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. /p pLearn more at jnj.com. /p pAs guided by Our Credo, Johnson Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson Johnson, we respect the diversity and dignity of our employees and recognize their merit. /p h3Job Function /h3 pRD Operations /p h3Job Sub Function /h3 pClinical Trial Support /p h3Job Category /h3 pProfessional /p h3All Job Posting Locations /h3 pBeerse, Antwerp, Belgium, Breda, Netherlands, Copenhagen, Istanbul, Turkey, Madrid, Spain, Milano, Italy, Neuss, North Rhine-Westphalia, Germany, Paris, Île-de-France, France, Prague, Czechia, Solna, Stockholm County, Sweden, Warsaw, Masovian, Poland /p h3Job Description /h3 pThe GCO Leadership Development Program consists of 12 months of dynamic rotations with in-depth training across the CTA, SM, LTM roles, supported by strong line management, formal mentorship, sponsorship, networking, focused leadership development and dynamic real world work experience. /p pGlobal Trial Associates (GTAs) will rapidly gain knowledge, develop technical and leadership skills and important insights into how the business operates. /p pThe objective is for the GTA to develop an understanding of pharmaceutical development, GCO standard operation procedures, policies and regulatory requirements, logistical and administrative tasks related to trial management (start-up, execution and closing phases) and patient safety in clinical trials. /p pThe GTA will gain knowledge of and support activities of the Site Manager (SM) and Local Trial Manager (LTM) positions under the direct supervision of LTM and SM mentors, Program Manager, and/or Functional Manager (FM). /p pUpon successful completion of the program, GTAs will be placed in either the LTM or SM role depending on business need and skill set of the GTAs. /p h3Responsibilities /h3 ul liProvide administrative and logistical support to Clinical Trial Assistant (CTAs), SM and/or LTM in tracking progress of the trial, management of study data, budget, organizing meetings, mailing and correspondence, materials, drug distribution and other relevant tasks as appropriate in adherence to relevant SOPs, policies, and local regulatory requirements. /li liSupport the local study team in performing site feasibility and/or country feasibility. Collaborates with the Global Project Team, e.g. Clinical Trial Manager (CTM)/Global Trial Lead (GTL), local management/Country Head and other study team members, as required. /li liMaintain information in relevant systems, including electronic filing (electronic Trial Master File: eTMF). /li liEnsure current versions of the required trial documents, trial-related materials and supplies are provided to the investigational site within required timeframes, as applicable. /li liSupport CTA, SM and/or LTM in collecting/preparing documents required for study start-up/ submission to Ethics Committee/IRB and/or Health Authorities. /li liSupport CTA SM and/or LTM in collecting, processing, and archiving study related documents as appropriate. Use appropriate systems to ensure file completeness at designated study milestones. /li liMay assist team in conducting local investigator meeting or with planning for the investigators participating in an international meeting. /li liMaintain and update contact information in relevant systems to ensure appropriate safety updates distribution. /li liComply with all training requirements, company policies procedures and all applicable laws and regulations. Always act aligned with JJ Credo. /li liEnsure inspection readiness at all times. /li liMay contribute to process improvement. /li liSupport SM and within a reasonable timeframe be able to take on responsibility in executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/ study close-out according to Standard Operating Procedures, Work Instructions (WIs) and policies. /li /ul pThis is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned. /p h3Education And Experience Requirements /h3 ul liMust be graduating no more than 12 months prior to the target start date of July 2026, with a Bachelor’s or Master’s degree (e.g., BA, BS, MS), in Health Sciences or related scientific field. /li liProven strong academic performance. /li liOne plus years of work experience preferred. /li liRequirement for IT literacy relevant to Corporate and Clinical Operations. /li liMust be authorised to work in the country of application and must not require sponsorship at the time of hire. /li liFluency in the local language of the country where the application is submitted is required. /li /ul h3Other Skills /h3 ul liStrong verbal and written communication and presentation skills. /li liAnalytical and a real problem solver. /li liWillingness to learn in a dynamic environment and stay abreast of new technologies. /li liStrong interpersonal, leadership, and negotiating skills. /li liExcellent organizational skills and the ability to collaborate and handle multiple priorities within a matrix environment. /li liAbility to perform activities in a timely and accurate manner. /li liExpert proficiency with Word, Power Point, Excel. /li /ul h3Travel /h3 pWhile in the Site Manager rotation, approximately 25% travel. /p h3Preferred Skills /h3 ul liAnalytical Reasoning /li liBusiness Behavior /li liBusiness English /li liClinical Data Management /li liClinical Trials /li liClinical Trials Operations /li liExecution Focus /li liIssue Escalation /li liLaboratory Operations /li liProcess Improvements /li liProcess Oriented /li liProject Support /li liRegulatory Environment /li liResearch and Development /li liResearch Ethics /li liStudy Management /li liTime Management /li /ul /p #J-18808-Ljbffr