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Job Details

Clinical Research Associate - Oncology - Belgium

Company: INC Research
Location:
Reference: 17003914
Closing Date: 13 Dec 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose: shortening the distance from lab to life.

Requirements:

We are currently looking to strengthen our Clinical Monitoring team in Belgium and are seeking a Clinical Research Associate for our Oncology Business Unit to be based from either our office in Zaventem or we can also consider regional employees.

We understand that cancer is not one disease, but a category of widely varying diseases, each with its own specialized scientific complexities, patient populations and range of treatment options. Our Oncology and Hematology practice is dedicated to the execution of clinical trials in these complex indications and is staffed by dedicated professionals with backgrounds in oncology drug development in academia, industry and CRO settings. This expertise, combined with INC Research’s Trusted Process® methodology for delivering dependable trial outcomes, provides the resources, clinical expertise and development know-how to help our clients with every facet of their Oncology research.


A brief summary of duties you will be involved in:
• Monitoring all types of clinical trials and participating in all types of site visits ensuring adherence to Good Clinical Practices, investigator integrity and compliance with all study procedures
• Data Handling, Reporting, Tracking and administrative tasks
• Performing management of study site activities to ensure the integrity of clinical data, in adherence to all applicable regulatory guidelines.

Qualifications
 

Skills and attributes:


To succeed in this role you will need the following skills/experience:
• Education - BS/BA or equivalent with solid clinical trial monitoring experience, demonstrating successful performance of CRA position
• Previous nominal practical experience in conducting clinical pharmaceutical research studies in a hospital setting, pharmaceutical company or CRO
• Basic understanding of SOPs, WIs, FDA, and local regulations as well as ICH GCP guidelines
• Good command of written and spoken English language


What happens next:
If your application is successful you will be contacted by one of our dedicated recruiters who will arrange a suitable date and time to speak to you further about this opportunity.


Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract.

Occasionally required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees.

Apply for this job: Clinical Research Associate - Oncology - Belgium

Contact Information:

Address:  INC Research Europe
Királyhágó tér 8-9, 2th floor, 1126 Budapest, Hungary
1126
Hungary
Tel:  +36 1 489 48 56
Website:  Visit Our Web Site

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