Ctry Approval Spec

Work Schedule Standard Office Hours (40/wk) Environmental Conditions Office Job Description At Thermo Fisher Scientific,   you’ll   discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier,   cleaner   and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step   beyond through   research,   development   and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.    Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to   monitoring   through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and execute high-quality, cost-efficient clinical studies.   Discover Impactful Work:   As a Country Approval Specialist, you will support study   startup   by   participating   in the management and preparation,   review   and coordination of country submissions in line with global submission strategy.    A day in the Life:   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:

Bachelor's degree or equivalent and relevant formal academic / vocational qualification    Experience   Previous   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 role   Knowledge, Skills, Abilities   Effective oral and written communication skills   Excellent interpersonal skills   Strong