Gentis is a Belgian recruitment company headquartered in Brussels and providing permanent staffing as well as project sourcing solutions worldwide in multiple sectors. Each of our sectors is serviced by a dedicated team of specialist recruiters, with accumulated experience of decades in recruitment.
Thanks to close collaboration with the major players in each industry and our high profile among experienced professionals in our target sectors, Gentis has grown rapidly and is now capable of meeting the multiple needs in IT, Engineering, as well as the Oil & Gas and Pharmaceutical Sectors.
Whether you are seeking a new opportunity or whether you need to recruit the best person to fill a need within your company, at Gentis our daily practice is to carry out all activities to provide you the highest quality solution in the fastest timescale.
To assure this successful solution for our clients and candidates, we deploy a wide range of candidate-acquisition tools : headhunting, job boards, databases - including our own -, social network search tools, as well as dedicated researchers specialized by sector and profession.
In addition, through the many years of practice of our recruiters and headhunters, Gentis has developed a constantly expanding worldwide network of sector professionals and client companies which we use to match requirements of our candidates and clients.
You will draft and perform maintenance of an Investigator Brochure, write protocols, reports and other study related documents for pre-clinical & clinical studies. You will prepare manuscripts for publication and posters including the performance of literature reviews.
You will perform Adverse Events narratives as well as Identification and classification of events. You will research and follow-up of safety-relevant data and do electronic documentation and quality control, including filings and version control.
You are an English native speaker of equivalent. You have a solid academic background in medical writing within pharmaceutical sciences, medical device, biotech, or equivalent. You have excellent knowledge of the respective guidelines and regulations, especially GLP-GCP and a sound knowledge of biostatistics.
You are rigorous and accurate in your work and have the ability to express complex data in a concise way. You demonstrate excellent organization and communication skills: you have the ability to work both independently and efficiently within an interdisciplinary team.
Please apply with your CV and cover letter by the 'apply' button below
Education Backgrounds: |
Biomedical Science Healthcare Science |
Specialties: |
(Bio) Chemistry Biomechanics / Tissue Biomedical Engineering Biosystems Pharmaceutics |
Education Level: |
Postgraduate (Masters) |
Experience: |
0 - 2 years 2 - 5 years |
Languages spoken: |
English |
Job Location: | , Belgium |
Type: Job
Deadline: 4th November 2013
Job reference (ID): 6601
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