Stan Duitsman
- Role
- Senior Clinical Trial Manager at ICON plc
- Location
- Olathe, KS, US
- LinkedIn followers
- 500 followers
About Stan Duitsman
Degrees/Certifications: B.S, B.A, Expert GCP Barnett Accreditation, NASM CES, NASM PES,…
Experience
Senior Clinical Trial Manager
Mar 2023 — Present
Primary point of contact for the clinical aspects of designated projects and responsible for developing successful cross-functional relationships with internal and external stakeholders.\\\\n- Responsible for planning, scheduling and implementing the clinical aspects of projects in line with contract and budget.\\\\n- Responsible for driving enrolment as per contracted timelines.\\\\n- Regular oversight of key clinical metrics including but not limited to: Days on Site (DOS), Monitoring Visit Report (MVR) and Follow up Letters (FUL) timelines, Action Items (AI) and other quality metrics, to ensure they are met and followed-up as necessary.\\\\n- Oversight of visit report review and approval, including site issue escalation and resolution.\\\\n- Contribute to the development and maintenance of all clinical elements of cross-functional project plans.\\\\n- Responsible for coordinating and managing the clinical project team.\\\\n- Responsible for documenting clinical risks and developing mitigation strategies and associated action plans, including issue escalation and resolution.\\\\n- Responsible for the development and maintenance of operational plans for clinical deliverables.\\\\n- Ensure the core clinical portions of the Trial Master File (electronic or paper TMF) are up-to-date and maintained in accordance with SOPs and the File Master Plan (FMP). This includes documented QC checks of in house investigator site files.\\\\n- Ensure all close-out activities are completed as necessary.\\\\n- Lead and/or actively participate in the conduct of clinical team meetings.\\\\n- Ensure timely dissemination of information on study progress or issues and/or processes to all team members related to clinical deliverables and accurate tracking of any relevant study information related to clinical deliverables.\\\\n- Implement QC activities, ensure compliance with quality measures and monitor required quality metrics.\\\\n- Participate in business development activities such as bid defense meetings.\\\\n \\\\n\\\\n \\\\n \\\\n\\\\n \\\\n
Skills
- Personal Training
- Ich-Gcp
- Chemistry
- Website Management
- Clinical Site Monitoring
- Contract Management
- Social Media Marketing
- Fitness
- Baseball
- Writing
- Ap Style
- Indesign
- Editing
- Biology
- Clinical Trials
- Sales
- Conducting Interviews
- Microsoft Office
- Copy Editing
- Aseptic Technique
- Statistics
- Regulatory Compliance
- Feature Articles
- Publications
- Calculus
- Marketing
- Website Administration
- Advertising
- Customer Service
- Press Releases
- Photoshop
- Organic Chemistry
- Microbiology
- Management
- Proofreading
- Social Media
- Sports Writing
- Media Relations
- Feature Writing
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