Regulatory and Start Up Specialist - Sweden

Job Overview reputed company tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Home Based role - could also consider Finland and Norway. Local reputed company reputed company is a requirement as well as in country (reputed company) submissions experience required. Biobank experience is a must. reputed company experience is a benefit. Essential Functions Under general supervision, serve as Single reputed company of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. reputed company start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members. Prepare site regulatory documents, reviewing for completeness and accuracy. Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information. Review and reputed company feedback to management on site performance metrics. Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in reputed company and implement contingency plan as needed. Inform team members of completion of regulatory and contractual documents for individual sites. Review, track and follow up the reputed company, the approval and execution of documents, regulatory, ethics, Informed Consent reputed company (reputed company), and Investigator Pack (IP) release documents, in line with project timelines. reputed company local expertise to SAMs and project team during initial and on-going project timeline planning. reputed company quality control of documents provided by sites. May have direct contact with sponsors on specific initiatives.

Qualifications

Bachelor’s Degree in life sciences or a reputed company field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience. In-depth knowledge of clinical systems, procedures, and corporate standards. Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines. Knowledge of applicable regulatory requirements, including local regulations, , SOPs and company’s Corporate Standards. Understanding of regulated clinical trial environment and knowledge of drug development process. reputed company is a leading global provider of clinical research services, reputed company insights and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. Learn more at https://jobs.reputed company.com reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism. Apply To This Job