LANS Clinical Research Consulting

Clinical /Quality/ Regulatory

Services

Industries

  • Pharmaceutical

  • Medical Device

  • Biologics

Clinical, Quality, Regulatory Associate

Responsible for the design, implementation, and monitoring of clinical trials. Ensure that clinical trials are conducted in accordance with standard operating procedures, Good Clinical Practice (GCP), and guidelines meeting quality and regulatory standards. Protecting the safety and well-being of study participants.

Welcome to LANS Clinical Research.  We are here to provide you with all of your clinical research needs:

Services

  • Clinical Research  - Protocol & CSR Writing/Randomization/Blinding/Cohort Studies
  • Data Management - Data Collection/ Analysis/Adverse Event Reporting

  • Case Report Form Design

  • Regulatory-GCP/FDA/ICH Guidelines/IRB
  • Study Management - SOPs/Subject Recruitment/Informed Consent

Associate Director

Provides leadership and guidance to study teams, including mentoring and managing staff to enhance team performance and development. Develop and maintain strong relationships with key stakeholders, including external vendors, clinical sites, and regulatory bodies.

Director

Directs overall strategy and delivery of deliverables. Analyze, develop, and execute resource management modeling, inclusive of operational, financial, and administrative models..

Book an appointment

For more information or an appointment please email us at lansclinicalresearch@gmail.com.