Senior Specialist, Clinical Risk Management

Job Function Quality Job Sub Function Clinical Quality Job Category Professional Job Posting Locations Horsham, Pennsylvania, United States of America; Raritan, New Jersey, United States of America; Spring House, Pennsylvania, United States of America; Titusville, New Jersey, United States of America Job Description Johnson & Johnson is currently seeking a Senior Specialist, Clinical Risk Management to join our R&D Quality CRM team located at J&J offices in Horsham, PA; Spring House, PA; Titusville, NJ or Raritan, NJ. Purpose The Senior Specialist, Clinical Risk Management works with the trial teams to coordinate the identification, assessment, and mitigation of quality risks that could impact trial data integrity, patient safety, wellbeing or rights. Throughout the duration of the trial, the Senior Specialist executes data‑driven, risk‑based trial oversight activities to deliver quality in the execution of trials, compliance with regulatory requirements and internal procedures, and to maintain a continued state of inspection readiness. Key Responsibilities Actively participate in all study activities, contributing to the identification and assessment of key risks in the clinical protocol/set‑up and advising clinical team members on effective mitigation strategies. Participate in regular review of risk areas in collaboration with Risk Owners, to evaluate progress of risk mitigations and risk reduction, and to identify potential new risks or additional mitigation needs (trial and/or compound, as assigned). Maintain CQP (Clinical Quality Plans) in quality repository to facilitate regular progress reviews of quality support services in addition to risks and mitigations. Collaborate closely with risk owners in evaluation of mitigation actions and effectiveness checks on mitigations. Communicate and facilitate risk updates to R&D colleagues as part of the regular review cycle through Quality Working Groups and Governance Fora, as applicable (trial and/or compound, as assigned). Highlight new potential systemic risk to RDQ CRM management. Develop and ensure a consistent interpretation of issues that require quality investigations. Provide guidance for significant quality issues (SQI) per corporate standards and escalates SQI to senior R&D management. Provide initial serious breach evaluation of quality issue that may require reporting to Health Authorities. In collaboration with partners in RDQ, provide advice on the development and implementation of Corrective and Preventative Action (CAPA) Plans and Effectiveness Checks (Self‑Identified, Inspection, Audit). Support proactive inspection readiness activities throughout the study with trial teams to develop ongoing trial oversight, inspection narratives, identify and prepare sites of interest for inspection (including pre‑inspection visit support), ensure availability of key documents/records and coordinate mock inspection in collaboration with Regulatory Compliance teams. Provide support for investigator, sponsor‑monitor and third‑party inspections including post inspection support. Provide advice on questions related to research quality and compliance from Business Partners in collaboration with other Quality Professionals and Subject Matter Experts to ensure consistent interpretation of international regulations and policy. Qualifications Minimum of a Bachelor's degree (scientific, medical, or related discipline). Minimum of 6 years working in the healthcare industry (pharmaceutical industry, contract research organization and/or healthcare/hospital system). Excellent interpersonal, oral, and written communication skills. GCP quality and/or clinical trials experience. Experience collaborating in a cross‑functional team environment. Flexibility to respond to changing business needs. Demonstrated ability to operate in an environment of culturally diverse styles and business approaches by understanding regional and global business structures. Proficiency in Microsoft Office Applications. Experience with fundamentals of clinical trial risk management, preferably in a global setting. Experience working to ICH guidelines. Health Authority Inspection experience (FDA, EMA and other inspectorates). Strong Project Planning/Management skills. Experience and/or proficiency with data analytics and/or data visualization tools (Tableau, Spotfire, or related). Proven ability to analyze & interpret collective data to provide insights to drive decision‑making. Experience in managing escalations and CAPA support/advisement. Experience with Data Science and Digital Health (including Real World Evidence/Real World Disease). Proficiency in speaking and writing English. Up to 10% travel, primarily domestic with some international travel. Equal Opportunity Employer Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. Pay Transparency The anticipated base pay range for this position is: $94,000.00 - $151,800.00. Benefits Vacation – 120 hours per calendar year. Sick time – 40 hours per calendar year (48 hours for Colorado, 56 hours for Washington). Holiday pay, including floating holidays – 13 days per calendar year. Work, personal and family time – up to 40 hours per calendar year. Parental leave – 480 hours within one year. Bereavement leave – 240 hours for immediate family, 40 hours for extended family per calendar year. Caregiver leave – 80 hours in a 52‑week rolling period. Volunteer leave – 32 hours per calendar year. Military spouse time‑off – 80 hours per calendar year. #J-18808-Ljbffr Johnson & Johnson Innovative Medicine