Country Approval Specialist

• Prepare, review and coordinate local regulatory submissions in alignment with global submission strategy
• Provide local regulatory strategy advice to internal clients under guidance
• Provide and coordinate project-specific local SIA services
• Contact investigators for submission-related activities as needed
• Serve as country-level key contact for ethical or regulatory submission activities
• Coordinate with internal functional departments on site start-up activities and timelines
• Ensure submission processes align with the critical path for site activation
• Achieve PPD target cycle times for sites
• Work with start-up CRAs on regulatory compliance review packages as applicable
• Develop country-specific Patient Information Sheets/Informed Consent Forms as needed
• Assist with grant budgets and payment schedule negotiations with sites
• Support feasibility activities according to agreed timelines
• Enter and maintain trial status information in PPD tracking databases
• Prepare, establish and maintain local country study files and filing processes
• Maintain knowledge of PPD SOPs, client SOPs/directives and current regulatory guidelines

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• Previous experience comparable to 2+ years
• Effective oral and written communication skills
• Excellent interpersonal skills
• Strong attention to detail and quality of documentation
• Good negotiation skills
• Good computer skills and ability to learn appropriate software
• Good English language and grammar skills
• Basic medical/therapeutic area and medical terminology knowledge
• Ability to work in a team environment or independently, under direction, as required
• Basic organizational and planning skills
• Basic knowledge of applicable regional/national country regulatory guidelines and EC regulations
• In some cases, an equivalency combining appropriate education, training and/or directly related experience may meet requirements