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Job Function:
R&D OperationsJob Sub Function:
Clinical Trial Project ManagementJob Category:
ProfessionalAll Job Posting Locations:
High Wycombe Buckinghamshire United KingdomJob Description:
Johnson & Johnson is currently seeking anOperations Specialist Patient & Site Engagementto join our Global Development Oncology Delivery Unitlocated in High Wycombe UK.
The Patient & Site Engagement (PSE) Operations Specialist serves as the primary contact for trial teams responsible for managing executing and delivering patient and site-facing initiatives in support of clinical trials. This role involves interfacing with key stakeholders within the Global Development Organization (GD) including Program Delivery Leaders (PDL) Trial Delivery Leaders (TDL) Clinical Trial Managers (CTM) Local Trial Managers (LTM) and Site Managers (SM) as well as external suppliers and other relevant stakeholders.
Services/Deliverables:
Maintain visibility of Oncology pipeline to ensure appropriate patient recruitment & retention support of relevant programs and studies
Provide patient and site insights to relevant teams to encourage thoughtful research design and execution
Ensure that executed strategies meet compliance guidelines and are delivered on time and within budget.
Work with the PSE Manager as appropriate to ensure program- and trial-level PSE deliverables are completed on schedule.
Maintain a comprehensive library of tools and tactics in the virtual Trial Master File (vTMF) ensuring effective documentation of business processes and quality standards for tactic development.
Document updates to the program- and trial-level PSE strategy including the study overview deck.
Adhere to Johnson & Johnson SOPs WIs policies local regulatory requirements and maintain compliance with relevant time reporting systems and training requirements.
Accurately oversee the Scope of Work (SOW) for External Service Providers managing PSE trial budgets and Purchase Orders proactively.
Keep the project plan updated regarding timelines and budgets aligned with the SOW for the delivery of tools and tactics for clinical trials.
Drive the execution of tactics and initiatives through the management of service providers including creative content development global translations material production and the technical development of apps and websites to enhance patient/caregiver and site engagement.
Support the PSE Manager in vendor activities such as budget tracking filing training eMP requests and issue logging.
Document compliance reviews and approvals of tools and tactics maintaining oversight for Institutional Review Board (IRB)/Ethics Committee (EC) approvals as needed.
Facilitate clear communication with all stakeholders to ensure defined expectations contributing to study meetings through facilitation attendance or presentation.
Maintain a deep understanding and proficiency in finance and contracting systems relevant to the role.
Ensure the delivery of presentations and workshop content at International Investigator Meetings Ad Hoc face-to-face meetings and similar engagements.
Metrics/KPIs:
Metrics/KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.
Interfaces:
Primary Interfaces: Trial Delivery Leader Study Responsible Physician/Scientist (SRP/S) Clinical Trial Manager (CTM)/Global Trial Manager (GTM) Local Trial Manager (LTM) Site Manager (SM) Janssen Research Procurement (JRP) Compliance Business Partners (HCC RAP Legal Privacy).
Other Interfaces: External Service Providers Investigators and Site Personnel.
Education and Experience Requirements:
Education: BA/BS or equivalent preferably in a scientific or health-related discipline.
Experience: Minimum of 3 years of relevant experience in global patient recruitment clinical trial execution or clinical research with a pharmaceutical company CRO or healthcare facility/research site.
Required Knowledge Skills and Abilities:
Experience with drug development clinical trial operations and strategic planning.
Experience in clinical trial operations including developing patient recruitment strategies ensuring patient recruitment material compliance and support programs.
Strong planning tracking customer focus organization and detail-oriented skills capable of managing multiple projects successfully.
Excellent time management prioritization and self-management skills with strong project management capabilities.
A strong team orientation demonstrating initiative to solve problems and improve efficiency and customer service.
High proficiency in Microsoft Excel PowerPoint Word and Microsoft Project.
Strong written and oral communication skills with a good understanding of relevant software and company systems.
Willingness to travel as needed.
Required Skills:
Preferred Skills:
Analytical 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)Required Experience:
IC
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