|
Announcement |
September 6, 2004
We have launched our new website.
|
|
|
News & Events |
January 30, 2009
Experienced CRAs required starting from Fall 2009. More info |
|
|
We are committed to provide high-quality, cost effective and timely clinical research
support services to the pharmaceutical, biotechnology industries and CROs.
Please do not hesitate to contact us if the below list does not answer your questions
or you need further information about available services or opportunities for
cooperation between our organizations. We would like to help your organization to succeed and growth.
CRA.pl Team
Our Services:
1. Subcontracting
CRA.pl is willing to support your organization in field of the clinical research by:
* Outsourcing your organization in monitoring of the research project,
* Temporary subcontracting of the monitoring of limited research centers
in case of unexpected drop of your own research capacity or short term increase of the workload.
2. Trial Management
CRA.pl has capacity to manage your trial project and provide following services:
* Selection appropriate research centers and maintenance of good relationships with
clinical coordinators and centers' managers,
* Coordination of work if the project is monitored by freelancing CRAs,
* Monitoring of the performance of CRAs involved in the project,
* Providing appropriate means to the project staff to achieve projects' goals and objectives.
3. Contract Hires
CRA.pl offers your organization short and long term CRAs to boost your own research
capacity or match the staff shortage caused by employee's leaves (sick and maternity leaves,
sudden change in employee's career).
CRA.pl can share its workforce with foreign CRO, which may not wish to be formally present in Poland.
4. Business and Administration Support
CRA.pl offers administrative support in running clinical trials for organizations which are not present in Poland though:
* Assistance in registration and managing of the foreign organization in Poland,
* Assistance in managing hiring process of new staff members or freelancing CRAs,
* Acting as liaison office of a foreign CRO running trial project in Poland.
5. medical reviewer / medical monitor
* safety (AE/ SAE) processing and reporting - including writing narratives,
* quality review of medical consistency of data entered into eCRFs,
* medical guidance and staff training in relation to relevant therapeutical and disease areas,
* providing medical support for monitoring structure.
|
|
