Lead end-to-end management of Precision For Medicine's global R&D tax credit and innovation incentive programs, including strategy, compliance, audit readiness, documentation, external advisor management, and global expansion. Drive financial analysis, KPI/reporting and business intelligence initiatives, partner with cross-functional stakeholders, and support analytics and transformation efforts. Requires a bachelor’s degree and 7+ years relevant experience.

Lead and manage central laboratory projects from conception to close-out, coordinating assay development, clinical testing, biorepository/sample management, logistics and kitting. Responsible for project planning, timelines, budgets, risk mitigation, client/vendor communication, reporting, and mentoring junior PMs. Role is remote (eligible in Poland, Serbia, Romania, Hungary, Slovakia, or the UK) and requires English fluency and international/domestic travel (~10–25%).

Lead and manage central laboratory projects across assay development, clinical testing, biorepository/sample management, logistics and kitting. Accountable for project planning/execution, risk and budget control, client/stakeholder communication, metrics/reporting, and mentoring junior PMs. Requires experience as a Project Manager for Central Laboratories and fluent English.

Leads central laboratory projects for CROs, pharma or biotech from conception through close-out, managing timelines, budgets, risk, and client relationships. Works remotely across specified European countries, coordinates assay development, biorepository/sample management, logistics/kitting, ensures regulatory compliance, and mentors junior project managers; travel ~10–25%.

Precision for Medicine is hiring a remote Project Manager for Central Laboratory Services to lead CRO laboratory projects (assay development, clinical testing, biorepository/sample management, logistics, kitting). Role is client-facing, responsible for project planning/execution, budgets, risk management, reporting, and mentoring junior PMs. Candidates must have a bachelor's in life sciences (or related) and prior experience as a Project Manager for Central Laboratories; travel ~10-25% is required.

Lead and manage central laboratory projects across assay development, clinical testing, biorepository/sample management, logistics and kitting. Responsible for planning, execution, risk and budget control, client communication, metrics and mentoring junior project managers. Role is remote (allowed countries listed), requires fluency in English and ~10-25% travel.

Precision for Medicine is hiring a remote Project Manager to lead new and existing central laboratory (CRO/pharma/biotech) projects across assay development, clinical testing, biorepository/sample management, logistics and kitting. Role is client-facing, requires cross-functional leadership, project planning/execution, risk and budget control, reporting, and mentoring junior PMs. Position accepts remote work from Poland, Serbia, Romania, Hungary, Slovakia or the United Kingdom; travel ~10-25%.

The Senior Operations Specialist leads evaluation and redesign of business processes, drives change management (including ADKAR), develops training and documentation, and establishes KPIs and dashboards to monitor operational performance. Role requires 5+ years' experience in process improvement/change management within CRO, pharmaceutical, or biotech drug development and strong English communication skills.

Responsible for providing program-level leadership and operational oversight for FSP projects, serving as primary client operational contact, coordinating cross-functional activities, monitoring risks and quality, supporting financial oversight, and contributing to onboarding and mentoring. Requires a bachelor's degree (or equivalent), strong knowledge of ICH-GCP and clinical operations, experience with clinical systems (EDC, eTMF, CTMS), and a minimum of 3 years clinical research experience with at least 2 years leading a project.

Support study teams by maintaining project timelines (MS Project), managing CTMS tasks (milestones, contacts, enrolment projections), scheduling meetings and preparing minutes, coordinating training and access, establishing SharePoint sites and project mailboxes, preparing and shipping study binders, supporting SUSAR/IND report distribution, and maintaining study trackers. Requires a 4-year degree or equivalent, minimum 2 years relevant experience, proficiency with Microsoft Office, and working knowledge of ICH-GCP.

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.

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.

The role manages the clinical data management process from study start-up through post database lock, including CRF specification, database build and UAT, edit checks, medical coding, AE/SAE reconciliation, vendor liaison, and training. Candidates should have 5+ years (Clinical Data Manager II) or 8+ years (Senior CDM) relevant experience; oncology experience and database migration experience are preferred. Position is remote with candidates considered in the UK, Poland, Hungary, Romania, Serbia, or Slovakia and may require occasional travel.

Remote role supporting clinical data management across assigned studies from start-up to post-database lock, including CRF/spec development, database build and UAT, edit checks, query and data entry oversight, medical coding and SAE/AE reconciliation. Candidates may be based in the UK, Poland, Hungary, Romania, Serbia or Slovakia. Requires professional English and 5+ years (Clinical Data Manager II) or 8+ years (Senior CDM) relevant experience; occasional travel may be required.

The Clinical Data Manager II/Senior Clinical Data Manager will manage all aspects of clinical trial data management for assigned projects, including CRF specification, database build and UAT, edit checks, medical coding, SAE/AE reconciliation, vendor coordination, documentation for the TMF, and training. Requires 5+ years as a Clinical Data Manager II or 8+ years as a Senior Clinical Data Manager; occasional travel may be required. Oncology experience and SAS familiarity are preferred.

Parexel is recruiting an experienced Clinical Project Leader / Senior Project Leader to manage global biotech clinical trials from planning through delivery. The role requires CRO clinical trial project leadership experience (Phase I–III), strong financial and client-management skills, therapeutic area expertise (oncology required; dermatology, women's health, neurology, rare disease or radiopharmaceuticals desirable) and proficiency with ICH/GCP and standard eClinical systems. Remote opportunities are available in specified EMEA countries.

Lead a multi-phased global implementation program for Veeva Quality Cloud, act as primary customer liaison, oversee release management and IT operations, and mentor project teams. Requires 8+ years' experience in IT project/program management or consulting, familiarity with SaaS and GxP, and willingness to travel 25–50%.

Responsible for conducting feasibility analyses (pre-award and post-award), site and country analysis, recruitment and epidemiology analysis, protocol review, and site outreach. Requires a bachelor’s in life sciences, minimum 5 years' related experience, professional-level English, knowledge of ICH-GCP, and proficiency with MS Office and web/data platforms. Role supports business development and study delivery across oncology and rare disease projects.

Join the Feasibility Department to deliver pre-award and post-award feasibility projects, site identification and enrollment modelling. Responsibilities include feasibility analyses (competitive, epidemiology, recruitment), protocol review, site outreach, presenting findings to BD/clients, and engaging with stakeholders including patient advocacy groups. Requires a Bachelor's in life sciences (or equivalent), minimum 5 years relevant experience, professional-level English; postgraduate degree preferred.

The Senior Feasibility Associate/Feasibility Manager will deliver pre- and post-award feasibility analyses (including recruitment, epidemiology, protocol and site/country assessments), undertake site outreach and identification, support enrollment modelling and collaborate with BD, clients, sites and partners. Requires a life sciences bachelor’s degree, minimum 5 years' relevant experience, professional English, strong data/IT and presentation skills, and knowledge of ICH-GCP. Role may be performed remotely in the listed European countries.