The Finance and Systems Coordinator is responsible for maintaining financial systems focused on project time and expense: administering timesheets, managing the time and expense helpdesk, adding/removing staff from projects, training and onboarding users, correcting timesheets and assisting with large-scale adjustments, and delivering scheduled and ad-hoc reporting. Requires a high school diploma (Bachelor's preferred), a minimum of three years' administrative experience, strong Excel/Microsoft Office skills, and attention to detail.

Lead CDx regulatory strategy and consulting engagements for pharmaceutical, biotech, and diagnostic clients, translating FDA, EU IVDR, and other global requirements into actionable development, clinical-trial, submission, and commercialization plans. Responsibilities include preparing and directing global regulatory submissions (e.g., Q-Subs, IDEs, PMAs, EU IVDR performance study applications), advising on analytical and clinical validation, coordinating cross-functional teams, and supporting business development and client workshops.

Lead delivery of oncology clinical trials as primary client point of contact and escalation, coordinating internal functions and external vendors, managing study budgets and profitability, ensuring quality (eTMF/inspection readiness), developing project plans and risk mitigations. Requires minimum 7 years clinical research experience and at least 4 years direct project management experience; radiopharmaceutical and cell/gene therapy experience preferred.

Lead clinical operations across LATAM (Mexico, Brazil, Argentina, Colombia, Chile, Peru). Own planning, execution and oversight of studies as primary clinical contact; develop recruitment strategies, lead feasibility and site start‑up, implement monitoring and quality strategies, manage eTMF/CTMS, support regulatory/IRB submissions, mentor CRAs and manage vendors. Minimum 7 years clinical research experience and professional working proficiency in English; role requires domestic and international travel.

Responsible for gathering and analysing competitive and market information, identifying and qualifying inbound leads, outbound prospecting, developing outreach plans, coordinating with marketing for collateral, maintaining CRM and sales enablement systems, and reporting activity to business development leadership. Requires familiarity with CRO/specialty labs markets and direct B2B sales experience; English fluency and willingness to travel are required.

Precision for Medicine seeks a Clinical Research Associate II (home based in the UK/Northern Ireland) to own site-level monitoring and study progress, coordinate study setup activities (investigator identification, regulatory support, pre-study/initiation visits), and ensure studies are conducted per protocol, SOPs and ICH-GCP. Candidate should have a 4-year degree (or equivalent), ideally >1 year CRA experience; oncology and early phase experience desirable. Role requires domestic travel up to approximately 50-60% (overnight stays).

The Senior Finance Analyst – Clinical Solutions Portfolio delivers portfolio-level financial analysis and project financial oversight across the project lifecycle, focusing on forecast accuracy, budget health, variance analysis, risk identification, and linking trial operations KPIs to financial outcomes. Requires ~5+ years' related experience, advanced Excel and Power BI skills, and experience in project finance or FP&A—preferably within a CRO/clinical research environment.

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.

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.

Remote senior-level role providing project finance support and accounting functions: project budgets, invoicing, revenue recognition, variance and Earned Value Analyses, change order review, month-end close and general ledger/financial reporting. Requires 5+ years relevant experience and fluency in English plus the local language for the country of work.

Lead clinical trial activities including site feasibility and start-up, CRA oversight, eTMF and CTMS management, IP accountability, regulatory/IRB submissions, development of clinical documents and training, vendor and budget oversight, CAPA implementation, and cross-functional coordination. Requires a bachelor’s (advanced degree preferred) and a minimum of 5 years clinical research experience; regional experience covering China market and oncology experience preferred.

Responsible for supporting training strategy and delivering instructor-led, virtual, and e-learning programs across translational sciences, clinical operations, project management, data management, and regulatory/compliance. Acts as intake point for training requests, coordinates new-hire onboarding, manages learning platforms and training records, and partners with SMEs to maintain role-based curricula. Requires 4+ years L&D experience supporting CRO delivery teams and strong knowledge of ICH/GCP.

Responsible for partnering with subject matter experts to assess training needs, design and deliver instructor-led, virtual, and e-learning programs, coordinate new-hire role-specific onboarding, manage learning platforms/LMS, maintain training documentation and reporting, and ensure training aligns with ICH/GCP and regulatory expectations. Requires a scientific/healthcare degree, ~4+ years L&D experience supporting CRO or clinical delivery teams, and proficiency with learning platforms and Microsoft Office.

Hiring a Manager, Learning & Development to assess training needs, design and deliver instructor-led, virtual and e-learning programs, coordinate new-hire onboarding, manage learning platforms, and maintain regulatory training records. Role supports clinical operations, translational sciences, project management, data management and regulatory/GCP areas; requires experience supporting CRO delivery teams and familiarity with ICH/GCP.

The Manager, Learning & Development will partner with subject matter experts to assess training needs and deliver instructor-led, virtual, and e-learning programs across translational sciences, clinical operations, project management, data management, and regulatory/GCP areas. Responsibilities include new-hire onboarding, intake and triage of training requests, managing learning platforms and documentation, and maintaining role-based curricula. Requires a scientific or healthcare degree, ~4+ years L&D experience (CRO experience preferred), proficiency with learning platforms and Microsoft Office, strong English communication, and knowledge of ICH/GCP and clinical trial activities.

Responsible for assessing training needs, designing and delivering instructor-led, virtual, and e-learning programs, coordinating new-hire role-specific onboarding, triaging training requests, and managing learning platforms and training documentation. Requires a scientific or healthcare background, 4–6 years L&D experience (CRO experience specified), proficiency with learning platforms and Microsoft Office, and strong communication, recordkeeping, and knowledge of ICH/GCP and clinical trial activities. Provided Poland salary range: 157,200 PLN–235,800 PLN gross per year.

Hire for a Senior Clinical Data Manager based in Mexico (remote). Responsible for leading clinical data management from study start-up through post-database lock, including CRF specification, database build and UAT, edit checks, medical coding (MedDRA/WHODrug), CDISC standards, SAE/AE reconciliation, vendor coordination, documentation (TMF/SOPs), reporting, and training. Requires 8+ years' experience and professional-level English.

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 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.