Parexel is hiring a Senior Clinical Trial Associate (Project Specialist) to provide logistical and operational support to global study management teams. Responsibilities include TMF maintenance, CTMS tracking, IRB/HA submission support, clinical trial supplies coordination, vendor/CRO liaison, meeting organization and study documentation tracking. Role is home based in Poland, Spain, Serbia or Romania; requires a bachelor's degree (life sciences or nursing preferred), minimum 2 years' relevant experience and proficiency in English. Base pay range for Poland: PLN 120,000–160,000 per year.

Responsible for coordinating communication between Suvoda eCOA teams, instrument license holders, and translation vendors; researching licensing and eCOA requirements; preparing and proofreading screen reports and .json files; and managing related timelines. Requires a bachelor's degree and 2+ years' experience in the pharmaceutical industry, strong licensing experience, and project management skills.

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.

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.

The Start Up Lead will own execution of site start-up strategy and coordination across countries (UK, Hungary, Poland, Romania, Serbia, Slovakia), act as SME and trainer for site start-up activities, manage milestone planning and risk mitigations, and coordinate regulatory/contract deliverables. Requires a bachelor's in life sciences or RN (or equivalent), minimum 5 years start-up experience, and fluency in English; occasional travel may be required. Salary estimate for Poland: 209,300–313,900 PLN gross/year.

The Start Up Lead will manage and coordinate site start-up activities (IRB/EC & CA/MoH submissions, ICF customization, IMP release), develop activation readiness and critical path plans, liaise with stakeholders and clients, mentor staff, and use tracking tools to ensure timely site activation. Role may be performed remotely from UK, Hungary, Poland, Romania, Serbia or Slovakia and requires a minimum of 5 years start-up experience.

The Start Up Lead will manage and coordinate site start-up activities across multiple countries (UK, Hungary, Poland, Romania, Serbia, Slovakia), including IRB/EC and CA/MoH submissions, ICF customization, IMP release packaging, milestone planning and tracking, contract and budget negotiations, stakeholder communication, training/mentoring, and oversight of country-specific start-up processes. Requires a bachelor's in life sciences or RN and 5+ years' start-up experience in CRO or pharma/biotech.

The Start Up Lead will manage and coordinate global site start-up activities (ICF customization, IRB/EC & CA/MoH submissions, IMP release, contract and budget negotiations), act as SME and trainer for start-up processes, collaborate with cross-functional stakeholders, maintain tracking systems, and may perform occasional travel. Role can be performed remotely from the UK, Hungary, Poland, Romania, Serbia, or Slovakia.

Remote Start Up Lead responsible for execution of site start-up strategy and critical-path planning (IRB/EC & CA/MoH strategy, ICF customization, IMP release), coordinating translations, tracking milestones, managing risks, liaising with stakeholders and mentoring staff. Role requires a bachelor's degree (life sciences or RN) and minimum 5 years' start-up experience across multiple countries. Occasional travel may be required.

The Start Up Lead oversees site start-up activities including IRB/EC and CA/MoH submissions, ICF customization, IMP release packages, milestone planning and risk mitigation. Requires 5+ years start-up experience, leadership in cross-functional coordination, and fluency in English; local language proficiency is required where applicable. Role may involve occasional travel and client-facing activities.

Parexel FSP seeks an IRT Vendor Start-up Manager to provide technical IRT vendor expertise through study start-up to close-out, enabling timely site readiness and vendor service delivery. Requires 3+ years' clinical operations/IRT vendor management experience, knowledge of GxP and ICH, UAT experience, and skills in vendor selection, contract/procurement support, budget/invoice reconciliation, risk management and stakeholder collaboration.

Responsible for implementing eClinical technology for studies, including requirements gathering, design, configuration and integrations; primary contact for study technology with internal teams and external clients. Requires clinical trials experience, familiarity with CTMS/EDMS/EDC/IVRS, knowledge of CDISC SDTM, ICH-GCP and 21 CFR Part 11, and strong project/client management and communication skills.

Remote Clinical Trial Manager role in a precision medicine CRO responsible for operational delivery of clinical trial elements (site selection, start-up, enrolment, monitoring, data cleaning, close-out) across multiple countries. Requires experience leading multi-country clinical studies (oncology), working knowledge of GCP/ICH, ability to travel internationally, and effective English communication.

Manage and deliver clinical trial activities across multiple countries including site selection, start-up, enrollment management, monitoring, data cleaning and close-out. Role requires significant oncology trial management experience in a CRO/Pharma/Biotech setting, working knowledge of ICH-GCP, ability to mentor CRAs, and availability for domestic and international travel.

Precision for Medicine seeks a Clinical Trial Manager (remote) to manage and operationally deliver clinical elements of oncology trials across multiple countries (UK, Hungary, Poland, Romania, Serbia, Slovakia). Responsibilities include site selection and start-up, enrolment management, monitoring, data cleaning, close-out, leading CRAs, regulatory documentation, and cross-functional communication. Requires demonstrable multi-country clinical lead experience in a CRO/Pharma/Biotech setting, strong knowledge of ICH-GCP, and effective English communication. Availability for domestic and international travel is required.

Experienced Clinical Trial Manager role (remote) within a precision medicine CRO focused on oncology and rare diseases. Candidate will manage clinical elements across multi-country trials including site selection, start-up, enrolment management, monitoring, data cleaning and close-out; lead and mentor CRAs; ensure communication, regulatory oversight and adherence to ICH-GCP and company SOPs. Bachelor’s degree in a science or health-related field is required; significant clinical trial management experience in oncology and availability for domestic/international travel are expected. Required familiarity with CTMS, eTMF, EDC, IXRS and MS Office tools.

Precision for Medicine seeks an experienced Clinical Trial Manager to lead clinical aspects of multi-country oncology and rare-disease trials. Responsibilities include site selection, start-up, enrollment management, monitoring oversight, data cleaning, close-out, leading CRAs, and ensuring regulatory documentation and timeline adherence. Role requires demonstrable clinical trial management experience in CRO/Pharma, working knowledge of ICH-GCP, and availability for domestic and international travel.

Remote Clinical Trial Manager role in a precision medicine CRO responsible for site selection, start-up, enrollment management, monitoring planning/execution, data cleaning, regulatory documentation, and close-out across multiple countries (UK, Hungary, Poland, Romania, Serbia, Slovakia). Requires significant clinical trial management experience (oncology), working knowledge of ICH-GCP, and effective English communication. Role includes mentoring CRAs and cross-functional collaboration; domestic and international travel required.

Responsible for implementing eClinical platforms for studies, gathering and documenting requirements, configuring systems (CTMS, EDMS, EDC, IVRS), coordinating global virtual teams, managing client communications, ensuring compliance with SOPs/ICH-GCP/21 CFR Part 11, and supporting timely, high-quality delivery. Role can be fully home based in Romania, Serbia, Poland, or South Africa.

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.