagement and supporting audit/CAPA activities. Remote role based in Hungary, Poland, Romania, Serbia or Slovakia.

Lead the planning, design, development, implementation and adoption of Business Operation Systems to support clinical study delivery, including requirements gathering, configuration, testing (UAT), integrations, training and change management. Role requires experience with clinical trial systems (CTMS, EDC, eTMF, RTMS), experience in transforming business requirements into functional requirements, leadership experience, and effective English communication; Bachelor’s degree plus 8 years of relevant experience.

Principal Clinical Business Analyst responsible for planning, design, implementation and adoption of Business Operation Systems to support clinical study delivery. Role requires at least a bachelor's degree plus 8 years' relevant experience, expertise with clinical trial systems (CTMS, EDC, eTMF, RTMS), requirements gathering, configuration, integrations, UAT, training and change management. Salary estimate for Poland: 173,000 PLN - 259,400 PLN gross per annum.

Seeking a Principal Clinical Business Analyst with a minimum of 8 years' relevant experience to lead system implementation, requirements gathering, configuration, integrations, testing (including UAT), training and adoption for clinical trial systems (CTMS, EDC, eTMF, RTMS). Role is remote and based in Hungary, Poland, Romania, Serbia or Slovakia and requires effective English communication and experience in clinical operations and change management.

The Principal Clinical Business Analyst leads design, configuration, testing and adoption of clinical Business Operation Systems (e.g., CTMS, EDC, eTMF, RTMS). Responsibilities include requirements gathering, system implementation and integrations, UAT, training and change management, stakeholder engagement, audit/CAPA support, and using data/metrics to monitor adoption. Requires a bachelor's degree (or equivalent) plus 8 years of relevant experience and prior clinical operations/system experience.

Experienced Senior In-house CRA role supporting investigator sites and clinical project teams across LATAM. Responsibilities include site identification and feasibility, maintenance of investigator site files and TMF, use of CTMS/EDC/TMF systems, site liaison and monitoring (including remote activities), data review and database closure support, study supply and sample logistics, training/mentoring junior staff, and ensuring compliance with ICH-GCP, SOPs and local regulations. Remote role with travel as needed; requires minimum 4 years clinical trial experience and fluency in English.

Seeking a Marketing and Events Manager to lead planning, execution, and optimization of conferences, trade shows, webinars and field activations. Requires 5+ years of B2B event experience (pharma/life sciences preferred), proficiency with HubSpot and Salesforce, strong project and vendor management skills, and some travel to major trade shows.

The Senior Finance Analyst – Clinical Solutions Portfolio delivers portfolio-level financial analysis for Clinical Solutions departments, leading project financial oversight across the project lifecycle and performing variance analysis to identify drivers, scope creep and risks. The role partners with project finance and operational teams, develops trial operations KPIs that link operational performance to financial outcomes, and builds Excel and Power BI dashboards for governance and executive review. Requires a bachelor's degree and a minimum of 5 years' related experience, with strong Excel and Power BI skills and preference for CRO/clinical research experience.

Accountable for end-to-end delivery of assigned clinical study projects in oncology, including client liaison, vendor coordination, budget and financial oversight, project planning, risk and quality management (eTMF inspection readiness), and cross-functional collaboration. Requires experience with Microsoft Office, Microsoft Project, eTMF, EDC, CTMS, knowledge of ICH-GCP, and prior pharmaceutical/device research experience. Position may require domestic and international travel.

Responsible for preparation and submission of clinical trial dossiers (initial and amendments), interaction with Competent Authorities and Ethics Committees, maintenance of project plans/trackers, coordination with CRAs and other functions for site activation, translation coordination, TMF/document management, and support for feasibility, contract and budget negotiations. Requires a bachelor’s in life sciences or equivalent, at least 1 year relevant experience, and fluency in English.

Precision for Medicine is hiring a Clinical Research Associate I/II for Turkey (fully home-based possible). The CRA will monitor and manage clinical study progress at investigative sites, support study set-up (investigator ID, regulatory submissions, initiation visits), ensure compliance with protocol, SOPs and ICH-GCP, and identify/mitigate study risks. Minimum required: university degree in life sciences/health-related discipline or equivalent, and at least 6 months of CRA or equivalent clinical research experience; oncology monitoring experience preferred. Role involves significant travel (up to ~60% on average) and requires fluency in English and Turkish.

Precision for Medicine seeks a CRA I/II for a remote position based in France (Paris area). The role requires at least 1 year of CRA experience (CRO or industry), experience managing oncology studies, monitoring and site management responsibilities, ensuring compliance with protocol, SOPs and ICH-GCP, coordinating study start-up and regulatory activities, and availability for substantial domestic travel (up to ~50–60%). Fluency in English and the local language (French) is required.

Remote Clinical Trial Manager role in a precision medicine CRO responsible for operational delivery of clinical trial elements (site selection, start-up, enrolment, monitoring, data cleaning, close-out) across multiple countries. Requires experience leading multi-country clinical studies (oncology), working knowledge of GCP/ICH, ability to travel internationally, and effective English communication.

Manage and deliver clinical trial activities across multiple countries including site selection, start-up, enrollment management, monitoring, data cleaning and close-out. Role requires significant oncology trial management experience in a CRO/Pharma/Biotech setting, working knowledge of ICH-GCP, ability to mentor CRAs, and availability for domestic and international travel.

Precision for Medicine seeks a Clinical Trial Manager (remote) to manage and operationally deliver clinical elements of oncology trials across multiple countries (UK, Hungary, Poland, Romania, Serbia, Slovakia). Responsibilities include site selection and start-up, enrolment management, monitoring, data cleaning, close-out, leading CRAs, regulatory documentation, and cross-functional communication. Requires demonstrable multi-country clinical lead experience in a CRO/Pharma/Biotech setting, strong knowledge of ICH-GCP, and effective English communication. Availability for domestic and international travel is required.

Experienced Clinical Trial Manager role (remote) within a precision medicine CRO focused on oncology and rare diseases. Candidate will manage clinical elements across multi-country trials including site selection, start-up, enrolment management, monitoring, data cleaning and close-out; lead and mentor CRAs; ensure communication, regulatory oversight and adherence to ICH-GCP and company SOPs. Bachelor’s degree in a science or health-related field is required; significant clinical trial management experience in oncology and availability for domestic/international travel are expected. Required familiarity with CTMS, eTMF, EDC, IXRS and MS Office tools.

Precision for Medicine seeks an experienced Clinical Trial Manager to lead clinical aspects of multi-country oncology and rare-disease trials. Responsibilities include site selection, start-up, enrollment management, monitoring oversight, data cleaning, close-out, leading CRAs, and ensuring regulatory documentation and timeline adherence. Role requires demonstrable clinical trial management experience in CRO/Pharma, working knowledge of ICH-GCP, and availability for domestic and international travel.

Remote Clinical Trial Manager role in a precision medicine CRO responsible for site selection, start-up, enrollment management, monitoring planning/execution, data cleaning, regulatory documentation, and close-out across multiple countries (UK, Hungary, Poland, Romania, Serbia, Slovakia). Requires significant clinical trial management experience (oncology), working knowledge of ICH-GCP, and effective English communication. Role includes mentoring CRAs and cross-functional collaboration; domestic and international travel required.

Responsible for creating and executing TMF Plans and Indexes, ensuring timely document review/processing and periodic quality reviews, monitoring TMF health and metrics, supporting audits/inspections, managing eTMF activities and study close-out. Requires a Bachelor's degree (or equivalent) and a minimum of 3 years related experience; professional working proficiency in English.