Johnson & Johnson Careers

Senior Local Trial Manager (1 of 14) - Janssen Therapeutic Areas

Raritan, New Jersey
Clinical Trial Administration

Job Description

Requisition ID: 7290171217

Janssen Research & Development, LLC, a member of Johnson & Johnson's Family of Companies, is recruiting for  Senior Local Trial Managers.  This position can be located remotely within the United States.


At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. 


Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. Please visit for more information.


The Senior Local Trial Manager (Senior LTM) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The Senior 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 Senior 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 Senior LTM may have some site management responsibilities. The Senior 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) and RTAE 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 analyze 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. Forecasts and manages country/local trial budget to ensure accurate finance reporting and trial delivered –within budget. Adheres to finance reporting deliverables and timelines.

•           Attends/participates in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting

•           Conducts local trial team meetings and provides or facilitates SM training when needed (i.e. implementation of study amendment-and changes in study related processes).

•           Reviews and approves Monitoring Visit Reports submitted by SM; identifies issues and/or trends across a trial project and escalates deviation issues to the CTM/GTL and FM as needed

•           Reviews and approves site and local vendor invoices as required. Manages local study supply, as required.

•           Prepares country specific informed consent in accordance with procedural document/templates. Reviews and manages site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations.

•           Organizes and ensures IEC/HA approvals, if applicable, and ensure that the trial is in compliance with local regulatory requirements

•           Works with SM to ensure CAPA is implemented for audits and inspection or any quality related visits

•           Complies with relevant training requirements.

•           Acts as subject matter expert for assigned protocols. Develops strong therapeutic knowledge to support roles and responsibilities. May represent GCO on cross functional teams.

•           Acts as primary local/country contact for a trial. Establishes and maintains excellent working relationships with external stakeholders, in particular investigators, study trial coordinators and other site staff; and internal stakeholders, including Medical Affairs and Marketing for Medical Affairs trials.

•           Actively contributes to process improvement, training and mentoring of CTAs, SM and other LTMs.

•           Conducts accompanied site visits with SM as delegated by FM.

•           May assumes additional responsibilities or special initiatives such as “Champion” or “Subject Matter Expert”.

•           May represents functional area in process initiatives as required

This is not an exhaustive, comprehensive listing of job functions. May perform other duties as assigned.


•           A minimum of an Associate’s degree or completion of a Nursing Program (RN) is required.  A Bachelor’s degree in a Health or Science discipline is preferred.

•           Minimum of 2 or more years of pharmaceutical and/or clinical trial experience is required.

•           Previous clinical operations experience is preferred.

•           Prior experience with any of the following Therapeutic Areas is preferred: Oncology, Neuroscience, Immunology, Cardiovascular, Metabolics, Infectious Diseases, Vaccines.

•           Solid understanding of the drug development process including GCP and local regulatory requirements is required

•           Ability to work on multiple trials in parallel preferred.

•           Some experience in mentoring/coaching and providing training to others preferred.

•           Ability to lead initiative/small teams preferred.

•           Solid leadership skills required.
•           Solid computer skills required.

•           Proficient in speaking and writing the country language and English language required.

•           Excellent written and oral communication skills required.

•           Flexible mindset and ability to work in a fast-changing environment required.

•           Minimal business travel (meetings, training, etc.) required.


Primary Location
United States-New Jersey-Raritan
Janssen Research & Development, LLC. (6084)
Job Function
Clinical Trial Administration
Requisition ID