Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Clinical Research Associate (M/W) - Location: Belgium

Company: Chiltern
Location:
Reference: GQ18781
Closing Date: 31 Dec 18
Type: Full Time
Salary (£): Competitive
Benefits:

Job Summary:

CRA positions in Belgium - Home-based or Office-based

Requirements:

Covance is currently looking for seasoned Clinical Research Associates to join our team in Belgium. Many opportunities are offered to you, either within our Flexible Solutions department dedicated to one sponsor/client or within our clinical operations department. We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials.

Requirements:

As a Clinical Research Associate you will lead all aspects of study site monitoring according to Covance SOP, ICH guidelines and GCP. You will take part in pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.

You will become a part of our team who is always ready to help. We offer flexibility and the possibility for you to work either office-based or home-based as well as the possibility to devote all your professional skills and knowledge into monitoring investigational sites as we organize our work environment and responsibilities with high standards.

Our sponsors invest heavily in training and crafts modern system of Clinical Trials so if you are passionate about working with an outstanding team and expand your horizons feel free to reach us.

Responsibilities include:

All details of site management as prescribed in the project plans

Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks

Negotiation of study budgets with potential investigators and collaboration with Covance legal department with statements of agreements

Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.

Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems


Education / Qualifications

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)

Fluency or excellent knowledge of the three following languages: Dutch, French and English

 

Experience

Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines

Excellent understanding of Serious Adverse Event (SAE) reporting

Ability to resolve project-related problems and prioritize workload for self and team

You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).

 

Apply for this job: Clinical Research Associate (M/W) - Location: Belgium

Contact Information:

Address:  Germany
Norsk-Data-Strasse 1, 61352 Bad Homburg v.d.H. Germany

Germany
Tel:  +49 6172 9443 0
Fax:  +49 6172 9443 300
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.