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Director, Site Management – Monitoring
PfizerDirector of Site Management overseeing resources for clinical trial activities in the U.S. Collaborating cross-functionally to ensure quality execution of clinical trials at investigational sites.
Posted 7/23/2026full-timeRemote • New York • 🇺🇸 United StatesLead💰 $176,600 - $294,300 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive clinical research experience and knowledge of clinical trial methodologies, with a strong ability to lead and manage diverse teams while ensuring compliance with training requirements and effective communication with stakeholders.
Highest-signal resume keywords
Clinical Research ExperienceClinical Trial MethodologiesTeam LeadershipStakeholder CommunicationFluency in English
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchClinical Trial MethodologiesStudy DesignSite IdentificationSite SelectionPre-Feasibility AssessmentCompliance ManagementData AnalysisProject ManagementRegulatory Knowledge
Soft Skills
Team ManagementRelationship BuildingEffective CommunicationProblem SolvingAdaptability
Certifications & Qualifications
BS/BSc/MS/MScPhD/MD
Industry Keywords
CROsGSSO StrategiesClinical TrialsStakeholder EngagementGlobal Travel
About the role
Key responsibilities & impact- Oversee job functions as described in the relevant job descriptions and ensure compliance with training requirements.
- Responsible for country level input into country selection, pre-feasibility, study design and site identification and selection.
- Ensure that feedback on country/site decisions is effectively communicated to appropriate stakeholders.
- Establish consistent direction and priorities across assigned countries/cluster/region.
- Develop relationships with the CROs/vendors locally in support of delivery of GSSO strategies.
Requirements
What you’ll need- BS/BSc/MS/MSc or equivalent and extensive clinical research experience.
- PhD/MD or equivalent and extensive clinical research experience.
- Extensive knowledge (minimum 8 years) of clinical trial methodologies.
- Ability to lead and manage diverse teams.
- Availability to travel within the region and/or globally as required.
- Must be fluent in English. Local language capabilities are an advantage.
Benefits
Comp & perks- Health benefits to include medical, prescription drug, dental and vision coverage.
- 401(k) plan with Pfizer Matching Contributions.
- Additional Pfizer Retirement Savings Contribution.
- Paid vacation.
- Paid holiday and personal days.
- Paid caregiver/parental and medical leave.