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Available data points
Metadata
company_id
12743888
source_id
12606905
unique_domain
1
unique_website
1
last_updated_at
2025-04-06
created_at
2019-04-08
description
We use an elephant family as symbolism as their families depend on the senior female, the matriarch, to share her experience for their success. Gaea is an agile, flexible, full-service CRO with only experienced staff. As example, unlike large CRO our national CRAs in each country have 10+ years of experience. I use my long experience to lead the Gaea teams to bring a Sponsor’s clinical trial to a timely, cost-effective completion, with quality at the core. A sponsor’s trial will always get my attention as CEO. We allocate a Trial Manager or a Project Manager according to project size and this is the go-to person for the qualified providers (vendors) and the Sponsor, so keeping all communication direct and fast. We have a good network of medical experts when we need advice . Larger CRO feasibility is superficial, but we care about enrolment as slow trials cost Sponsors more money and we base our assumptions for enrolment from experts in the disease. Gaea has a good network of relevant medical specialist we ask for advice. Our HQ is in Tallinn, in digital Estonia. We are highly digitalised, including with Veeva Vault. We run Phase I – III drug trials and in all of Europe, UK, USA, Ukraine, and Georgia, with a partner in Bangladesh with its huge population. We also work in devices where EU regulation is still evolving and have great statistical expertise to call on for novel cost saving approaches such as adaptative design investigations. Quality and data management are within Gaea, and we have our qualified service providers, for such as PV: this approach means we can supplement Sponsors’ existing services with our own as they need. Our expertise is in hospital-originated interventions. We work with limited populations, oncology populations, neurology, respiratory, moving into intensive care populations: ARDS and sepsis trials that can enrol over 24/7 and require a committed, experienced CRO team.
type
Privately Held
industry_group_1
Pharmaceutical
Firmographics
company_name
Gaea OÜ Clinical Contract Research Organization (CRO)
is_b2b
1
industry
Pharmaceutical Manufacturing
founded_year
2018
size_range
11-50 employees
employees_count
7
Locations
hq_country
Estonia
hq_country_iso2
EE
hq_country_iso3
EST
hq_location
Tallinn, Harjumaa, Estonia
hq_full_address
*******
Follower counts & changes
followers_count_professional_network
440
Company websites and social media
website
https://www.gaeaou.com
professional_network_url
https://www.professional-network.com/company/gaeaou
financial_website_url
https://www.financial-website.com/organization/gaeaoü
Website traffic
total_website_visits_monthly
723
visits_change_monthly
72.97
bounce_rate
42.53
pages_per_visit
3.02
average_visit_duration_seconds
42
Employee review score & changes
company_employee_reviews_aggregate_score
-0.10000000149011612
JSON data sample
{ "company_id": 12743888, "source_id": "12606905", "company_name": "Gaea OÜ Clinical Contract Research Organization (CRO)", "company_name_alias": [ "gaea oü clinical contract research organization (cro)", "gaeaoü", "gaea (estonia)", "gaea o" ], "company_legal_name": null, "company_logo": "/9j/4AAQSkZJRgABAQAAAQABAAD/2wBDAAMCAgMCAgMDAwMEAwMEBQgFBQQEBQoHBwYIDAoMDAsK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\r\nR6CjaPQUUUASKBtHHaiiigD/2Q==", "website": "https://www.gaeaou.com", "professional_network_url": "https://www.professional-network.com/company/gaeaou", "twitter_url": [ "https://www.twitter.com/themesaxiom" ], "discord_url": [], "facebook_url": [ "https://www.facebook.com/axiomthemes-505060569826537" ], "instagram_url": [ "https://www.instagram.com/axiom_themes" ], "pinterest_url": [], "tiktok_url": [], "youtube_url": [], "github_url": [], "reddit_url": [], "financial_website_url": "https://www.financial-website.com/organization/gaeaoü", "stock_ticker": [], "is_b2b": 1, "industry": "Pharmaceutical Manufacturing", "sic_codes": [ "80", "807" ], "naics_codes": [ "62", "621" ], "categories_and_keywords": [ "healthcare", "industry: n/a", "devices", "phase iii", "dpo", "cro", "clinical trial planning", "clinical trial", "cra", "clinical research", "project management", "regulatory", "site selection", "contracts", "screening eligibility assessment", "monitoring", "biostatistics", "safety management", "medical monitoring", "quality assurance", "clinical reports", "patient recruitment", "clinical research organisation", "contract research organisation", "phase i", "phase ii", "central and pk labs management", "dsmb", "idmc", "global", "study start-up", "consent", "assent in incapacitated patients", "crf design", "data management", "clinical strategy", "clinical operations (monitoring and site management)", "risk-based quality management", "regulatory affairs", "medical writing", "site payments", "clinical trials", "digital software", "clinical project management", "data security", "health care" ], "description": "We use an elephant family as symbolism as their families depend on the senior female, the matriarch, to share her experience for their success. Gaea is an agile, flexible, full-service CRO with only experienced staff. As example, unlike large CRO our national CRAs in each country have 10+ years of experience. I use my long experience to lead the Gaea teams to bring a Sponsor’s clinical trial to a timely, cost-effective completion, with quality at the core. A sponsor’s trial will always get my attention as CEO. We allocate a Trial Manager or a Project Manager according to project size and this is the go-to person for the qualified providers (vendors) and the Sponsor, so keeping all communication direct and fast. We have a good network of medical experts when we need advice . Larger CRO feasibility is superficial, but we care about enrolment as slow trials cost Sponsors more money and we base our assumptions for enrolment from experts in the disease. Gaea has a good network of relevant medical specialist we ask for advice. Our HQ is in Tallinn, in digital Estonia. We are highly digitalised, including with Veeva Vault. We run Phase I – III drug trials and in all of Europe, UK, USA, Ukraine, and Georgia, with a partner in Bangladesh with its huge population. We also work in devices where EU regulation is still evolving and have great statistical expertise to call on for novel cost saving approaches such as adaptative design investigations. Quality and data management are within Gaea, and we have our qualified service providers, for such as PV: this approach means we can supplement Sponsors’ existing services with our own as they need. Our expertise is in hospital-originated interventions. We work with limited populations, oncology populations, neurology, respiratory, moving into intensive care populations: ARDS and sepsis trials that can enrol over 24/7 and require a committed, experienced CRO team.", "description_enriched": null, "description_metadata_raw": "GaeaOÜ is an agile full-service CRO in Phase I – III, IIT in all of Europe, with partners in the USA and Australia Read more Agile full-service CRO Commissioned by Sponsors, Gaea Trial Acceleration identifies and addresses the issues at sites, that are blocking their enrolment Read more Trial Enrolment Accelerator The GaeaOÜ CEO will work in-house at a company to define the clinical strategy and execute it with the company’s choice of CRO Read more Clinical Trial Planning", "type": "Privately Held", "status": { "value": "active", "comment": null }, "founded_year": "2018", "size_range": "11-50 employees", "employees_count": 7, "followers_count_professional_network": 440, "followers_count_twitter": null, 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}
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