Work Schedule

Standard Office Hours (40/wk)

Environmental Conditions

Office

Job Description

Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy.Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients.Provides project specific local Startup services and coordination of these projects.May have contact with investigators for submission related activities.Key-contact at country level for either Ethical or Regulatory submission-related activities.Coordinates, under guidance, with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation.Achieves company’s target cycle times for site.May develop country specific Patient Information Sheet/Informed Consent form documents.May assist with grant budgets(s) and payment schedules negotiations with sites.Supports the coordination of feasibility activities, as required, in accordance with agreed timelines.Enters and maintains trial status information relating to Startup activities onto company tracking databases in an accurate and timely manner.Ensures the local country study files and filing processes are prepared, set up and maintained as per company WPDs or applicable client SOPs.Maintains knowledge of and understand company SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided.Keys to Success:EducationBachelor's degree or equivalent and relevant formal academic / vocational qualificationExperiencePrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years)In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the roleKnowledge, Skills, AbilitiesEffective oral and written communication skillsExcellent interpersonal skillsStrong attention to detail and quality of documentationGood negotiation skillsGood computer skills and the ability to learn appropriate softwareGood English language and grammar skillsBasic medical/therapeutic area and medical terminology knowledgeAbility to work in a team environment or independently, under direction, as requiredBasic organizational and planning skillsBasic knowledge of all applicable regional / national country regulatory guidelines and EC regulations