Lead clinical operations for studies across Latin America, serving as primary client contact and owning feasibility, site start-up, monitoring, eTMF, regulatory/IRB submissions, recruitment strategies, vendor and budget coordination, CRA mentoring, and quality/CAPA activities. Remote role covering Mexico, Brazil, Argentina, Colombia, Chile, and Peru; requires at least 7 years' clinical research experience and professional working proficiency in English. Travel domestically and internationally is required.

Senior/CRA responsible for independently overseeing study site management, start-up activities, on-site/remote monitoring (pre-study, initiation, routine, close-out), preparing monitoring reports, ensuring GCP and regulatory compliance, reconciling ISF/TMF, assisting with IRB/EC submissions, IP management, SAE processing, and mentoring junior staff. Minimum ~3.5 years on-site monitoring experience, oncology and global clinical trial experience required. Role is remote based in Hong Kong and requires frequent travel (60–70%).

Remote (United States) Senior Project Manager role leading oncology clinical trials. Responsible for study planning and execution, budget and profitability oversight, vendor and cross-functional coordination, quality/eTMF readiness, risk mitigation, and client/stakeholder communication. Requires minimum 7 years of clinical research experience (and at least 4 years direct project management), with international travel as needed.

Responsible for creating and explaining change order budgets, performing variance and financial analysis, maintaining change order records/metrics, preparing change order documents, and coordinating with project teams, vendors and clients. Requires a bachelor’s degree (or equivalent), a minimum of 5 years’ experience in change order/proposal preparation using Excel-based costing tools, strong financial and Excel skills; CRO experience and MBA are preferred. Minimal travel.

Precision for Medicine seeks a Regulatory and Site Start Up Specialist to manage clinical trial submissions to Competent Authorities and IRB/ECs, adapt informed consent forms, collect and review essential documents, support site activation and IMP release, and assist with site contract and budget negotiations. The role requires at least 1 year of relevant experience, fluency in English, knowledge of ICH-GCP, and the ability to use standard electronic office systems and tracking tools.

Senior Director in Scientific Affairs for Specialty Lab Services (remote, US) responsible for leading a Scientific Affairs team, owning global third-party lab and 3PL relationships, supporting RFPs/BDMs and proposal development, performing operational and protocol analysis, developing budgets and assay specifications, mentoring staff, and representing the company in client and industry forums. Requires 15+ years in the CRO/lab industry; PhD preferred.

Principal/Senior-level role focused on clinical and indication-specific data review, eCRF/EDC guidance, RBQM support, and cross-functional collaboration for oncology (required), rare disease, and autoimmune studies. Requires a minimum of 8 years clinical research experience, at least 3 years oncology experience (within the past 1.5 years), and a minimum of 1 year leadership experience. Remote role available in specified countries; occasional domestic and international travel (~up to 25%). Candidates must be authorized to work in the country of employment without employer sponsorship.

The Senior Principal Technical Data Specialist will define and govern enterprise technical data expectations across clinical programs in Latin America, oversee database design and EDC platform architecture, lead testing/validation and migration/archival practices, and drive integration, interoperability and AI enablement. The role is remote for Argentina, Brazil, Colombia, Mexico (and the description also references Chile and Peru) and typically requires 12+ years of relevant experience.

Manage and mentor financial analysts; design and implement project financial processes; produce monthly financial metrics (revenue recognition, forecasting, variance analysis, project utilization, consultant/vendor spend); support project teams running clinical trials; perform invoicing support, EVA, contract and change order review; liaise with intercompany finance teams and act as financial lead in project reviews and QBRs. Minimum eight years project finance experience and CRO industry experience; occasional travel required.

Responsible for independent, risk-based Quality Assurance oversight of GxP computerized systems throughout the system lifecycle (assessment, validation, operation, change, and retirement). Reviews and approves validation deliverables, supports vendor qualification and audits/inspections, develops CSV/CSA policies and training, and drives continuous improvement. Requires a bachelor’s degree (or equivalent) and a minimum of six years' relevant experience. Location: Remote, United States.

Join Precision as a Start Up Specialist responsible for preparing Clinical Trial Applications and submission dossiers, interacting with Competent Authorities and Ethics Committees, maintaining project plans/trackers, coordinating translations and essential document collection, supporting IMP release and TMF maintenance, and assisting with feasibility, budget negotiation and investigator contracts. Candidates must be fluent in Hungarian and English. Open to applicants in Hungary, Poland, Serbia, Slovakia or Romania; candidates must be legally authorized to work in the country of employment without employer sponsorship.

Remote Start Up Specialist role supporting preparation and submission of clinical trial applications and dossiers to Competent Authorities and Ethics Committees, coordinating site activation (including IMP release and essential documents), managing translations, liaising with CRAs and cross-functional teams, and maintaining TMF and regulatory trackers. Candidates must be fluent in Hungarian and English and may be located in Hungary, Poland, Serbia, Slovakia or Romania.

Precision For Medicine is hiring a Start Up Specialist to prepare and submit clinical trial application dossiers, interact with Competent Authorities and Ethics Committees, maintain project plans/trackers and support site activation (including IMP release, essential documents, ICF customization and translations). Role requires fluency in Hungarian and English and experience in site start-up or regulatory/start-up roles within a CRO or pharma/biotech. Candidates located in Hungary, Poland, Serbia, Slovakia or Romania are eligible; employer will not sponsor work visas.

Precision for Medicine seeks a Clinical Trial Manager to manage clinical aspects of multi-country oncology trials (site selection, start-up, enrolment, monitoring, data cleaning, close-out), lead CRAs, ensure regulatory documentation and quality delivery, and mentor team members. Candidates may work remotely in Hungary, Poland, Romania, Serbia, or Slovakia. English communication and availability for domestic/international travel are required. Visa sponsorship is not provided.

Precision for Medicine seeks an experienced Clinical Trial Manager to lead clinical aspects of multinational oncology trials, oversee CRAs, manage site selection/start-up/enrolment/monitoring/data cleaning/close-out, and ensure GCP/ICH-compliant delivery. Candidates must be able to work remotely from Hungary, Poland, Romania, Serbia or Slovakia, communicate effectively in English, be available for domestic and international travel, and not require employer visa sponsorship.

Experienced Clinical Trial Manager to manage clinical elements of trials across multiple countries within a CRO, with focus on oncology and precision medicine. Responsibilities include site selection and start-up, enrolment management, monitoring planning and execution, data cleaning, close-out, mentoring CRAs, and ensuring regulatory/GCP compliance. Requires strong CRO/pharma clinical lead experience and effective English communication.

Precision for Medicine seeks a Clinical Trial Manager to lead clinical aspects of multi-country oncology studies, managing site selection, start-up, enrollment, monitoring, data cleaning and close-out. The role requires experience in CRO/pharma clinical lead roles, knowledge of ICH-GCP, familiarity with CTMS/eTMF/EDC/IXRS tools, and the ability to travel domestically and internationally.

Precision for Medicine seeks an experienced Clinical Trial Manager to manage clinical elements of multi-country oncology trials (site selection, start-up, monitoring, enrolment, data cleaning, close-out), lead CRAs, maintain regulatory documentation, and ensure timeline adherence and quality. Requires demonstrated multi-country clinical lead experience in a CRO/Pharma/Biotech, working knowledge of ICH-GCP, English proficiency, and availability for domestic/international travel. Experience with CAR-T and radiopharmaceuticals is a strong plus.

Lead data manager for assigned clinical projects overseeing database development, UAT, edit checks, data entry quality, queries, medical coding, SAE/AE reconciliation, TMF documentation and vendor interactions. Requires experience with EDC systems, database migrations, SOPs, and prior Clinical Data Manager or Senior Clinical Data Manager experience (5+ years as CDM II or 8+ years as Sr. CDM). Oncology experience preferred.

Hiring a Senior Clinical Data Manager (or Clinical Data Manager II) to manage all aspects of clinical trial data management from study start-up through post-database lock, including CRF specifications, database build and UAT, edit checks, medical coding, SAE/AE reconciliation and vendor coordination. Role is remote with candidates considered in Poland, Hungary, Romania, Serbia, Slovakia and the United Kingdom; requires professional English and 5–8+ years of relevant experience (8+ years as Sr. CDM or 5+ years as CDM II).