Susan Mcdaniel Email & Phone Number
@i3global.com
2 phones found area 913
LinkedIn matched
Who is Susan Mcdaniel? Overview
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Susan Mcdaniel is listed as Open to new opportunities based in Durham, North Carolina, United States. AeroLeads shows a work email signal at i3global.com, phone signal with area code 913, and a matched LinkedIn profile for Susan Mcdaniel.
Susan Mcdaniel previously worked as Senior Project Manager at Oncobay Clinical and Senior Project Manger at Protrials Research Inc.. Susan Mcdaniel holds Mj, Health Law from Loyola University Chicago School Of Law.
Email format at i3global.com
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AeroLeads found 1 current-domain work email signal for Susan Mcdaniel. Compare company email patterns before reaching out.
About Susan Mcdaniel
I offer strong inter-active relationship and communication skills; excellence in an independent or within a team-working environment; excellent computer knowledge including Microsoft Word, Excel and Outlook, electronic data capture. In addition, 18 years of nursing experience, a degree in health law, PMP verification, and 23 years of experience in clinical research including monitoring and global clinical project management in academia, pharmaceutical industry, and CROs.
Listed skills include Clinical Data Management, Clinical Trials, Protocol, Cro, and 18 others.
Susan Mcdaniel work experience
A career timeline built from the work history available for this profile.
Senior Project Manger
Clinical Trial Manager
Clinical Trial Manager
Clinical Trial Manager at Mycovia Pharmaceuticals(Mycovia Pharmaceuticals was created from the acquisition of Viamet Pharmaceuticals by NovaQuest Capital Management.
Clinical Trial Manager
Operations Director
Senior Clinical Project Manager
Senior Clinical Project Manager
- Manage phase1-3 global clinical studies
- Responsible for the development and maintenance of regulatory documentation, site enrollment logs, status reports, clinical tracking reports, waiver logs, protocol deviation logs, and drug shipment accountability.
- Design informed consent templates, review and approve site informed consents; Develop study manuals and other study tools; author monitoring plans
In House Cra
- Perform holistic review of patient data to ensure patient safety, proactively identify potential safety signs/trends and ensure data quality. Ensure that all data and study documents are handled consistently with the.
- Identifying problems and/or inconsistencies; monitor site and subject progress, including documentation and reporting of adverse
Project Manager
- Coordinate cancer network activities for multiple studies including site start up, site initiation, patient recruitment and patient management.
- Provide network oversight for regulatory compliance, drug accountability, and data entry and validation across network sites according to institutional SOPs, GCP and ICH guidelines.
- Responsible for the development and maintenance of study documentation, including regulatory documents, study tracking logs, study manuals, status reports, and other study
Associate Director
- Function as Project Manager on project(s) and/or program(s).
- Provide oversight to the project team in the identification of potential issues and formulation of proactive plans to address these issues.
- Communication with team members and management regarding current projects.
- Manage study team to ensure that assigned projects are completed within assigned budget and timelines.
- Participate in Customer capability and proposal support meetings.
Senior Clinical Trial Manager
- Simultaneously manage multiple Phase I-Phase III global studies.
- Develop and maintain study budgets and timelines.
- Responsible for the development and maintenance of regulatory documentation, site enrollment logs, status reports, clinical tracking reports, waiver logs, protocol deviation logs, and drug shipment accountability.
- Identify and oversee the selection and management of CROs, contract labs, and other vendors
- Provide input into protocol development, Case report Forms, Clinical Study Reports, publications and other documents as assigned.
- Design informed consent templates, review and approve site informed consents; Develop study manuals and other study tools; author monitoring plans.
Susan Mcdaniel education
Mj, Health Law
Bsn, Nursing
Frequently asked questions about Susan Mcdaniel
Quick answers generated from the profile data available on this page.
What is Susan Mcdaniel's role at their current company?
Susan Mcdaniel is listed as Open to new opportunities.
What is Susan Mcdaniel's email address?
AeroLeads has found 1 work email signal at @i3global.com for Susan Mcdaniel.
What is Susan Mcdaniel's phone number?
AeroLeads has found 2 phone signal(s) with area code 913 for Susan Mcdaniel.
Where is Susan Mcdaniel based?
Susan Mcdaniel is based in Durham, North Carolina, United States.
What companies has Susan Mcdaniel worked for?
Susan Mcdaniel has worked for Oncobay Clinical, Protrials Research Inc., Dova Pharmaceuticals, Mycovia Pharmaceuticals, and Viamet Pharmaceuticals.
How can I contact Susan Mcdaniel?
You can use AeroLeads to view verified contact signals for Susan Mcdaniel, including work email, phone, and LinkedIn data when available.
What schools did Susan Mcdaniel attend?
Susan Mcdaniel holds Mj, Health Law from Loyola University Chicago School Of Law.
What skills is Susan Mcdaniel known for?
Susan Mcdaniel is listed with skills including Clinical Data Management, Clinical Trials, Protocol, Cro, Sop, Pharmaceutical Industry, Oncology, and Cancer.
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