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  1. Home
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  5. Associate Site Manager - Cross Therapeutic Area - California
Johnson & Johnson logo

Associate Site Manager - Cross Therapeutic Area - California

Not Disclosed•Full-TimeRemote

location_onMichael's Inn, 46, Thompson Street, Raritan, Somerset County, New Jersey, 08869, United States

Apply Now

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 the Team

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

We are searching for the best talent for an Associate Site Manager – Cross Therapeutic Area. This is a remote role available within the state of California. 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.

In this role, you will partner with the Local Trial Manager, Clinical Trial Assistant, and Trial Delivery Leader to ensure overall site management. You will assist with site selection, qualification assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring, and close-out activities. You will contribute to process improvement and training while receiving guidance from a Senior Site Manager.

Hiring Process

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 jnj.com. Internal employees should 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.

Work location

Work model: Remote

location_on

Michael's Inn, 46, Thompson Street, Raritan, Somerset County, New Jersey, 08869, United States

Raritan, New Jersey

Key Responsibilities

  • check_circleAct as primary local contact between sponsor and investigational sites for assigned trials
  • check_circleEnsure site staff training records are complete and accurate throughout all trial phases
  • check_circleCollaborate with team to complete Corrective Action Preventative Action (CAPA) for audits
  • check_circleParticipate in Health Authority and Ethics Committee submission and notification processes
  • check_circleReport Adverse Events (AEs) and Serious Adverse Events (SAEs) within required timelines
  • check_circleParticipate in site feasibility assessments and Site Qualification Visits (SQVs)
  • check_circleEnsure data accuracy, validity, and timely resolution of data entry queries
  • check_circleDocument trial activities, write visit reports, and maintain essential study documents
  • check_circleExecute site initiation, monitoring, management, and close-out activities per SOPs and GCP

Requirements

  • verifiedBachelor's degree in pharmacy, Nursing, Life Sciences, or related scientific Discipline
  • verifiedMinimum of 1 year of clinical trial monitoring experience
  • verifiedBasic working knowledge of GCPs, company SOPs, local laws and regulations
  • verifiedStrong computer skills in appropriate software applications and related clinical systems
  • verifiedStrong written and oral communication skills
  • verifiedValid Driver's License issued in one of the 50 United States and a good driving record

Nice to Have

Experience with Phase II and Phase III Clinical Trials.

Benefits & Perks

check_circleMedical, dental, vision, life, short- and long-term disability, business accident, and group legal insurancecheck_circleConsolidated retirement plan (pension) and 401(k) savings plancheck_circleLong-term incentive programcheck_circle120 hours of vacation per calendar year40 hours of sick time per calendar year
Johnson & Johnson logo
Company

Johnson & Johnson

Industry

healthcare & nursing

View company profilearrow_forwardlanguageWebsite
Quick Overview

Experience

1+ yrs (Entry Level)

Education

Minimum of a bachelor's degree in pharmacy, Nursing, Life Sciences, or related scientific Discipline is required.

Job Type

Full-Time

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Skills, education and keywords

Skills: GCP, Sop, Clinical Trials, Clinical Trial Monitoring, Phase Ii Clinical Trials, Phase Iii Clinical Trials, Clinical Data Management, Clinical Trials Operations, Laboratory Operations, Process Improvements.

Education: Minimum of a bachelor's degree in pharmacy, Nursing, Life Sciences, or related scientific Discipline is required..

Frequently asked questions about Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson

What does a Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson do?expand_more
Day-to-day, the Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson will act as primary local contact between sponsor and investigational sites for assigned trials; ensure site staff training records are complete and accurate throughout all trial phases; collaborate with team to complete corrective action preventative action (capa) for audits; and participate in health authority and ethics committee submission and notification processes.
What are the requirements for this Associate Site Manager - Cross Therapeutic Area - California 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; Minimum of 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; Strong written and oral communication skills; and Valid Driver's License issued in one of the 50 United States and a good driving record.
Where is the Associate Site Manager - Cross Therapeutic Area - California role at Johnson & Johnson located?expand_more
Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson is based in Michael's Inn, 46, Thompson Street, Raritan, Somerset County, New Jersey, 08869, United States. This is a remote role.
Is this Associate Site Manager - Cross Therapeutic Area - California job remote, hybrid, or on-site?expand_more
Johnson & Johnson has listed this Associate Site Manager - Cross Therapeutic Area - California role as remote.
How much experience is required for this Associate Site Manager - Cross Therapeutic Area - California role?expand_more
Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson typically requires 1+ years of relevant experience at the entry level level.
What skills do you need for the Associate Site Manager - Cross Therapeutic Area - California role at Johnson & Johnson?expand_more
Key skills for Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson include GCP; Sop; Clinical Trials; Clinical Trial Monitoring; Phase Ii Clinical Trials; Phase Iii Clinical Trials; Clinical Data Management; and Clinical Trials Operations.
What education is required for Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson?expand_more
Educational requirements for this role: Minimum of a bachelor's degree in pharmacy, Nursing, Life Sciences, or related scientific Discipline is required..
What category does the Associate Site Manager - Cross Therapeutic Area - California role belong to?expand_more
Associate Site Manager - Cross Therapeutic Area - California at Johnson & Johnson is part of the healthcare & nursing job category on Recrutus.
Recrutus

Curating the world's most innovative career opportunities. We bridge the gap between visionary talent and industry-leading companies.

Search roles by city, category, skill, or job type — explore verified US employers, salary benchmarks, and remote-friendly teams hiring nationwide.

publiclanguageshare
Job seekers
Browse jobsCompanies hiringRemote jobsJobs by locationJobs by cityJobs by categoryJobs by skillCareer guidesCareer blogSalary insights
Job types
Contractor jobsFull-Time jobsIntern jobsOther jobsPart-Time jobsPer-Diem jobsTemporary jobs
Top states
Jobs in TexasJobs in New YorkJobs in CaliforniaJobs in ArizonaJobs in MassachusettsJobs in FloridaAll states →
Top categories
Healthcare & Nursing jobsLogistics & Warehouse jobsEngineering jobsIT jobsHospitality & Catering jobsTravel jobsSales jobs
Popular skills
CDL A jobsRegistered Nurse jobsBLS jobsAcls jobs
Featured employers
Company
About usFAQContactPrivacy policyUS privacy notice

Recrutus helps candidates discover roles that match their skills and helps teams reach qualified applicants faster. Browse by metro, discipline, or work style — from internships to senior leadership.

© 2026 Recrutus. All rights reserved.
Terms of serviceCookie policyAcceptable useDMCA policyEmployer termsCandidate terms
  • check_circleContribute to site-level recruitment strategies and contingency planning
  • check_circleTrack site-level costs and ensure timely payments are processed
  • check_circleManage clinical drug supplies including storage, usage, inventory, and destruction
  • check_circle
    check_circle13 days of holiday pay including floating holidays
    check_circleUp to 40 hours of work, personal, and family time per calendar year
    check_circle480 hours of parental leave within one year of birth, adoption, or foster care
    check_circle30 days of condolence leave for immediate family members
    check_circle10 days of caregiver leave and 4 days of volunteer leave

    Skills Required

    GCPSopClinical TrialsClinical Trial MonitoringPhase Ii Clinical TrialsPhase Iii Clinical TrialsClinical Data ManagementClinical Trials OperationsLaboratory OperationsProcess Improvements
    Accessibility