Responsible for end-to-end clinical data management from study start-up to post-database lock for assigned projects, including CRF specifications, database build and UAT, edit check development, medical coding, SAE/AE reconciliation, data reporting, vendor coordination and documentation. Requires professional English and a minimum of 5 years' relevant experience (5+ years as Clinical Data Manager II or 8+ years as Senior Clinical Data Manager). Oncology and database migration experience preferred. Remote; candidates in UK, Poland, Hungary, Romania, Serbia or Slovakia may be considered.

The Investigator Grants Associate II provides grant administration and financial support to project and finance teams, focusing on site payment tracking, CTA review, advance balance tracking, reconciliations, and relevant reporting (e.g., Sunshine Act, MMSE). Requires ~3 years clinical research experience, accounts payable background, and professional English proficiency.

The role manages all aspects of clinical trial data management from study start-up to post-database lock for assigned projects, including CRF specification, database build and UAT, edit check development, medical coding (MedDRA, WHODrug), query management, and SAE/AE reconciliation. The position is 100% remote (preference for east coast Canada) and requires leadership, training of project teams, vendor coordination, and occasional travel.

Manage all aspects of clinical trial data management from startup through post-database lock: CRF specifications, database build and UAT, edit checks, medical coding, query management, SAE/AE reconciliation, TMF documentation, vendor coordination, reporting, training, and support for protocols/SAPs/CSRs. Role is fully remote with occasional travel and an east-coast preference.

Manager for Site Start Up (APAC) overseeing Site Start Up (SSU) staff: hire, mentor, manage resources and FTE allocation, ensure compliance with SOPs and GCP/ICH, develop training plans, support onboarding, participate in resourcing and budgeting, and serve as SME for site start-up activities. Requires a bachelor’s in life sciences (or equivalent), a minimum of 6 years' clinical research experience with extensive site start-up experience and line management experience. Occasional travel may be required.

Responsible for managing and delivering pre-award, post-award, rescue, and stand-alone feasibility projects for clinical trials. Duties include detailed feasibility analyses (competitive, epidemiology, standards of care, drug), enrollment modeling, site outreach and identification, training and managing feasibility teams, presenting strategies to sponsors/clients, and supporting SOP/process development. Role requires a minimum of 7 years' related experience and professional-level English; remote in the United States with up to 10% travel.

Director-level regulatory consultant (remote, United States) responsible for designing regulatory and commercialization strategies for IVD/CDx products, directing preparation of global regulatory submissions, developing clinical and analytical protocols and technical reports, advising on quality systems and post-market requirements, leading business development activities, and managing staff and project teams. Minimum qualifications include a Bachelor's in Life Sciences and multi-year consulting experience (5–7+ years indicated).

Lead full-service clinical projects in Oncology within a CRO setting, overseeing all functional areas (data management, safety, clinical, medical monitoring, biostatistics). Accountable for project delivery, client liaison, proposals and budgeting, protocol and study documentation, and ensuring timelines, scope, cost and quality. Requires degree in life sciences or equivalent, 5+ years industry experience (minimum 4 years full-service PM), working knowledge of GCP/ICH, and availability for domestic and international travel.

Lead full-service clinical projects (Ph I-IV) in oncology within a CRO environment. Accountable for project delivery across functions (data management, safety, clinical, medical monitoring, biostatistics), proposal development, budgeting, client liaison, and international study execution. Requires a life science degree (or equivalent), 5+ years industry experience, at least 4 years full-service project management in a CRO, oncology experience, and working knowledge of GCP/ICH. Proficiency with CTMS, eTMF, EDC, IXRS and MS Office/Project is specified.

Accountable for end-to-end delivery of global/regional oncology clinical studies including proposal strategy, costing, bid defence, project planning and oversight of functions (data management, safety, clinical, medical monitoring, biostatistics). Requires 5+ years industry experience, at least 4 years full-service project management in clinical trials, working knowledge of GCP/ICH, and willingness to travel internationally.

Precision for Medicine seeks an experienced Clinical Project Manager (Senior) with 5+ years industry experience and at least 4 years full-service project management in a CRO. The role provides end-to-end oversight of global/regional Phase I–IV oncology trials, including proposal development, study execution, cross-functional coordination (data management, safety, clinical, biostatistics), client liaison, budgeting and travel for domestic/international studies. Required: life-science degree (or equivalent), GCP/ICH understanding, strong communication and presentation skills, and familiarity with CTMS, eTMF, EDC and IXRS.

Precision for Medicine seeks an experienced Senior Clinical Project Manager with 5+ years industry experience (at least 4 years full-service PM) to oversee global/regional phase I–IV oncology trials in a CRO setting. Responsibilities include full project oversight across functional areas (data management, safety, clinical, medical monitoring, biostatistics), proposal and protocol development, budget and timeline management, client liaison, and team coordination. Strong knowledge of GCP/ICH, experience with CTMS/eTMF/EDC/IXRS, and availability for domestic and international travel are required.

Precision for Medicine seeks a Senior Clinical Project Manager with 5+ years industry experience and at least 4 years full-service project management in a CRO to lead global/regional Oncology clinical trials (phase I–IV). Responsibilities include end-to-end project oversight, budgeting, stakeholder and client management, coordination of cross-functional teams, proposal development, and ensuring compliance with GCP/ICH. Remote role based in Poland with domestic and international travel expected.

Lead and oversee full-service global/regional Phase I–IV oncology clinical trials, accountable for project delivery, cross-functional team oversight, budgets, timelines and client communications. Requires 5+ years industry experience (minimum 4 years full-service project management), CRO experience, oncology trial experience, and knowledge of GCP/ICH; travel internationally as required.

Remote role based in Mexico supporting clinical data management across LATAM (Mexico, Brazil, Argentina, Colombia, Chile, Peru). Accountable for planning, implementation and oversight of DM activities (EDC, CRF specs, database build, UAT, edit checks), staff management, vendor coordination, SOP/process development, and ensuring data quality and timelines. Requires minimum 8 years of DM experience, 3 years of line management experience, and professional English.

Clinical Research Associate II (remote; must reside in Texas or California) responsible for study start-up, on-site and remote monitoring, ISF/TMF reconciliation, SAE reporting, IP management, EDC/EHR data review, and site management for clinical trials (including oncology). Requires a 4-year degree or equivalent and a minimum of 2 years as a CRA. Role involves up to ~60% travel. Salary range disclosed: $91,500–$137,300 USD/year.

The role leads the Clinical Operations department (trial management and monitoring) for projects in South Korea, ensuring compliance with ICH-GCP, FDA and company SOPs. Responsibilities include staffing and managing CRAs, coordinating internal and external project teams, contributing to SOPs, budgets and proposals, and serving as primary client interface for full-service complex trials. A minimum of 10 years' clinical research experience and strong communication, organizational and leadership skills are required.

Precision For Medicine is seeking a Senior Project Manager (Oncology) to plan, direct, coordinate and deliver clinical study projects. Responsibilities include client liaison, vendor coordination, budget and profitability management, development of project plans, quality and eTMF oversight, risk mitigation, reporting to clients and senior management, and leading cross-functional teams. Requires minimum 7 years clinical research experience (and minimum 4 years direct project management), familiarity with ICH-GCP, and experience with Microsoft Office, Microsoft Project, eTMF, EDC and CTMS. Oncology and cell/gene therapy experience preferred.

The Senior Feasibility Associate conducts global feasibility analyses and site identification for clinical trials (pre-award and post-award), supports RFP responses, recruitment and epidemiology analyses, site outreach, and enrollment modeling. Requires a life sciences bachelor’s degree, minimum 5 years' related experience, English professional proficiency, ICH-GCP knowledge, and willingness to travel domestically and internationally.

Lead medical writing for clinical study documents from template to final approved versions, collaborating with sponsors, vendors, and internal teams. Tasks include document planning, authoring complex content, editing/formatting, QC review, literature research, and contributing to SOPs/templates. Requires BS or equivalent in a scientific/medical discipline, 5+ years' sponsor/CRO medical writing experience, proficiency with Word/Excel/PowerPoint/Adobe/Teams, and knowledge of ICH/FDA/GCP/eCTD and clinical trial transparency; advanced degree and oncology/rare disease experience are preferred. Salary range disclosed: $100,600–$151,000 USD/year.