Biometrics and Clinical Research • Contract Research Organisation • biostatistics • data-management • E-CRF
1001 - 5000
November 3
Biometrics and Clinical Research • Contract Research Organisation • biostatistics • data-management • E-CRF
1001 - 5000
• Perform medical writing tasks according to Aixial or sponsor SOPs as applicable • Overall responsibility for co-ordinating and managing medical writing tasks • Prepare documents such as clinical study reports, Investigator’s Brochure (IB) updates, protocols • Prepare scientific publications (conference abstracts, posters, and manuscripts) • Maintain and develop skills within medical writing • Write and review SOPs and procedures within Medical Writing • Training and mentoring of new medical writers
• Ability to structure and plan own work according to agreed timelines • Ability to manage own time • Excellent attention to detail combined with an understanding of the document’s overall purpose • Ability to work simultaneously on more than one project • Ability to establish and maintain effective working relationships with co-workers, managers and clients • Knowledge of GCP as well as relevant ICH guidelines
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