More jobs:
Site Management Lead
Job in
Florham Park, Morris County, New Jersey, 07932, USA
Listed on 2026-09-21
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-09-21
Job specializations:
-
Science
Clinical Research
Job Description & How to Apply Below
The SML provides direction and operational expertise for Clinical Site Management (CSM) integrity, quality, and timeliness of activities in assigned studies. May serve as overall CSM functional study strategy leader and/or manage area site execution activities.
Responsibilities:- Drive global and/or area-level CSM deliverables by targeted timelines with allocated resources.
- Analyze study timelines/assumptions to confirm CSM deliverable feasibility; support/communicate CSM resource needs with Country Leaders.
- Own study-level site monitoring strategy (Site Monitoring Plan) and set/lead Site Engagement Strategy.
- Maintain study/area timelines across the lifecycle; drive site activities (selection, activation, engagement, protocol adherence, close out).
- Oversee monitoring activities to ensure quality deliverables, status tracking, milestone adherence, and acceleration; align data snapshots/database locks to Data Cleaning Plan; ensure site closure (Site Closure Plan).
- Proactively identify, evaluate, and mitigate risks; key contributor to RAMP.
- Collaborate with Clinical Study Team stakeholders to manage risks; ensure site compliance, elevate issues, and analyze trends for continuous improvement.
- Provide inputs on expected study-level CSM documents and drive TMF completeness for CSM artifacts.
- Ensure ongoing CSM Inspection Readiness activities are completed from study start to close.
- Bachelor’s degree or equivalent OUS degree in (para) medical or scientific field.
- 5+ years industry clinical research experience, including 2 years monitoring or project management/global study experience.
- Preferred: initiation through completion across multiple phases (Phase II/III; Phase I in patients); multiple therapeutic areas/disease indications.
- Core competencies in clinical trial management; strong communication and leadership; ability to influence without authority in a matrix.
- Competence with SOPs, ICH, global regulations, ethics/compliance.
- Excellent written/verbal English communication; planning/organizational skills; works autonomously and in team.
- Strong presentation skills; advanced Microsoft Word/PowerPoint/Excel/One Note.
- paid time off (vacation/holidays/sick)
- medical/dental/vision insurance
- 401(k)
- long-term incentive program eligibility.
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×