Linical

About Linical

Job Id. SMW-UK-20191030 Location(s): United Kingdom Company Name: Linical Industry: CRO Job Type: Indefinite Job Duration: Indefinite Salary: Competitive (according to the candidate’s value) Benefits: Competitive (according to the candidate’s value) Linical Co., Ltd. (‘Linical’) is a premier global CRO headquartered in Osaka, Japan, listed in the prime segment of the Tokyo Stock exchange, and dedicated to serve its clients as a true partner in development. With approximately 900 employees Linical directly covers a total of more than 20 countries in Europe, North America and Asia-Pacific including Japan via its own offices and staff. Linical’s European arm is headquartered in Frankfurt, Germany with a substantial presence in Paris and Madrid. Its geographic footprint facilitates a significant presence in the leading Western European markets, combined with well-established affiliate operations in key emerging markets in Central- and Eastern Europe. We offer individualized solutions that are tailored to the specific needs of our sponsors. We work as integrated teams functioning with maximum transparency throughout each study, making sure that the sponsor is kept up to date on all study parameters and progress. We are dedicated to the highest standards of quality, with a special focus on the therapeutic areas oncology, immunology and CNS, based on experience and expertise. Description of the tasks / routine work: Drafting, editing and reviewing according to applicable SOPs (where appropriate), independently and/or in conjunction with other members of the study team and with the client: study protocols and synopses final study reports (including appendices) informed consent forms and Patient Information Sheets peer-review journal articles (clinical and preclinical) conference abstracts and posters (clinical and preclinical) scientific / medical reports (clinical and preclinical) regulatory documents (IBs, IMPDs/INDs, Clinical Summaries and Overviews) Verification of adequacy and completeness of statistical analyses Training of junior medical writers Review of documents prepared by other medical writers Co-ordination of internal study team, including project timeline management, and communication with clients Translations and editing of documents in native language Provision of technical support for Word Filing of medical writing related documents Skills required: Clear and accurate expression in scientific / medical / technical writing and interpretation Structured thought-processes with strong abilities in analysis, logic and interpretation Attention to detail Ability to multi-task and work as part of a team Good communication skills Scientific / medical research experience Sense of professionalism Advanced Word skills Are you ready for the challenging and exciting work within an international team, in a well-established but also fast growing CRO? Are you target-driven, used to sharing your expertise with a team and always focused on the team’s success? We offer a competitive salary and benefit package reflecting your level of experience.

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Company Info

Legal Form: Co

Company Type: Private

Company Size: 501 - 1000

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