Site Activation Manager
Syneos Health
Posted: 10/19/2026
IT Service Manager
itecor
Posted: 10/14/2026ITSM
Site Manager – Data Centers
INP Schweiz AG
Posted: 10/12/2026
Manager, Laboratory Systems – Data
Johnson & Johnson
Posted: 10/8/2026CloudCyber SecurityServiceNow
Manager, Laboratory Systems – Data
Johnson & Johnson
Posted: 10/8/2026CloudCyber SecurityServiceNow
Market Access Manager
Sobi - Swedish Orphan Biovitrum AB (publ)
Posted: 10/8/2026
Private Travel Manager, German Speaking
Ten Lifestyle Group
Posted: 10/8/2026
Technical Manager
A-ROSA REEDEREI GMBH
Posted: 10/7/2026
Area Manager – Jewellery
GUESS?, Inc.
Posted: 10/7/2026
Transformation Manager
ABB
Posted: 10/6/2026
Contract and Claims Manager, m/f/d
Axpo Group
Posted: 10/5/2026
Global Commercialization Manager
Agilent Technologies
Posted: 10/2/2026
Incident & Problem Manager
SIX
Posted: 10/1/2026ITSM
IT Provider Manager
SBB CFF FFS
Posted: 9/30/2026
Global Sustainability Market Engagement Manager
Hitachi
Posted: 9/29/2026
Business Area Manager – Wealth Management Solutions
swissQuant
Posted: 9/23/2026
Applications Manager, Service Manager
Coopers Group AG
Posted: 9/19/2026
Partner Relationships Manager
myPOS
Posted: 9/15/2026
Manager
Bucher Invest AG
Posted: 9/15/2026Site Activation Manager
Syneos HealthCore Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing Site Start-Up processes, including regulatory maintenance, project deliverables, and clinical trial agreements. Proficient in developing integrated timelines, preparing core submission documents, and ensuring compliance with Standard Operating Procedures.
Highest-signal resume keywords
Site Start-Up ManagementRegulatory Pathways KnowledgeClinical Trial Agreements OversightCore Submission Document PreparationProject Budget Management
About the role
Key responsibilities & impact- Collaborate with major functional areas across clinical trial and business functions
- Identify and evaluate Site Start-Up issues, regulatory pathways, patient enrollment matters, and project risks
- Ensure project deliverables meet internal and customer expectations
- Develop and maintain customer relationships for assigned projects
- Provide oversight of project start-up deliverables throughout project life-cycle maintenance
- Manage regulatory maintenance activities, amendment submissions, authority and ethics committee communications, and import/export license extensions
- Oversee executed amended clinical trial agreements and investigator budgets with investigator sites
- Manage overall Site Start-Up timelines and realign plans as needed
- Develop integrated timelines and report weekly progress, including mitigation plans for timing risks and gaps
- Prepare and present Site Start-Up strategy and status at client meetings
- Review project budgets against milestones and profitability expectations; take corrective measures as needed
- Track out-of-scope work through backlog assignment
- Prepare core submission documents and clinical trial application dossiers for amendments
- Perform Regulatory Impact Assessments and oversee second-level reviews
- Assist with updates to master Subject Information Sheets and Informed Consent Forms
- Oversee collation, quality review, and submission of country-specific applications
- Contribute to Site Start-Up department change initiatives
- Submit relevant documents to the Trial Master File according to company SOPs and sponsor requirements
- Perform other assigned work-related duties
Requirements
What you’ll need- Equivalent experience, skills, and/or education will also be considered
- Ability to collaborate with Business Development, Alliance Management, Contracts and Proposals Development, SSU Country Managers, Project Management, Clinical, Data Management, and Medical Writing
- Knowledge of Site Start-Up and project regulatory pathways
- Ability to interpret complex issues and make sound business decisions
- Ability to manage project deliverables, projections, reports, updates, risks, timelines, and budgets
- Knowledge of life-cycle maintenance regulatory activities, including study maintenance and amendment submissions
- Experience overseeing clinical trial agreements, investigator budgets, competent authority and ethics committee communications, and import/export license extensions
- Ability to prepare core submission documents and clinical trial application dossiers for amendments
- Ability to perform Regulatory Impact Assessments
- Ability to develop or update Subject Information Sheets (SIS) and Informed Consent Forms (ICF)
- Ability to oversee country-specific application collation, quality review, and submission
- Ability to comply with Standard Operating Procedures, controlled document requirements, and Sponsor requirements
- Ability to use professionally recognized tools for planning and management of scope, timeline, resources, and budgets
Benefits
Comp & perks- Career development and progression
- Supportive and engaged line management
- Technical and therapeutic area training
- Peer recognition
- Total rewards program
- Inclusive culture
- Minimal travel may be required (up to 25%)
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Regulatory Maintenance ActivitiesProject Deliverables ManagementClinical Trial Application DossiersRegulatory Impact AssessmentsSubject Information Sheets DevelopmentInformed Consent Forms DevelopmentAmendment SubmissionsQuality Review ProcessesTimeline DevelopmentRisk Mitigation Planning
Soft Skills
CollaborationDecision-MakingCommunicationProblem-SolvingRelationship Management
Tools & Technologies
Project Management ToolsPlanning ToolsControlled Document Management Systems
Industry Keywords
Clinical TrialsSite Start-UpRegulatory ComplianceEthics Committee CommunicationsImport/Export License Extensions