Laxmi Maurya

FAQ About Laxmi Maurya

• What is Laxmi Maurya's address?

  Laxmi Maurya is located at
  New York, New York, United States

• What is Laxmi Maurya's job title?

  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. Astellas Pharma

• What industry does Laxmi Maurya currently work in?

  Laxmi Maurya currently works in the
  Astellas Pharma

• What is Laxmi Maurya's area of expertise?

  Laxmi Maurya specializes in
  - 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.

• Which languages does Laxmi Maurya speak? 

  Laxmi Maurya speaks the following languages:
  No languages available.

• Which industries has Laxmi Maurya previously worked in?   

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

• What is Laxmi Maurya’s work experience?  

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

• How can I find Laxmi Maurya on LinkedIn?  

  You can view Laxmi Maurya’s
  LinkedIn profile at LinkedIn URL.

• What are Laxmi Maurya’s work email addresses?  

  Laxmi Maurya’s work email addresses are
  [email protected].

• What company does Laxmi Maurya work for?  

  Laxmi Maurya works at
  Astellas Pharma