Clinical Trial Manager

Precision for Medicine is looking for an experienced Clinical Trial Manager to join our growing team. Candidates can work remotely in the UK, Hungary, Poland, Romania, Serbia, or Slovakia. Precision for Medicine Group is a precision medicine CRO. Our integrated offering combines novel clinical trial designs, industry‑leading operational and medical expertise, advanced biomarker and data analytics solutions, and a passion for rare diseases and oncology, extending across other therapeutic areas. You will be the hub of central intelligence for the studies you manage and will lead Clinical Research Associates (CRAs) while overseeing all clinical aspects of your study across multiple countries, ensuring timeline adherence, scope, and quality delivery. We encourage high‑energy, dedicated professionals who thrive on challenge, detail, and dynamic environments. We address the challenges of oncology R&D, dedicated to positively impacting patient health worldwide. If you take a consultative approach to trial management, proving a valuable partner in operational delivery, you will play a vital role in our trials. About You Love having responsibility and a say in how clinical trials are run Plan ahead, yet remain flexible and adaptable Client‑focused with strong organizational skills to manage timelines and shifting priorities without compromising quality Communicate clearly, often, and concisely, ensuring smooth trial operation Master at identifying risks that threaten projects and resolving them resolutely Work autonomously with ownership to deliver successful outcomes Day‑to‑Day Role Manage and operationally deliver the clinical elements within a trial, including site selection, start‑up, enrolment management, site engagement, monitoring planning and execution, data cleaning, and close‑out Execute assigned trials successfully and ensure completion of trial deliverables Maintain appropriate communication, regulatory documentation, and oversight of assigned trials, collaborating closely with other functional team members Mentor and train team members Identify challenges to study timelines/deliverables and propose creative action plans to the team or sponsor Lead CRAs in establishing high‑quality site relationships for monitoring, regulatory, IP, site payment, and correspondence activities Maintain team focus on study priorities through efficient cross‑functional partnerships and effective communication to achieve the highest level of client satisfaction Qualifications Bachelor’s degree or equivalent combination of education/experience in a science or health‑related field, including oncology experience Demonstrable experience leading clinical aspects of studies across multiple countries in a CRO, pharma, or biotech company (clinical lead role) Significant oncology clinical trial management experience Working knowledge of GCP/ICH guidelines and the clinical development process Availability for domestic and international travel, including overnight stays English language proficiency Skills Computer skills (MS Office, MS Project, PowerPoint) and experience with CTMS, eTMF, EDC, IXRS Ability to develop positive working relationships with internal and external organizations Core understanding of medical terminology and clinical trial activities related to the execution of a clinical development plan Mastery of ICH‑GCP, Precision SOPs, and regulatory guidance, and the ability to implement them Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or other characteristics protected by law. #J-18808-Ljbffr Precision Medicine Group