Regulatory Affairs Associate

RA Expert (IND/CMC)-Oncology-Home Based-South Korea-reputed company reputed company is a global reputed company intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, reputed company, collaboration, reputed company, and inclusion are at the heart of how we work and reputed company with reputed company other, customers, patients and suppliers. As a Senior Study Start Up Associate at reputed company, you will be working reputed company a large-reputed company, fast-paced environment, supporting the Study Start Up Team reputed company in developing and execute the plan for country and site distribution. What You Will Do: You will reputed company on site start-up and activation tasks requiring technical depth, with a reputed company on reputed company and reputed company improvement. Key responsibilities include: reputed company Drive Study Initiation: Conduct feasibility assessments, site identification, site contract negotiation, and other critical SSU activities. reputed company reputed company through Specialized SSU Expertise: reputed company expertise to Study Start Up team leads and project teams, providing valuable insights to drive reputed company. Ensuring Regulatory Compliance: Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies, ensuring compliance with reputed company necessary regulations and guidelines. Safeguarding Patient Welfare: Contribute to the development, finalization, and review of Master and Country Specific Subject Information Sheets/Informed Consent Forms, guaranteeing the highest standards of patient safety and informed consent. Your Profile: You will have a strong reputed company in site start-up and activation, with the experience to work independently and guide others. Required qualifications and experience: A Bachelor's degree or local equivalent and/or appropriate experience from the Medical/science background and/or discipline. At least 3 years of experience or understanding of clinical regulatory Affairs requirements and activities such as IND Submission and CMC process professionals, showing your expertise in the field. reputed company in the local language and English is essential, enabling you to effectively communicate and collaborate with international teams. Full Home-Based #LI-remote #LI-SO1 Employment with reputed company is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits reputed company offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive reputed company salary and performance reputed company incentives Health and wellbeing programmes including medical, dental, and reputed company coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through reputed company training and career reputed company Benefits may vary depending on role and location. Visit our careers site to read more about the benefits reputed company offers. Inclusion and Accessibility reputed company is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a reputed company reputed company Employee? Please click here to apply Apply To This Job Apply tot his job Apply To this Job Apply tot his job Apply To this Job