Seeking an experienced Project Director to oversee global or large oncology clinical studies and portfolios. Responsibilities include client liaison, project and financial management, quality and risk oversight (eTMF/ICH-GCP), mentoring project managers, supporting business development (bid defenses), and ensuring study execution across cross-functional teams. Position is fully remote from the UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia.

Hiring a Project Director to lead and oversee global or large oncology clinical studies or portfolios. Responsibilities include client liaison, project team leadership, budget and financial oversight, project planning, risk/change management, quality (eTMF) and regulatory compliance, mentoring project managers, and supporting bid defenses. Role is remote (UK, Spain, Poland, Hungary, Romania, Serbia or Slovakia) and requires ability to travel; candidates must be authorized to work without employer sponsorship.

Lead clinical trial operations for oncology and rare disease studies, ensuring compliance with protocol, SOPs and ICH-GCP. Responsibilities include site feasibility and start-up, CRA oversight and monitoring, eTMF and CTMS management, regulatory/IRB submissions, IP accountability, vendor management, training, and CAPA implementation. Position is remote in Australia and requires Mandarin proficiency and the ability to travel domestically and internationally.

First Senior Regulatory and Start-Up Specialist in Argentina supporting clinical trial submissions to Competent Authorities and IRB/ECs, informed consent adaptations, essential document collection, site activation readiness, and partnering with CRAs and Site Contract Management on budgets and contracts. Requires a bachelor's degree (or RN), fluency in English and the local language (Spanish), and 3.5+ years of relevant regulatory or site start-up experience; occasional travel may be required.

Lead development and optimization of clinical data systems and ETL pipelines for global trials across LATAM. Responsibilities include enterprise data standardization and mapping, designing validation frameworks, SAS-based modular codebases, database design and optimization, dashboarding, and ensuring regulatory compliance with GCP and FDA 21 CFR Part 11. Requires professional working proficiency in English and at least 6 years of relevant clinical trial/monitoring/management experience.

Precision for Medicine seeks a Regulatory and Start Up Specialist based in Spain to manage site activation readiness, prepare clinical trial application dossiers and submissions to competent authorities/ethics committees, and support contracts and budget negotiations. The role requires experience in regulatory or start-up functions within a CRO or pharma/biotech, strong communication and organizational skills, and fluency in English and Spanish. Responsibilities include maintaining project trackers and TMF, coordinating translations, liaising with CRAs and other functions, and ensuring compliance with ICH-GCP and local regulations.

Remote Senior CRA to support clinical studies across Brazil. Responsibilities include site start-up and feasibility, on-site and remote monitoring, ISF/TMF reconciliation, EDC/EHR data review, SAE reporting, investigational product oversight, regulatory/IRB submissions, mentoring junior staff, and preparing monitoring reports. Requires 5+ years as a CRA, a scientific/healthcare degree, professional-level English, and up to ~60% travel. Candidates must be authorized to work in the country of employment without employer sponsorship.

Precision For Medicine seeks a Senior Clinical Research Associate based in Chile (remote) to independently manage site start-up and monitoring activities, ensure patient safety and data quality, perform on-site and remote monitoring (including EDC/CRF review), support regulatory/IRB submissions, handle investigational product reconciliation, prepare monitoring reports, mentor junior staff, and travel up to ~60%. Requires a 4-year degree (or equivalent) and 5+ years as a CRA; English proficiency at a professional level is required. Candidates must be authorized to work in the country without employer sponsorship.

Precision for Medicine is hiring a Safety Specialist/Safety Lead to manage pharmacovigilance activities including safety management plan development, SAE/SUSAR case management (intake to regulatory reporting), ICSR composition, medical coding, QC, preparation/review of safety reporting and medical coding plans, and safety training. Role requires hands-on experience with global safety databases and familiarity with MedDRA, WHODrug, FDA regulations, and ICH guidelines. BA/BS and a minimum of 5 years of safety experience are required; nursing or pharmacy degree and Argus experience are preferred.

Precision for Medicine seeks a Senior Feasibility Associate or Feasibility Manager (title depends on experience) to perform clinical-trial feasibility analyses across pre-award, post-award, rescue, and standalone engagements. The role involves protocol review, epidemiology and site analyses, recruitment forecasting, collaboration with cross-functional teams and clients, and contributing to feasibility methods and tools. Position can be fully remote in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.

Precision for Medicine seeks a Feasibility Manager / Senior Feasibility Associate to deliver evidence-based feasibility assessments for global clinical trials. The role involves clinical and epidemiological interpretation, site and country analyses, recruitment forecasting, stakeholder engagement, and presenting recommendations. Remote coverage is allowed in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia. Candidates must be legally authorized to work without employer sponsorship.

Precision for Medicine seeks a Senior Feasibility Associate or Feasibility Manager to deliver evidence-based feasibility assessments (pre/post-award, rescue, stand-alone) for global clinical trials. Responsibilities include protocol review, epidemiology and site analyses, recruitment and operational recommendations, stakeholder presentations, and development of feasibility methods. Requires a bachelor's in life sciences (or related), at least 2 years' relevant experience, professional proficiency in English, and working knowledge of ICH-GCP. The role can be covered remotely in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia.

Precision for Medicine is hiring a Senior Feasibility Associate or Feasibility Manager (title based on experience) to deliver evidence-based feasibility assessments across pre-award, post-award, rescue, and stand-alone engagements. The role includes protocol review, epidemiology and site/patient-pool analyses, recruitment recommendations, stakeholder presentations, and collaboration across Business Development, Clinical Operations, and Medical teams. Position can be fully remote in the listed European countries; candidates must be legally authorized to work in the country of employment without employer sponsorship.

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 is hiring a Senior Feasibility Associate/Feasibility Manager to deliver evidence-based feasibility assessments across pre-award, post-award, rescue, and standalone engagements. Requires a bachelor's in life sciences or related field, at least 2 years relevant experience (feasibility, clinical operations, epidemiology, or similar), and professional proficiency in English. Role can be fully remote in the UK, Spain, Hungary, Poland, Romania, Serbia, or Slovakia; candidates must be legally authorized to work in the country of employment without employer sponsorship.

Responsible for conducting and presenting feasibility assessments (country, site, patient-pool, recruitment) across pre-award, post-award, rescue and standalone engagements; reviewing protocols and study assumptions; coordinating site/investigator outreach; collaborating with Business Development, Clinical Operations and other stakeholders. Requires a life-sciences bachelor's degree, professional English, and at least 2 years' relevant experience; knowledge of ICH-GCP and proficiency with Excel/PowerPoint/Word and web-based data platforms preferred.

The Regulatory Manager provides regulatory development advice and coordinates preparation of regulatory documents and submissions (including IND/CTA, amendments, annual reports, scientific advice, orphan and pediatric filings) to Regulatory Authorities and Ethics Committees. The role supports regulatory strategy, maintains regulatory intelligence and project trackers, oversees Regulatory Affairs Specialists as needed, provides ICH GCP guidance, and requires 5+ years of relevant regulatory affairs experience. Position is remote (United States) and requires availability for domestic and international travel.

Provides leadership and strategic direction for the Site Start-up (SSU) department, ensuring execution of SSU activities (e.g., informed consent adaptation, regulatory document collection and review, IRB/EC/CA submissions, and support for site contracts and budgets). Oversees large and complex SSU programs, drives process optimization and KPIs, partners with cross-functional teams, and supports team development and resourcing. Requires a minimum of 12 years in clinical research and fluency in English.

Responsible for end-to-end site start-up strategy and execution including ICF customization, IRB/EC and CA/MoH submissions, IMP release packaging, milestone planning and tracking, stakeholder coordination, translations, and mentoring staff. Requires a bachelor's degree or RN, 5+ years' start-up experience (CRO/pharma/biotech preferred), project milestone management experience, fluency in English and local language where applicable, and legal authorization to work without employer sponsorship.

Precision For Medicine seeks a Start Up Specialist (open to levels with site start-up experience from a CRO) to prepare clinical trial application dossiers, manage CA/EC submissions and interactions, maintain project trackers and TMF, support site activation (including IMP release and ICF customization), coordinate translations, and liaise with feasibility, clinical operations and contracts teams. Candidates must be fluent in Hungarian and English and legally authorized to work in the country of employment without employer sponsorship. Candidates located in Hungary, Poland, Serbia, Slovakia or Romania are eligible.