Precision for Medicine is hiring a Clinical Research Associate II (remote) for candidates based in Belgium or the Netherlands. Role focuses on monitoring oncology clinical trials, site management, study start-up and regulatory activities, ensuring compliance with protocol, SOPs and ICH-GCP. Requires a life sciences degree or equivalent and a minimum of 2 years CRA experience; fluency in English is required, Dutch and French are a plus. Travel (including overnight stays) may be up to ~50–60%.

Precision for Medicine is seeking a CRA II (remote) based in Belgium or the Netherlands to monitor oncology clinical studies, perform site management and study start-up activities, and ensure compliance with protocol, SOPs, and ICH-GCP. The role requires approximately 50-60% travel and a minimum of 2 years CRA experience.

Lead biostatistician responsible for authoring and reviewing statistical protocol sections and SAPs, generating analysis datasets/tables/figures using SAS, performing sample size and adaptive design calculations, supporting DMC reports and regulatory submissions, and providing biostatistical consultation to sponsors and internal teams. Requires advanced knowledge of ICH, CDISC, FDA/21 CFR Part 11, and substantial clinical trial experience (Master's +10 years or PhD +7 years). Candidates must be legally authorized to work in the country of employment without employer sponsorship.

The Clinical Trial Manager leads operational aspects of clinical studies (site feasibility, start-up, monitoring, vendor and IP management, eTMF, CTMS and data quality) ensuring compliance with protocol, SOPs, ICH-GCP and regulatory/IRB requirements. Requires a bachelor's (advanced degree preferred), 5–8 years clinical research experience including Phase 1 FIH and healthy volunteer trials, Mandarin proficiency and ability to travel internationally. Remote positions for Australia, Singapore and South Korea.

Precision for Medicine seeks a home-based CRA II / Senior CRA in Poland to independently manage and monitor investigative sites for oncology studies (including potential Phase I/CAR-T experience). The role requires 3+ years of independent monitoring experience, fluency in Polish and English, adherence to ICH-GCP/SOPs, and availability for domestic travel (approximately 50–60%) with occasional international travel.

The Site Contracts Manager will support the European team remotely (eligible from Poland, Slovakia, Serbia, Romania or Hungary) by drafting, reviewing, negotiating and tracking clinical study agreements, site contracts, vendor agreements and related documents; collaborating with clinical operations and stakeholders to meet study timelines; maintaining contract files and metrics; and helping design contracting policies and procedures. Minimum requirements include a 4-year degree and at least 5 years relevant CRO/healthcare contract experience.

Precision for Medicine seeks a Site Contracts Manager to support Clinical Operations by drafting, reviewing, negotiating and tracking CTAs, MSAs, vendor agreements and site budgets. The role requires a minimum of 5 years' CRO/healthcare experience, experience leading study team interactions, and can be performed remotely from Poland, Slovakia, Serbia, Romania or Hungary; candidates must be legally authorized to work without employer sponsorship.

Precision for Medicine seeks a Site Contracts Manager (remote from Poland, Slovakia, Serbia, Romania or Hungary) to review, draft, negotiate and track site clinical trial agreements, vendor agreements and related contracts. Requires minimum 5 years' relevant CRO/healthcare contracting experience, collaboration with clinical operations and management of contract metrics, files and processes.

Precision for Medicine seeks a Site Contracts Manager (manager-level) to review, draft, negotiate and manage clinical study-related agreements (CTAs, MSAs, vendor and confidentiality agreements), track contract metrics, maintain contract files, and coordinate with Clinical Operations and study teams. Requires a 4-year degree and at least 5 years' relevant CRO/healthcare contracting experience. Candidates must be authorized to work in the country of employment without employer sponsorship.

Precision for Medicine is hiring a Site Contracts Manager to work fully remotely from Poland, Slovakia, Serbia, Romania or Hungary. Responsibilities include drafting, reviewing, negotiating and managing site clinical trial agreements, vendor contracts and site budgets; liaising with clinical operations and sponsors; maintaining contract files and metrics; and improving contracting processes. Minimum 5 years' relevant CRO/healthcare contracting experience required.

Lead and deliver full-service clinical oncology trials within a CRO setting, accountable for project delivery across clinical, data, safety and biostatistics functions. Responsibilities include proposal development, budget and timeline management, client liaison, protocol and study documentation oversight, and international travel as required. Requires at least 4 years' full-service project management experience and knowledge of GCP/ICH.

Lead and deliver full‑service oncology clinical trials within a CRO environment, overseeing clinical operations, data, safety, medical monitoring and biostatistics. Accountable for study lifecycle activities including proposals, costing, protocol and study documentation, budget and timeline management, client liaison and cross‑functional team coordination. Requires a life‑science qualification (or equivalent), at least 4 years' full‑service project management experience in clinical trials, oncology experience, GCP/ICH knowledge, and proficiency in English.

Lead full-service clinical projects in Oncology across all study stages (proposal, execution, closeout). Accountable for project delivery, budget, timelines, client relationship and cross-functional oversight (data management, safety, clinical, medical monitoring, biostatistics). Role based remotely (Poland) with domestic and international travel.

Lead and deliver global/regional Oncology clinical trials (Phase I-IV) in a full-service CRO setting. Accountable for project oversight across functions (data management, safety, clinical, medical monitoring, biostatistics), proposal and costing activities, client liaison, and ensuring timelines, scope, cost and quality. Requires a life sciences degree (or equivalent), at least 4 years' full-service project management experience in a CRO, Oncology trial experience, knowledge of GCP/ICH, and availability for domestic and international travel.

Precision for Medicine seeks a Senior Clinical Project Manager (Oncology) to lead end-to-end clinical trials (Ph I–IV) in a CRO setting. Responsibilities include full-service oversight across functional areas (data management, safety, clinical, medical monitoring, biostatistics), proposal and costing participation, client liaison, team coordination and ensuring study delivery to agreed scope, timelines and budget. Role requires at least 4 years of full-service project management experience in clinical trials and strong knowledge of GCP/ICH.

Senior Clinical Project Manager responsible for end-to-end management of global/regional Phase I-IV oncology trials within a CRO setting. Accountable for project delivery, oversight of functional areas (data management, safety, clinical, medical monitoring, biostatistics), client liaison, proposal activities, budgets and timelines. Requires at least 4 years full-service project management experience in clinical trials and strong knowledge of GCP/ICH.

Lead and deliver full-service oncology clinical projects across global/regional Phase I–IV trials, accountable for timelines, scope, budget and quality. Manage cross-functional teams (data management, safety, clinical, medical monitoring, biostatistics), client relationships, proposal activities and study documentation. Remote role based in Spain; requires experience in CRO full-service project management, working knowledge of GCP/ICH, strong communication and presentation skills, and availability for domestic and international travel.

Responsible for supporting clinical project teams on financial activities (invoicing, revenue recognition, variance analysis, project budgets, change orders) and assisting company accountant with general ledger, financial reporting and month/quarter/year-end close. Requires a bachelor’s in accounting/finance (preferred MBA/CPA), minimum 5 years relevant experience, proficiency with QuickBooks and Excel, and occasional domestic/international travel.

Lead a team within Operational Strategy to develop operational approaches for RFPs, bid-defense meetings, feasibility and site recommendations, budgeting, and transition to delivery. Requires extensive CRO/pharmaceutical experience (approximately 18 years), strong analytical, budgeting and leadership skills, ICH-GCP knowledge, and willingness to travel domestically and internationally.

Senior People Operations Partner (based in Mexico) providing advanced multi-country HR operational leadership across Mexico, Brazil, Argentina, Colombia, Chile, and Peru. Responsibilities include complex employee relations, legislative compliance, works council/employee representative processes, organizational change and restructures, operational governance, HR process and technology improvements, and partnering with HRBPs, Legal, Payroll and business leaders to ensure compliant, scalable HR operations.