ALCOVIA STANDS FOR
HEALTH CARE

Alcovia is a site management organization (SMO) which also provides online courses for candidates and job placement services for clinical research organizations.

Site Management Organization

Online Courses & Job Placements

ALCOVIA: Cultivating Excellence in Clinical Research

ALCOVIA, a leader in clinical research, offers top-tier site management and educational courses. We link students with strong academic records to advanced careers through our innovative online courses and effective job placement services, setting new standards in the industry.

About Us

ALCOVIA is provides site management organization (SMO) and online courses & Job Placements services

We are a streamlined organization that ensures immediate customer response and the flexibility to make adjustments rapidly, providing consistent quality and the first-hand attention from a senior, experienced team. We believe this paradigm allows us to provide our customers with a level of service that is flexible, efficient and sustainable for the delivery of a portfolio of clinical trials. We strive to establish synergies and team chemistry, and develop successful relationships that consists of a shared vision, mutual trust, and complementary expertise. ALCOVIA focuses on understanding and fulfilling our customers needs and delivering top-quality results within aggressive timelines.

Add best skills and knowledge to your career with less fee and time.
Well experienced staff worked in MNC companies.
Internships availabilities.

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Our Insights In SMO & Online Courses


ALCOVIA is fully provide online courses like a CDM, PV, SAS, CRA, Regulatory affairs and English and soft skills with well experienced staff.

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ALCOVIA Clinical Research Online courses

An SMO is a company that provides clinical trial management services to pharmaceutical, biotech, or medical companies. SMOs help sponsors streamline their administrative processes while ensuring that all regulatory requirements are met.

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ALCOVIA
SMO

Site Management Organization Services

The SMO is primary that provides clinical trial management services to pharmaceutical, biotech, or medical
companies. SMOs help sponsors streamline their administrative processes while ensuring that all regulatory
requirements are met. They also support CROs and clinical investigators at the site with start-up,
monitoring, and closeout responsibilities.

Locations:

Karnataka

Tamil Nadu

Andhra Pradesh

Telangana

Type of Clinical Trials Being Conducted:

Phase II

Phase III

Phase IV

Device Studies

What are the benefits of working with ALCOVIA (SMO)?

The SMO can reduce trial timelines and costs and lead to more efficient and accurate trial results through a full range of services including:

ALCOVIA: Clinical Research Online courses & Placements

ALCOVIA fully provide online courses for corporate and pharmaceutical and other sectors with well experienced staff, ALCOVIA is committed and full fill student’s dreams and requirements during training. ALCOVIA focus on quality of courses and job placement at the earliest time period

Clinical Research online courses & Job Placements

Pharmaceutical Industries Courses & Job placements

National & International Trainers

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Total Enrolled Students

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Total Job Placements

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Why Choose Alcovia?

Expert trainers and well experienced their respective departments.

International trainers

Focus on all therapeutics areas including Oncology trials courses.

ALCOVIA have strong bonding with Sponsors, Pharmaceuticals industries & CRO”s.

ALCOVIA Track and ensure feedback & reviews comments for every activities.

ALCOVIA have runs own SMO sites on across India.

ALCOVIA Make you the best resource for companies.

The SMO is a primary organization that provides clinical trial management services to pharmaceutical, biotech, or medical companies. Identifying and/or managing investigators and sub-investigators.Managing and fulfilling staff requirements and recruitment.Preparing Institutional Review Boards (IRB) Assisting with trial start up, site initiation, and closeout operations.Brings more trials to the physicians.On time documentation like e-CRF, source documents.Coordination with CRA’s and vendors.

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