Lead Clinical Data Analyst

At 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 jnj.comAs 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.Job Function: Data Analytics & Computational SciencesJob Sub Function: Clinical Data ManagementJob Category:ProfessionalAll Job Posting Locations:Leeds, West Yorkshire, United Kingdom, Raynham, Massachusetts, United States of America, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of AmericaJob Description:We are searching for the best talent for a Lead Clinical Data Analyst to join our DePuy Synthes team located in Warsaw, IN; Raynham, MA; West Chester, PA; Leeds, West Yorkshire (UK)Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.Are you passionate about improving and expanding the possibilities of Orthopedics? Ready to join a team that’s reimagining how we heal? Our Orthopedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery.Your unique talents will help patients on their journey to wellness. Learn more at Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.Purpose: The Lead Clinical Data Analyst will coordinate timelines and resources required to implement and maintain a variety of clinical systems as well as provide oversight and coordination of all aspects of the development and management of clinical study databases across a variety of platforms. Coordination of activities will require the development of strong, productive relationships with colleagues across the MD sector. You will:Collaborate with Data Management leadership (including Programming and Biostatistics) to define and document data and process standardsProvide in-house project support for creation, routing and approval of all system deliverables associated with clinical systemsSupport the development and maintenance of global harmonized processes and procedures for system supportSupport vendor evaluation, selection, contracting, and oversight activities for outsourced systems; Assist with vendor evaluation and selection activities for clinical systemsWork with BSDM partners, and leadership in Clinical Operations and Franchise to develop project management plans for trial execution including timelines and milestones for study-specific systems set-up, UAT, maintenance and closeout as requiredLead project management activity related to the deployment of Interactive Voice/Web Response Systems (IxRS), Electronic Data Capture (EDC) Systems, CTMS, eTMF and other relevant platforms (as assigned)Create, review and facilitate approval of system deliverables and facilitate appropriate quality review where applicableMentor peers through review of deliverables to minimize delays during the quality review processInterface between Clinical R&D, IT and Quality including CSV regarding clinical systems, UAT, processes and other toolsFacilitate support requests associated with clinical systems (as needed)Serve as first line of contact from study initiation through go live for each clinical study. Systems may include: CTMS, eTMF, IxRS, EDCsFacilitate the development of training materials and programs related to system set-up, UAT and ongoing maintenance as well as other relevant processesRepresent the Medical Devices Sector on Enterprise or cross-sector Clinical System teams (as needed)Assist with the implementation of study metricsAnalyzes complex change requests to determine feasibility for incorporation within clinical studiesEvaluates vendor supplied release documentation for implementation feasibility and collaborate with appropriate partners to define project parametersResponsible for communicating business related issues or opportunities to next management levelResponsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and proceduresPerforms other duties assigned as neededQualifications: A Bachelor’s degree (or equivalent) in Statistics, Computer Science or related discipline (required), with at least 6 years of system support in clinical research within Medical Device or PharmaceuticalsExperience with at least one clinical system (EDC, CTMS, eTMF and IxRS) is required; Strong proficiency in more than one Clinical system preferred. Advanced certification preferredDemonstrated ability to manage a project in a team environment to deliver critical milestones requiredMust have proven experience with Medidata or Veeva systems Excellent verbal and written communication skills requiredPrevious experience in Clinical Operations preferredExperience with CDISC STDM preferredKnowledge of GCP and SDLC preferredTravel up to 10%#LI-AM2Johnson & 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. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (View email address on click.appcast.io) or contact AskGS to be directed to your accommodation resourceRequired Skills:Preferred Skills:Advanced Analytics, Clinical Data Management, Clinical Operations, Collaborating, Communication, Database Management, Data Quality, Data Savvy, Good Clinical Practice (GCP), Innovation, Interdisciplinary Work, Problem Solving, Process Improvements, Research Ethics, Resource Allocation, Training PeopleThe anticipated base pay range for this position is :$109,000.00 - $174,800.00Additional Description for Pay Transparency:SummaryLocation: Warsaw, Indiana, United States of America; West Chester, Pennsylvania, United States of America; Leeds, West Yorkshire, United Kingdom; Raynham, Massachusetts, United States of AmericaType: Full time