ClinVice Training Academy provides a comprehensive program that equips Principal and Sub-Investigators with the essential knowledge and leadership skills needed to oversee clinical trials effectively.
The training covers Good Clinical Practice (GCP), research ethics, protocol design and interpretation, patient safety oversight, regulatory obligations, and leadership skills for managing site teams.
ClinVice CRC Academy focuses on building operational excellence at the clinical site level.
Trainees learn trial coordination, regulatory documentation management, patient recruitment strategies, data entry accuracy, and query resolution, ensuring sites are audit-ready at all times.
ClinVice CRA Academy focuses on site monitoring, visit planning, compliance verification, reporting, and effective site communication.
Trainees gain critical skills for ensuring that studies adhere to protocols and regulatory requirements.
This program provides a comprehensive foundation in clinical research for professionals seeking to advance their careers or transition into specialized roles.
Training covers clinical trial lifecycle, regulatory frameworks, GCP compliance, site and sponsor interactions, protocol adherence, and advanced operational strategies.
It is designed to build well-rounded professionals capable of excelling in multiple aspects of clinical research.
• Beginner : Overview of clinical trials, roles in research, GCP fundamentals, and protocol basics .
• Advanced : Multi-study oversight, regulatory compliance, leadership skills, and risk management strategies .
This program is designed for pharmacists involved in clinical trials, covering Investigational Medicinal Product (IMP) handling, storage, labeling, accountability, and adherence to trial protocols .
A hands-on program that trains entry-level professionals to provide essential support to clinical trial operations, including document management, trial master file (TMF) maintenance, logistics coordination, and site communication .
This advanced training builds leadership and project management skills required to lead clinical trials.
It covers project planning, budgeting, team leadership, vendor oversight, risk management, and cross-functional communication.
This program trains participants in writing protocols, Investigator Brochures (IBs), Clinical study reports (CSRs), informed consent forms (ICFs), other clinical trial regulatory documents, and peer-reviewed manuscripts, while also developing skills to communicate scientific data effectively .
This program develops strong capabilities in the design, management, and analysis of clinical trial data .
Trainees learn eCRF design, database build, data cleaning, query resolution, coding (MedDRA, WHO Drug), statistical analysis plans (SAPs), and generation of final tables, listings, and figures (TLFs) .
The course also covers compliance with CDISC and global data standards .
This course prepares participants to master clinical trial submission processes, IRB/EC coordination, and navigating country-specific regulatory requirements, streamlining approvals and reducing start-up delays .
Targeted workshops that update clinical research professionals on evolving global regulations and best practices .
Participants gain hands-on skills in GCP compliance, implementing ICH-E6(R3), preparing for audits, and adopting risk-based monitoring techniques .
ClinVice designs bespoke training solutions tailored to the unique needs of pharmaceutical companies, CROs, and clinical sites.
These programs can combine multiple modules, incorporate company SOPs, and be delivered virtually or on-site.
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