Contract Clinical Registries Specialist
Clinical Trial Registries Specialist – CONTRACT – Buckinghamshire – competitive remuneration Our client is a bold, global pharmaceutical company that’s focused on developing, manufacturing and commercialising branded pharmaceuticals, devices and biologic products for patients around the world. The Clinical Trial Registries Specialist’s main responsibilities include: * Providing support to Registry submission activities for clinical trials * Giving guidance and expertise in global registry requirements and data disclosure commitments * Taking responsibility for and leading registry submission process improvement initiatives * Working as a team with other functional areas to ensure compatibility of data across global registries * Ensuring quality assessments of global registry health is carried out for acquired and divested products * Analysing study-related global data disclosure commitments (e.g. ICMJE, PhRMA, EFPIA), and registry requirements (e.g. FDA, EMA, ROW), and taking charge of implementing activities to achieve best practice * Mentoring and supporting junior team members * Conducting your work in compliance with all relevant laws, regulations and regulatory guidelines Applicants will have/be: * Educated to degree level (preferably in life sciences) * Working knowledge and experience within Clinical Trial Registry Management or Clinical Trial Management * Sound regulatory knowledge of regulatory authorities, laws and associations * Strong understanding of Registry requirements * Excellent verbal and written communication skills * Good analytical thinking, observation and problem-solving skills * Excellent computer skills, ideally within clinical trial management systems and electronic document management systems * Ability to multi-task and work well within a team Apply for this Contract Clinical Trial Registries Specialist opportunity now via this website, or call Ashlee on 01628 581 240!Star is a full service resourcing and outsourcing company which resources at all levels for pharmaceutical, medical devices and technology, clinical research and healthcare communications companies in the UK and Ireland on a headcount and outsourced basis. If you haven’t heard from us within 7 working days of submitting your application, please assume that you haven’t been successful on this occasion. We wish you the best of luck with your job search.