Main Responsibilities:
• Responsible for researching, writing, proofing, and editing of complex clinical documents including study protocols, clinical/statistical reports, manuscripts, abstracts and other scientific documents.
• Analyze, interpret, and present extremely complex data from a broad range of scientific disciplines.
• Assure consistency between text and tabular presentations or graphical displays.
• Responsible for journal submission process including preparing and coordinating all documents required for submissions in peer-reviewed journals.
• Work closely with study teams to ensure that documents are scientifically accurate, internally consistent, and meet intended purpose.
• Prepare documents in accordance with internal standards and external regulatory requirements.
Qualifications and Experience:
• Bachelor’s degree or MS/PhD in a relevant scientific discipline (medical-related field).
• Approximately 2 – 4 years of relevant writing experience; ideally combined with experience in clinical research.
• Strong writing skills in authoring and managing the production of scientific documents, including excellent grammatical, editorial, and proofreading skills.
• Previous publications in peer-reviewed journals.
• Fair knowledge of biostatistics is preferred.
• Solid understanding of the drug development process and relevant regulatory guidelines.
• Ability to manage timelines and quality of work using strong communication and interpersonal skills in a cross-functional team.
Please send your CV to jobs@clinart.net mentioning the Job Title in the subject AND Apply Here
• Responsible for researching, writing, proofing, and editing of complex clinical documents including study protocols, clinical/statistical reports, manuscripts, abstracts and other scientific documents.
• Analyze, interpret, and present extremely complex data from a broad range of scientific disciplines.
• Assure consistency between text and tabular presentations or graphical displays.
• Responsible for journal submission process including preparing and coordinating all documents required for submissions in peer-reviewed journals.
• Work closely with study teams to ensure that documents are scientifically accurate, internally consistent, and meet intended purpose.
• Prepare documents in accordance with internal standards and external regulatory requirements.
Qualifications and Experience:
• Bachelor’s degree or MS/PhD in a relevant scientific discipline (medical-related field).
• Approximately 2 – 4 years of relevant writing experience; ideally combined with experience in clinical research.
• Strong writing skills in authoring and managing the production of scientific documents, including excellent grammatical, editorial, and proofreading skills.
• Previous publications in peer-reviewed journals.
• Fair knowledge of biostatistics is preferred.
• Solid understanding of the drug development process and relevant regulatory guidelines.
• Ability to manage timelines and quality of work using strong communication and interpersonal skills in a cross-functional team.
Please send your CV to jobs@clinart.net mentioning the Job Title in the subject AND Apply Here
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