# Sr Local Trial Manager at Johnson & Johnson

Johnson & Johnson is hiring a Sr Local Trial Manager in Beijing, China. Level rates it Little AI ●○○○; you can [apply on Level](https://jobsbylevel.com/go/c6f94377-5a0a-4850-99f4-149c27f8470e?utm_medium=ai-agent).

AI Level 1, AI centrality 0 out of 100. Beijing, China.

## Details

- Company: [Johnson & Johnson](https://jobsbylevel.com/companies/johnson-johnson)
- AI level: AI Level 1 (score 0 out of 100)
- Location: Beijing, China
- Posted: October 19, 2026
- Apply: https://jobsbylevel.com/go/c6f94377-5a0a-4850-99f4-149c27f8470e?utm_medium=ai-agent

## Prepare for this job

The job page lists 4 likely interview questions for this offer, with a CV checklist: https://jobsbylevel.com/jobs/sr-local-trial-manager-at-johnson-johnson-89a48b

## Description

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.com . As 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: R&D Operations Job Sub Function: Clinical Trial Project Management Job Category: Professional All Job Posting Locations: Beijing, China, Shanghai, China Job Description: Position Summary: The Sr Local Trial Manager (Sr LTM) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The Sr LTM is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents. The Sr LTM is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements. The LTM II actively contributes to process improvement; training and mentoring of Clinical Trial Assistants (CTA), Site Managers (SM) and other LTM roles. The Sr LTM may have some site management responsibilities. The Sr LTM may also perform the role of Clinical Trial Manager (CTM)/Global Trial Lead (GTL) for single country as described in GCO procedural documents. Principal Responsibilities: Collaborate with Functional Manager (FM)/Clinical Research Manager (CRM) for country protocol feasibility (if applicable) and site feasibility assessment in conjunction with CTA (if applicable), SM and CTM/GTL. Implements any local criteria for site selection. Ensure consistent conduct of pre-trial assessment visits and instruct teams on appropriate follow-up of pre-trial visit report and country feasibility report. Recommends suitable sites for selection to participate in trial. Collaborates with the Global Product Lead (GPL), CTM/GTL, local management/Country Head and other study team member to select final site list. Contributes input to the study management documents at a country level or initiates development of these documents for a single country trial, as per SOPs Leads and coordinates local trial team activities in compliance with SOPs, other procedural documents and applicable regulations. Leads local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget. Including but not limited to: development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting. Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs)/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate. Maintains and updates trial management systems. Uses study tools and management reports available to analyse trial progress Monitors country progress and initiates corrective and preventive actions (CAPA) when the trial deviates from plans and communicates study progress and issues to study management teams. May submit requests for vendor services and may support vendor selection. In certain situations, may assist in negotiation of trial site contracts and budgets.

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Source: https://jobsbylevel.com/jobs/sr-local-trial-manager-at-johnson-johnson-89a48b

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