Precision for Medicine is seeking a Site Contracts Manager to review, draft, negotiate and track clinical trial agreements, confidentiality agreements and vendor contracts across APAC. The role works closely with Clinical Operations and study teams, is client-facing during site contracting, and requires setting up contracting strategies and managing site budget negotiations. Requires minimum 5 years' relevant experience, tertiary qualification (or equivalent), CRO/life-science experience and fluency in English. Some domestic and occasional international travel is required.

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.

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.

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.

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.

Role involves reviewing, drafting, negotiating and tracking site Clinical Trial Agreements, vendor and other client contracts; coordinating with Clinical Operations and study teams to meet timelines; maintaining contract files and metrics; and contributing to contracting policies and process improvements. Requires a 4-year degree and at least 5 years' relevant experience in CRO/healthcare contracting.

The Senior Clinical Data Manager leads data management activities from study start-up to post-database lock for assigned clinical projects, including CRF specifications, database build and UAT, edit checks, query management, medical coding (MedDRA/WHODrug), SAE/AE reconciliation, TMF documentation, vendor coordination and team training. Requires 8+ years' experience, professional English, and experience with EDC systems (Medidata Rave, Veeva); occasional travel may be required.