Medical Writer Jobs in Genf
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Suchergebnisse - Medical Writer Jobs in Genf
CTC Resourcing Solutions-Genf
the latest in skill development training programmes.
Medical Writer
Our client, a global provider of blood and plasma supplies and services, is looking for a Medical Writer. This is a permanent rolebased in Vaud, Switzerland(can be anywhere in Switzerland...
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World Health Organization-Genf
experience in a regional/international public health institution on STI surveillance and STIs programmes in an LMIC (Low and Middle-Income Countries).
Skills
Excellent research, writing and communication skills.
Resource mobilization, external relations...
France Life Imaging-Genf
Type de structure : Bracco Suisse SA is a company of the international Bracco Group ( a leader in contrast agents for medical imaging. R&D is articulated between 2 Group’s centers, in Colleretto Giacosa- Italy, next to Ivrea (CRB – Bracco Research...
Cagi-Genf
Ability to analyse medical data.
• Ability to provide technical paediatric support to projects in low resource settings.
• Excellent writing skills.
Languages
• Fluency in English is required.
• A good working knowledge of French is expected.
Personal...
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HELVETICA PARTNERS-Genf
all software release activities (e.g., testing of software, writing of application notes & manuals & training sessions).
2. Provide technical support for global users.
3. Collect feedback from users & partners & collaborate with research & development...
France Life Imaging-Genf
Type de structure : Bracco Suisse SA is a company of the international Bracco Group (www.bracco.com), a leader in contrast agents for medical imaging. R&D is articulated between 2 Group’s centers, in Colleretto Giacosa- Italy, next to Ivrea (CRB...
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CyberPeace Institute-Genf
Institute is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, marital status, medical condition, national...
Mikajaki-Genf
nodes, sensors, and actuators. It must meet the functional requirements defined by the stakeholders, and the safety and reliability requirements defined by medical standards.
MIKAJAKI is located in Plan Les Ouates (Geneva).
Responsibilities:
1. Lead...
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Teoxane-Genf
experience in the Pharmaceutical or Medical Device industry
• Good experience in commissioning and system qualification
• Pedagogue, communication skills and good writing skills
• Strong organizational, communication, and interpersonal skills
• Dynamic...
Mölnlycke Health Care AG-Genf
and project schedules.
English written and spoken fluently.
Strong technical writing and reporting skills.
A recognized academic qualification in microbiology, pharmacy, quality, or chemistry.
At least five years of working experience within the quality area...
Teoxane SA-Genf
regulations, and internal SOPs in clinical projects, - Able to work cross functionally within Teoxane departments to prepare required study documentations for submission to Ethic Committees and competent authorities which includes oversight, writing and review...
International Organization for Migration-Genf
of relevant professional experience.
Experience:
Experience with executive support in headquarters and field locations.
Experience in liaising with government and diplomatic authorities and international institutions.
Experience in writing executive...
Teoxane SA-Genf
to prepare required study documentations for submission to Ethic Committees and competent authorities which includes oversight, writing and review of documents, - Develop and manage the overall clinical study budget, - Select and validate investigator/site...
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Teoxane SA-Genf
Any other specific assignment that may be entrusted to you by the Management
Your profile
• Minimum 7 to 10 years of experience in Medical device industry
• Proficient knowledge of quality standard (ISO 13485) and relevant regulations (21CFR part 820...
World Health Organization-Genf
systematic reviews of the literature in the field, input to evidence-based clinical and managerial guidelines.
6. Ensure the writing and preparation of technical progress reports to governing and advisory bodies, WHO reporting requirements, and donors.
7. ..
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