Laxmi Maurya Email & Phone Number | - Global Clinical Research Industry Experience, Phase I-IV trials – Vast experience in Site Recruitment Visits, Pre-Study Site Initiation Visits (PSSVS), Site Initiation Visits (SIVS), routine/interim (RMVs/IMVs), close-out (COVs) and assisted in FDA Audits and Sponsor Audits. - Facilitating Investigator Meetings, Presentations, and Seminars, Protocol Writing, Developing Budgets, CRFs, SOPs and Training Material for Sponsors. - Contracting and negotiation with third party vendors such as CROs, Labs, Data Management team. - Training In-house team & draft study designs, protocols and CRFs, feasibility with CROs. - Responsible for accurate and timely Data Collection, Documentation, Raising Queries and Reporting - Proven ability to work both independently and in a team environment as project/study resource to ensure goals and deadlines are met within company/FDA regulatory guidelines. - Maintaining, Documenting & Conducting the Quality Assurance and Review of TMF and Site Files.

Laxmi Maurya

- Global Clinical Research Industry Experience, Phase I-IV trials – Vast experience in Site Recruitm...
New York, New York, United States

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Laxmi Maurya’s Email laxmi@ivericbio.com

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Laxmi Maurya’s Location New York, New York, United States

Laxmi Maurya’s Current Industry Astellas Pharma

Laxmi Maurya’s Prior Industry Iveric Bio | Cliantha Research | Clinuvel Pharmaceuticals | Velocity Pharma | Victoria Hospital

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Senior In-house CRA

2024-03-01 00:00:00 - Present

Sr. Clinical Research Associate

2020-03-01 00:00:00 - 2024-03-01 00:00:00

In-house Clinical Research Associate

2018-10-01 00:00:00 - 2019-10-01 00:00:00

In-House Clinical Research Associate

2014-01-01 00:00:00 - 2016-07-01 00:00:00

Clinical Research Associate

2011-01-01 00:00:00 - 2013-01-01 00:00:00

Clinical Research Coordinator

2007-09-01 00:00:00 - 2009-10-01 00:00:00

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Laxmi Maurya is a - Global Clinical Research Industry Experience, Phase I-IV trials – Vast experience in Site Recruitment Visits, Pre-Study Site Initiation Visits (PSSVS), Site Initiation Visits (SIVS), routine/interim (RMVs/IMVs), close-out (COVs) and assisted in FDA Audits and Sponsor Audits. - Facilitating Investigator Meetings, Presentations, and Seminars, Protocol Writing, Developing Budgets, CRFs, SOPs and Training Material for Sponsors. - Contracting and negotiation with third party vendors such as CROs, Labs, Data Management team. - Training In-house team & draft study designs, protocols and CRFs, feasibility with CROs. - Responsible for accurate and timely Data Collection, Documentation, Raising Queries and Reporting - Proven ability to work both independently and in a team environment as project/study resource to ensure goals and deadlines are met within company/FDA regulatory guidelines. - Maintaining, Documenting & Conducting the Quality Assurance and Review of TMF and Site Files.

Laxmi Maurya has prior
experience in the following industries:
Iveric Bio | Cliantha Research | Clinuvel Pharmaceuticals | Velocity Pharma | Victoria Hospital

Laxmi Maurya has the following professional experience:
Astellas Pharma | Iveric Bio | Cliantha Research | Clinuvel Pharmaceuticals | Velocity Pharma | Victoria Hospital