Our team is experienced in providing service in all phases of clinical development for pharmaceutical, medical device and functional food trials. We provide a full-service concept offering the entire study team for all functions, or professionals working as a part of the customers’ study team.Read More
Crown CRO has expanded its own services offering to include Data Management and Biostatistics, with its newly implemented Data Services Function. A vital part of the clinical trials life cycle, Data services has the capability to operate on a Global level for trials of any size.Read More
A new level of customer attention, flexibility and reliability is brought to you by Crown CRO from early regulatory consulting all the way to medical device trials and CE-mark and 510(k) submissions.Read More
Crown CRO Quality Assurance Services can support you to develop, implement and update your quality systems and procedures to conform to current guidelines and regulations. We also provide auditing services to help you identify your strengths, as well as areas that need improvement.Read More
Meeting clinical study or post-marketing pharmacovigilance (PV) obligations is a key requirement for your company. If you need resources or know-how, the Crown CRO PV team can offer personalized services either to strengthen your own PV functions or as a full-service PV solution.Read More
Do you need high quality translations for your clinical trials, drug regulatory affairs or pharmaceutical marketing? Crown CRO Medical Translations can offer you all of those and much more. Go to our Medical Translations page for more information and contact details.Read More
Our Regulatory Affairs function supports your goals by providing a broad variety of flexible and cost-effective Regulatory Affairs services. Our main services cover clinical trial application submissions, regulatory strategies and documentation as well as regulatory procedures for pharmaceuticals and medical devices.Read More
Crown CRO supports pharma and biotech companies and other CROs with study rescue operations. A fresh point of view, new ideas or simple support and motivation can help to put the study back on track and bring it to a successful conclusion.Read More
We have performed trials in all phases of clinical development. We have played various roles in our projects from managing full-service trials and programs globally and regionally. We can also support in regional parts of the trials, as well as providing resources and ad hoc services in our countries. We also provide Study Rescue Services.
The local knowledge of our experienced team is what is behind of our success. The knowledge of local regulatory processes combined with a wide network of investigators and Key Opinion Leaders enables us to successfully complete our commitments to our customers.
We provide our professionalism, in-depth experience and service-oriented way of working to focus on delivering the high quality data on time and within budget.
Our 125+ professionals are located in our offices in Finland, Sweden, Denmark, Norway, Estonia, Latvia and Lithuania. Our operations also cover Iceland, Belarus, Belgium and Georgia. We also have a worldwide network of partners.
Crown CRO provides services in the pharmaceutical, biotechnology, functional food and medical device sectors, as well as to other contract research organizations. Our services also cover quality assurance, pharmacovigilance, regulatory, and translation services.
We have been involved in over 900 clinical studies in more than 18 countries in various therapeutic areas and in all phases of clinical development. We currently have 100 active clinical trials ongoing.
Our vast experience enables us to serve our customers in coordinating trials from early phases up to late phase and real-world studies with high quality data and on time delivery within budget.
Our mission is to deliver top quality services to our customers while providing an ideal working environment for our employees.
As a Clinical Project Manager and a Lead-CRA, you will be expected to deliver high quality clinical study data throughout clinical trials from study start to closure. You will contribute to the overall success of Crown CRO and its customers by establishing and sharing competence and expertise on co-ordination of study tasks, strategic therapeutic fields and good customer relations.Read more
Adial Pharmaceuticals, Inc. (NASDAQ: ADIL; ADILW), a clinical-stage biopharmaceutical company focused on the development of treatments for addiction, today announced that it has commenced a Phase 3 pivotal clinical trial to investigate AD04 as a genetically targeted therapeutic agent for the treatment of Alcohol Use Disorder (AUD). The trial has initially started in Finland, where Adial previously announced it had received approval to commence the trial. The trial is also expected to be conducted in Sweden, Poland, Latvia, Estonia, Croatia, and Bulgaria. Adial has filed clinical trial applications (CTAs) to also conduct the trial in each of these countries where additional trial sites will be initiated on a country-by-country basis following each CTA approval.Read more
Valitettavasti joudumme perumaan toukokuulle suunnitellut CRA-koulutuksen COVID-19 tilanteen vuoksi. Koulutukseen ilmoittautui runsaasti väkeä, joten olemme päättäneet järjestää ensi syksynä kolme erillistä CRA-koulutustapahtumaa. Kiitämme lämpimästi kaikkia koulutukseen ilmoittautuneita. Kaikki koulutukseen ilmoittaneet tulevat saamaan sähköpostitse tiedot tulevista koulutuspäivistä syksyllä ja mahdollisuuden ilmoittautua niille.
Crown CRO järjestää toukokuussa kaksi CRA-koulutusohjelmaa.
Koulutus tarjoaa sinulle
• Kattavat perustiedot kliinisistä tutkimuksista ja niiden toteuttamisesta
• Runsaan tietopaketin CRA:n työstä ja sen sisällöstä tutkimuksen eri vaiheissa
• Hyvät teoreettiset valmiudet hakeutua CRA:n työhön
• Aitiopaikan tutustua CRA:n työhön kokemusasiantuntijoiden opastuksella
• Ainutlaatuisen tilaisuuden suorittaa Crown CRO:n GCP-testi koulutuksen päätteeksi
Koulutuspaikkojen määrä on rajallinen, joten varaa oma paikkasi pian!Read more
As a Sr.CRA, you will be expected to deliver high quality clinical study data throughout clinical trials from initiation to closure. You will contribute to the overall success of Crown CRO and its customers by establishing and sharing competence and expertise on co-ordination of study tasks, strategic therapeutic fields and good customer relations.Read more
Building a better and healthier tomorrow is a goal shared by the entire world. We at Crown CRO are proud to do our part for achieving this important goal by, for example, sharing our skills and knowledge and promoting the entire industry.
One way to do this is to help new, talented people enter the field. This is also one of the driving forces behind our new CRA training program, which we launched this spring. Being strong believers in continuous professional development, we have previously organized CRA training in-house. Now, for the first time, we have opened up the program to people outside the company, too. Read more
Part of our mission at Crown CRO is to bring to market new, safer, and more effective medications, improve treatment outcomes, help advance medicine and, ultimately, create a healthier future. That is why we also wholeheartedly support the recent appeal for the new government to improve the conditions and resources for clinical research. The appeal was signed by 33 individuals and organizations involved in clinical research, including Pharma Industry Finland PIF. Crown CRO has been a PIF member since 2005.Read more
Crown CRO OyVaisalantie 4 FI-02130 Espoo Finland Tel. +358 9 8870 0500 Fax +358 9 8870 0599
General business opportunity and collaboration enquiries:
Päivi Itkonen, Acting Chief Executive Officer