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Johnson & Johnson

Associate Site Manager – Cross Therapeutic Area

Johnson & Johnson

Associate Site Manager overseeing clinical trial sites within the Innovative Medicine sector. Managing compliance, site readiness, and collaborative efforts with trial teams within a professional setting.

Posted 5/22/2026full-timeRemote • California, New Jersey • 🇺🇸 United StatesJuniorMid-Level💰 $76,000 - $121,900 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Serve as the primary contact point between the Sponsor and the Investigational Site.
  • 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.
  • Assist with site selection, site qualification assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities.
  • Partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and TDL (Trial Delivery Leader) for overall site management while performing trial related activities.
  • Execute activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management and site/study close-out according to SOPs, Work Instructions (WIs) and policies.
  • Implementation of analytical risk-based monitoring model at the site level and work with the site to ensure timely resolution of issues found during monitoring visits.
  • Ensure site staff are trained, and the corresponding training records are complete and accurate at any point during all trial phases.
  • Collaborate closely with LTM and central study team for the activities during site activation phase.
  • Ensure site study supplies are adequate for trial conduct.
  • Ensure that clinical drug supplies are appropriately used, handled and stored and returns are accurately inventoried and documented.
  • Maintain complete, accurate and timely data and essential documents in relevant systems utilized for trial management.

Requirements

What you’ll need
  • A minimum of a bachelor’s degree in pharmacy, Nursing, Life Sciences, or related scientific Discipline is required.
  • A minimum of 1 year of clinical trial monitoring experience is required.
  • Experience with Phase II and Phase III Clinical Trials is preferred.
  • Basic working knowledge of GCPs, company SOPs, local laws and regulations, assigned protocols and associated protocol specific procedures, including monitoring guidelines, is required.
  • Strong computer skills in appropriate software applications and related clinical systems required.
  • Must have strong written and oral communication skills.
  • Willingness to travel up to 60% with overnight stay away from home is required.
  • A valid Driver's License issued in one of the 50 United States and a good driving record is required.

Benefits

Comp & perks
  • medical
  • dental
  • vision
  • life insurance
  • short- and long-term disability
  • business accident insurance
  • group legal insurance
  • consolidated retirement plan (pension)
  • savings plan (401(k))
  • long-term incentive program
  • vacation - 120 hours per calendar year
  • sick time - 40 hours per calendar year; for employees who reside in the State of Washington - 56 hours per calendar year
  • holiday pay, including Floating Holidays - 13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • Parental Leave - 480 hours within one year of the birth/adoption/foster care of a child
  • Condolence Leave - 30 days for an immediate family member: 5 days for an extended family member
  • Caregiver Leave - 10 days
  • Volunteer Leave - 4 days
  • Military Spouse Time-Off - 80 hours

ATS Keywords

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Hard Skills & Tools
clinical trial monitoringGCPSOPsite managementrisk-based monitoringdata managementsubject recruitmentsite qualification assessmentsite initiationsite close-out
Soft Skills
communication skillscollaborationorganizational skillsproblem-solvingattention to detailtrainingtime managementinterpersonal skillsadaptabilityteamwork
Certifications
Bachelor's degree in pharmacyBachelor's degree in NursingBachelor's degree in Life SciencesClinical Research Certification (preferred)