Associate Site Manager, Clinical Trial Support
Not Disclosed•Full-TimeRemote
location_onRemote
About Johnson & Johnson
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.
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. We respect the diversity and dignity of our employees and recognize their merit.
About Innovative Medicine
Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
About the Role
Johnson & Johnson Innovative Medicine R&D is recruiting for an Associate Site Manager - Cross TA & Immunology Central U.S. This position can be located remotely in Texas to support the Central Region of the United States.
The Associate Site Manager will serve as the primary contact point between the Sponsor and the Investigational Site. You will be assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure. You will partner with the Local Trial Manager, Clinical Trial Assistant, and Trial Delivery Leader to ensure overall site management while performing trial-related activities for assigned protocols. This role offers the opportunity to contribute to process improvement and training while receiving guidance from a Senior Site Manager.
Hiring Process & Application
This job posting is anticipated to close on May 20, 2026. The Company may extend this time-period, in which case the posting will remain available on https://www.careers.jnj.com to accept additional applications.
Johnson & 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, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.
Equal Opportunity
Johnson & 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.
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Skills, education and keywords
Skills: GCP, Sop, Clinical Trial Monitoring, Phase Ii Clinical Trials, Phase Iii Clinical Trials, Clinical Data Management, Clinical Operations, Clinical Research And Regulations, Clinical Trial Designs, Clinical Trials Operations.
Education: Minimum Bachelor's degree in Pharmacy, Nursing, Life Sciences, or related scientific discipline required.
Frequently asked questions about Associate Site Manager, Clinical Trial Support at Johnson & Johnson
What does a Associate Site Manager, Clinical Trial Support at Johnson & Johnson do?expand_more
A Associate Site Manager, Clinical Trial Support at Johnson & Johnson is responsible for the following: Act as primary contact between sponsor and investigational sites for assigned clinical trials; Ensure site staff training records are complete and accurate throughout all trial phases; Report and document Adverse Events and Serious Adverse Events within required timelines; and Prepare trial sites for close-out and conduct final close-out visits.
What are the requirements for this Associate Site Manager, Clinical Trial Support role?expand_more
Johnson & Johnson is looking for candidates who meet the following requirements: Bachelor's degree in Pharmacy, Nursing, Life Sciences, or related scientific Discipline; 1 year of clinical trial monitoring experience; Basic working knowledge of GCPs, company SOPs, local laws and regulations; Strong computer skills in appropriate software applications and related clinical systems; Valid Driver's License issued in one of the 50 United States and a good driving record; and Willingness to travel up to 60% with overnight stay away from home.