Related News
-
ENTREPRENEURIAL CULTURE 'IMPORTANT FOR BIOTECH
The recipe for biotechnology cluster success is one which has prompted much discussion and...
-
PHARMACEUTICAL INDUSTRY BRINGS HOPE TO MS
The first tablets for treating multiple sclerosis (MS) could be available to sufferers from next...
-
-
ENTREPRENEURIAL CULTURE 'IMPORTANT FOR BIOTECH
The recipe for biotechnology cluster success is one which has prompted much discussion and...
-
PHARMACEUTICAL INDUSTRY BRINGS HOPE TO MS
The first tablets for treating multiple sclerosis (MS) could be available to sufferers from next...
CRA /Warsaw
| Category | Clinical Research |
|---|---|
| Job Ref | MN/HQ00013927 |
| Job Type | Permanent |
| Salary | Salary on application - Excellent salary |
| Location | Poland - Warsaw |
18 Jul 2010
My client is the largest R&D company which carries out clinical research in Central Europe. The company's clients include global pharmaceutical companies which outsource clinical research to contract research organizations.
Currently they are looking for 2 experienced candidates for the position of Clinical Research Associate /oncology - Warsaw
1 CRA - home-based
1 CRA - office-based
Summary of Job Specification
Conducts site monitoring of clinical research studies according to Standard Operating Procedures and GCP Guidelines
Job Duties and Responsibilities:
- Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaising with vendors
- Conducts feasibility work
- Monitors Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
- Independently performs CRF review; query generation and resolution against data review guidelines
Travel Required:
- Available for travel from 50% to 80% of the time, including overnight stays as necessary, consistent with project needs and office location.
- Ability to drive and have a valid driver's license.
Education / Qualifications Required
- University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
- Knowledge of GCP, monitoring procedures, basic understanding of regulatory requirements.
Experience / Skills Required:
- Minimum of two years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits).
- Ability to monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP.
- Good planning, organization and problem solving abilities.
- Ability to work with minimal supervision.
- Good communication and interpersonal skills.
- Good analytical and negotiation skills.
- Computer competency.
- Fluent in local office language and in English, both written and verbal.
Applications including CV and cover letter in English should be sent to
marek.nadolnik@hayspharma.com
In your application please put the following statement
I hereby agree for processing the following personal information strictly for the purposes of job recruitment in accordance with the regulation for the protection of personal data passed on the following day 29.08.97r. Dz.U nr 133 poz. 883.
For further information please contact
Marek Nadolnik
Email: marek.nadolnik@hayspharma.com
Services advertised by Hays Pharma are those of an Agency and/or an Employment Business
