Clinical Research Manager - JJMT Electrophysiology

Clinical Research Manager – JJMT Electrophysiology

Location:

Irvine, California, United States of America

Our J&J Med Tech Electrophysiology clinical team is currently recruiting for a Clinical Research Manager
. The preferred location is Irvine, CA on a hybrid work schedule of 2‑3 days a week onsite. We are open to remote applicants.

Johnson & Johnson believes 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 Med Tech, 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.

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Under limited supervision, this Clinical Research Manager will provide leadership to a team of Clinical Research Leaders (CRLs) and Clinical Research Specialists (CRSs) and ensure the successful performance and delivery of project deliverables, on time with high quality. The Clinical Research Manager will be responsible for encouraging strong, positive relationships with co‑workers across the organization.

• Serves as a Clinical Research Manager within the Clinical R&D Department to execute and manage company-sponsored clinical trials, ensuring monitoring compliance with timelines and study milestones for JNJ Med Tech – Electrophysiology.
• Provide leadership and oversight for monitoring activities of clinical trials, aligning activities with broader study objectives, and providing input on trial design to optimize monitoring efficiency and effectiveness.
• Experience documenting and sharing insights into trial monitoring activities (e.g., trends in protocol compliance, enrollment, monitoring deviations, data quality); external partners e.g. principal investigators and support staff, and internal partners e.g. study team, management and leadership staff.
• Contribute to the oversight of feasibility, selection, set-up, conduct and closure of a clinical trial as related to monitoring activities within the allocated countries, in accordance with the ICH‑GCP, applicable legislation and Company Standard Operating Procedures.
• Perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close-out visits.
• May be involved in the management and oversight of device ordering, tracking, and accountability of investigational products and trial materials.
• May be involved in the team’s interface and collaboration with key opinion leaders, site investigators, IRBs/ECs, Regulatory agencies, contractors/vendors, societies, associations and company personnel.
• Provide input on clinical data review to prepare data for statistical analyses and publications.
• Lead on-site procedural protocol compliance and data collection to the clinical trial sites.
• Responsible for delivery of monitoring deliverables for assigned clinical projects, through effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs).
• May liaise with regional partners to ensure global standard processes are shared and applied across the organization.
• Plans, tracks and manages assigned monitoring project budgets to ensure adherence to business plans.
• Ensures resources assigned to designated clinical trials to provide quality deliverables while maintaining efficiency.
• Functions as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders.
• Should develop a strong understanding of the pipeline, product portfolio and business needs.
• Manages work independently. Independently solves problems arising during clinical trial execution, and will seek guidance for more complex problems, as needed.
• Responsible for communicating business-related issues or opportunities to next management level.
• Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
• For those who…