PpAt Johnson Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at. /p h3bJob Function /b /h3 pRD Operations /p h3bJob Sub Function /b /h3 pClinical Trial Project Management /p h3bJob Category /b /h3 pProfessional /p h3bAll Job Posting Locations /b /h3 pBeerse, Antwerp, Belgium; Breda, Netherlands; Duelmen, Germany; Imperia, Italy; Issy-les-Moulineaux, France; Leiden, Netherlands; Madrid, Spain; Warsaw, Masovian, Poland. /p h3bCompany Overview /b /h3 pOur expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science‑based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at. /p h3bPosition Summary /b /h3 pThe Lead, Trial Delivery Management (TDM) is responsible for the execution of study‑level activities, creating and updating trial‑specific documents, vendor oversight delivery, compound training, and other activities. The TDM is responsible for country and regional oversight of local operational delivery, including the alignment of the feasibility strategy and target setting, risk reviews and local challenges that could impact overall study delivery. /p h3bPrincipal Responsibilities /b /h3 ul liCreate and update critical trial‑specific documents (e.g., Monitoring Guidelines, Informed Consent Form, Investigational Medicinal Product (IMP) related documentation). /li liManage vendor set up and management of day‑to‑day study vendor activities, including set‑up, SOW creation and budget oversight. /li liResponsible for country / regional coordination of trial management activities and oversight (e.g., aligns feasibility strategy with local teams, perform country‑level risk reviews, aware of all projects conducted across countries). /li liSupport development of program‑level compound training, collaborating with Clinical / CTLD / Medical writing. /li liProvide input into trial level operational strategies. /li liResolve trial‑related issues and mitigate trial‑related risks. /li liParticipate in process improvement activities at a trial, compound cross‑DU level, as needed. /li liProvide support during Health Authority inspections and on the identification of risks and mitigation plans at the program level for key issues. /li liMentor support onboarding of new team members, particularly those in Trial Management. /li /ul h3bEducation And Experience Requirements /b /h3 h3bRequired Minimum Education /b /h3 pBS degree or equivalent, preferred areas of study include Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy). /p h3bRequired Years Of Related Experience /b /h3 pMinimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industries. /p h3bRequired Knowledge And Experience /b /h3 ul liClinical research operational knowledge and experience across multiple phases of studies (Phase I‑IV); must have the ability to manage multiple aspects of execution of a clinical trial. /li li2‑3 years’ experience supporting multiple aspects of a global clinical trial. /li liMust possess excellent leadership skills and proven ability to foster team productivity and cohesiveness. /li liExperience leading without authority and in multi‑functional matrixed and global environments. /li liExcellent decision‑making, analytical and strong financial management skills are essential to this position. /li liOperate and execute with limited supervision. Experience mentoring/coaching others. /li liStrong project planning/management, communication and presentation skills are required. /li /ul h3bOther /b /h3 h3bPercentage Travelled /b /h3 pTravel up to 15‑20% of the time, defined by business needs. /p h3bBenefits /b /h3 pWe offer a competitive salary and extensive benefits package. The health and well‑being of our employees is a priority, we have a flexible working environment as we value work‑life balance. We offer career development opportunities for those who want to grow and be part of our organization. /p h3bOffice Location /b /h3 pWe are pleased to announce that from mid‑2026, our offices in Wokingham and High Wycombe will move into a modern, state‑of‑the‑art Johnson Johnson office in central Maidenhead, conveniently situated next to the train station. /p h3bRequired Skills /b /h3 pClinical Trial Oversight, Trial Management, Vendor Management. /p h3bPreferred Skills /b /h3 pAnalytical Reasoning, Clinical Research and Regulations, Clinical Trial Designs, Clinical Trial Management Systems (CTMS), Clinical Trials, Communication, Data Savvy, Laboratory Operations, Organizing, Problem Solving, Productivity Planning, Professional Ethics, Project Integration Management, Quality Assurance (QA), Regulatory Compliance, Research and Development, Research Ethics, Standard Operating Procedure (SOP). /p pJohnson Johnson Family of Companies are equal opportunity employers, and all qualified applicants will be considered for employment without regard to any other characteristic protected by law. We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. /p /p #J-18808-Ljbffr