Provide program-level leadership and operational oversight for assigned Functional Service Provider (FSP) projects, serving as primary operational contact for clients. Responsibilities include coordinating cross-functional activities, monitoring risks and quality trends, supporting financial oversight and forecasting, leading internal and client meetings, maintaining program processes/trackers, and contributing to onboarding and mentoring of FSP team members. Requires a bachelor’s degree (or equivalent), minimum 3–5 years clinical research experience with at least 2 years leading a project, strong knowledge of ICH-GCP and clinical trial systems, and proficiency with Microsoft Office.

Provide program-level leadership and operational oversight for assigned FSP projects, act as primary client operational contact, coordinate cross-functional deliverables, monitor risks/issues/quality, support financial oversight, and lead internal and client-facing meetings. Requires experience with clinical trial systems (EDC, eTMF, CTMS), strong knowledge of ICH-GCP and clinical operations, and proficiency in English.

Support country/site start-up and regulatory activities for clinical trials, including preparation and submission of dossiers to Competent Authorities and Ethics Committees, managing site activation readiness, maintaining TMF and project trackers, coordinating translations, assisting with IMP release and contract/budget negotiations, and ensuring compliance with ICH-GCP. Requires a bachelor's in life sciences or equivalent (or RN), fluency in English, and 1+ year regulatory or site start-up experience.

Lead development of investigator/site budgets during proposals, manage global investigator grant workbooks, oversee payment processing and reconciliations, contribute to month-end close, and manage Sunshine Act and client reporting. Requires a bachelor's degree, at least 5 years clinical research experience and 3+ years in a leadership role.

The Business Development Director (Biospecimen Solutions) is responsible for identifying, engaging, developing, and closing business opportunities for biospecimen products and services. The role requires account growth and retention, lead qualification, CRM management (Salesforce), cross-functional coordination, and up to 35% travel. Reported salary range: $162,000–$243,000 USD per year.

The Regulatory and Site Start Up Specialist prepares clinical trial application dossiers and amendments for Competent Authorities and Ethics Committees, customizes informed consent and patient information documents, manages collection and quality review of essential documents and TMF filing, coordinates translations, supports site contracts and budget negotiations, and works with CRAs and cross-functional teams to ensure timely site activation in compliance with local and international regulations (ICH-GCP). Based in China (remote).

The Project Support Specialist will support project teams in clinical trial operations, including maintaining project timelines (MS Project), CTMS activities, SharePoint sites, TMF documentation, meeting coordination and minutes, training records, user access, study supply management, and distribution/tracking of safety reports. Requires a 4-year degree or equivalent, minimum 2 years relevant experience (e.g., Clinical Trial Assistant), proficiency with Microsoft Office, and professional-level English; working knowledge of ICH-GCP and regulatory SOPs.

Provide cross-functional project support for clinical studies including maintaining project timelines (MS Project), CTMS updates, meeting scheduling and minutes, TMF and study binder preparation, training and user access management, study communications (e.g., SUSARs/IND reports), and coordination with vendors. Requires a 4-year degree (or equivalent) and a minimum of 2 years' relevant experience; English proficiency and working knowledge of ICH-GCP and SOPs are required.

Provides cross-functional operational and administrative support for clinical studies, including maintaining project timelines (MS Project), CTMS tasks, scheduling meetings and minutes, TMF and binder management, training records, user access, and study communications. Requires a 4-year degree (or equivalent) and a minimum of 2 years relevant experience; working knowledge of ICH-GCP and Microsoft Office is expected.

Provide cross-functional project support for clinical studies including maintaining project timelines (MS Project), CTMS tasks (milestones, contacts, enrolment projections), meeting scheduling and minutes, TMF and study binder management, training coordination and records, SharePoint site setup, user access and helpdesk ticketing, study supplies and shipping coordination, and support for safety report distribution (IND/SUSAR) as needed. Requires a 4-year degree or equivalent, minimum 2 years relevant experience (e.g., Clinical Trial Assistant), professional-level English, proficiency in Microsoft Office, and working knowledge of ICH-GCP and regulatory guidance.

Precision for Medicine seeks a Senior Manager/Manager, Global Clinical Monitoring (based remotely in Poland) to line-manage CRAs, IHCRAs and CTMs across multiple European countries, ensure high-quality clinical operations delivery, support resource planning, lead process improvement and workforce development initiatives, and perform site visits as required. Fluency in English and Polish and experience in CRO/biotech/pharma clinical operations and ICH-GCP are required. Travel up to ~25%.

The role leads development of high-quality, on-time clinical documents (protocols, IBs, ICFs, DSURs, CSRs, patient narratives) and manages document workflows with sponsors, vendors, and internal teams. Requires 5+ years' senior medical writing experience (or 7+ years as Principal), strong knowledge of ICH/FDA/GCP and eCTD, proficiency with Word/Excel/PowerPoint/Adobe/Teams, and excellent attention to detail and communication skills.

Precision for Medicine seeks an experienced Clinical Project Manager / Senior Clinical Project Manager to oversee full-service (Phase I–IV) oncology trials in a CRO environment. Responsibilities include project delivery across functional areas (data management, safety, clinical, medical monitoring, biostatistics), proposal and costing activities, client liaison, budget and timeline management, and cross-functional team leadership. Requires a life sciences degree (or equivalent), CRO full‑service project management experience (minimum 4 years), oncology trial experience, and working knowledge of GCP/ICH.

Lead and deliver global/regional phase I–IV oncology clinical trials in a full-service CRO setting, accountable for project scope, budget, timelines, quality and client relationship. Requires a life sciences degree (or equivalent), at least 4 years' full-service project management experience in clinical trials, CRO experience, knowledge of GCP/ICH, and proficiency with CTMS/eTMF/EDC/IXRS; travel availability required.

Lead and oversee full-service global/regional Phase I–IV oncology clinical trials within a CRO setting. Responsibilities include project delivery across functional areas (data management, safety, medical monitoring, biostatistics), proposal and budgeting activities, client liaison, and cross-functional team coordination. Requires a life sciences degree (or equivalent), at least 4 years full-service project management experience in clinical trials, Oncology experience, knowledge of GCP/ICH, and familiarity with CTMS, eTMF, EDC, IXRS and MS Project. Role requires domestic and international travel availability.

Lead and deliver full-service global/regional oncology clinical projects across all study stages (proposal, execution, closeout). Accountable for oversight of functional departments (data management, safety, clinical, medical monitoring, biostatistics), client relationship management, budgets and timelines. Requires a life-science degree or equivalent, at least 4 years full-service project management experience in a CRO, oncology experience, and working knowledge of GCP/ICH; willing to travel internationally.

Accountable for full-service oversight of global/regional Phase I–IV oncology trials including project delivery, cross-functional coordination (data management, safety, clinical, medical monitoring, biostatistics), proposal strategy and costing, client relationship management, budgets and timelines. Requires a life sciences degree or equivalent, at least 4 years' full-service project management experience in a CRO, knowledge of GCP/ICH, and experience with CTMS, eTMF, EDC and IXRS. Position is remote (Serbia) and requires domestic and international travel.

Precision for Medicine is hiring a Clinical Project Manager / Senior Clinical Project Manager to manage end-to-end (ph I-IV) Oncology trials in a CRO setting. Responsibilities include full-service project oversight, client liaison, proposal/costing activities, managing budgets and timelines, coordinating functional areas (data management, safety, clinical, medical monitoring, biostatistics), and preparing study documentation. Role requires at least 4 years' full-service project management experience in clinical trials and working knowledge of GCP/ICH.

Lead full‑service oversight of global/regional Phase I–IV oncology clinical trials for a CRO, accountable for project delivery, budgets, timelines, client relationships and cross‑functional coordination. Requires a life‑science degree (or equivalent), at least 4 years' full‑service project management experience in clinical trials within a CRO, knowledge of GCP/ICH, experience with CTMS/eTMF/EDC/IXRS, and availability for domestic and international travel.

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.