Job expirat
Assist Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines
Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. Assist with periodic review of study files for accuracy and completeness
Assist CTLs with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information
Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
Requirements
The successful candidates will demonstrate strong administrative skills as well as the ability to multitask, prioritise, show initiative and be proactive. As a team player, you will you will also need to possess effective communication and interpersonal skills. Competence in the Microsoft Office suite is essential, knowledge of Lotus Notes and the pharmaceutical industry would be advantageous.
Awareness of knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines preferred
Knowledge of applicable protocol requirements as provided in company training
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
Strong written and verbal communication skills in local language and good command of English language
Effective time management and organizational skills
Attention to detail and accuracy in work
Ability to establish and maintain effective working relationships with co-workers, managers and clients
School diploma/certificate or educational equivalent
Or equivalent combination of education, training and experience; BS/BA preferred