Manager overseeing clinical site payments in hybrid work setting at Johnson & Johnson. Involved in payment processes, analytics, and team leadership for clinical trial activities.
Responsibilities
Oversee end-to-end payment process, ensuring accuracy, compliance with company policies and regulatory requirements, and adherence to contractual timelines
Work as part of a global team, collaborating with other regional managers and global leads to ensure consistency, share best practices, and optimize global payment processes
Monitor and analyze payment metrics, identifying opportunities for process improvements and efficiencies
Develop and implement training programs and SOPs for the payments team
Collaborate with cross-functional teams including colleagues within CCS including Site Contract Managers (SCMs) and study teams including Site Managers (SMs), Local Trial Managers (LTMs), and Trial Delivery Leaders (TDLs)
Assist with complex issue resolution and/or provide guidance related to site payments
Manage escalations and coordinate with internal and external stakeholders to resolve payment discrepancies or delays, ensuring timely and effective resolution
Review and consult on Clinical Trial Agreement (CTA) negotiations, specifically providing input on payment term language exceptions to ensure clarity, compliance, and risk mitigation
Proficiency in payment processing systems, clinical trial data systems, and financial software (e.g., CTMS, EDC, Ariba/SAP, etc.)
Manage work allocation and workload distribution for assigned country or regional payments team, ensuring efficient operation and coverage of all tasks
Provide people leadership through coaching, mentoring, and developing team members to build high-performing, motivated team
Foster a positive team environment, encouraging collaboration, open communication, and continuous improvement
Attract, retain, and develop talented team members by identifying growth opportunities, supporting professional development, and promoting strong team culture
Requirements
Bachelor’s degree
7-10 years’ experience and/or equivalent competencies in pharmaceutical industry/clinical research
4 years’ experience in clinical trial management or site payments within the pharmaceutical or healthcare industry
Ability to work effectively in cross-functional teams
Strong and proven analytical and problem resolution skills
Ability to demonstrate innovative spirit, have strong interpersonal skills, and ability to accomplish substantial tasks with minimal supervision
Able to reason both abstractly/conceptually as well as practically
Able to operate both at the local level and globally and connect easily at various levels in the organization
Possess strong team building skills, including collaboration, communication, knowledge sharing in a virtual and global environment
Working knowledge of PCs (MS Office suite at a minimum), SharePoint, intermediate presentation skills
Excellent communication skills (both oral and written)
Follows standard policies and procedures for multiple departments, geographic areas, client groups or projects
Fluency in English
Benefits
medical
dental
vision
life insurance
short- and long-term disability
business accident insurance
group legal insurance
consolidated retirement plan (pension)
savings plan (401(k))
vacation - up to 120 hours per calendar year
sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington - up to 56 hours per calendar year
holiday pay, including Floating Holidays - up to 13 days per calendar year
work, personal and family time - up to 40 hours per calendar year
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