Back to positions

Regulatory Affairs Associate

Remote role Full-time Open position

RA Expert (IND/CMC)-Oncology-Home Based-South Korea-ICON Strategic Solutions ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. As a Senior Study Start Up Associate at ICON, you will be working within a large-scale, fast-paced environment, supporting the Study Start Up Team Lead in developing and execute the plan for country and site distribution. What You Will Do: You will lead on site start-up and activation tasks requiring technical depth, with a focus on quality and continuous improvement. Key responsibilities include: Efficiently Drive Study Initiation: Conduct feasibility assessments, site identification, site contract negotiation, and other critical SSU activities. Empower Success through Specialized SSU Expertise: Provide expertise to Study Start Up team leads and project teams, providing valuable insights to drive success. Ensuring Regulatory Compliance: Prepare and coordinate submissions to regulatory, ethics, and other relevant bodies, ensuring compliance with all 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 foundation 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. Fluency 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 ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON 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 current ICON 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

Further positions

Want (Remote) Principal Regulatory Affairs Specialist, Software in USA

Remote role Full-time

Associate Regulatory Affairs Specialist (Acute Care and Monitoring)

Remote role Full-time

Hiring Regulatory Affairs Associate II (Hybrid Remote)

Remote role Full-time

[Remote] Senior Regulatory Affairs Associate - Labeling Compliance Analytics

Remote role Full-time

Medical Device Regulatory Affairs Specialist

Remote role Full-time

CLINICAL DEVELOPMENT & REGULATORY AFFAIRS ASSOCIATE (ENTRY LEVEL)

Remote role Full-time

Manager/Associate Director, US Regulatory Affairs

Remote role Full-time

Want Associate Director, Global Regulatory Affairs (Remote) in USA

Remote role Full-time

Regulatory Affairs Associate - Hardware

Remote role Full-time

Regulatory Affairs Associate (CMC Lifecycle)- Temporary for 3 years

Remote role Full-time

[Remote] Regional Clinical Manager - WEST

Remote role Full-time

Regulatory Compliance & Risk Management Expert

Remote role Full-time

Experienced Remote Data Entry Research Panelist – Work From Home Opportunity at arenaflex

Remote role Full-time

Medical Director – Dermatologist

Remote role Full-time

Dynamic Remote Customer Service Representative – Technical Support & Client Success at arenaflex

Remote role Full-time

Enrollment Coordinator

Remote role Full-time

Part-Time Online Adjunct Professor- Criminal Justice

Remote role Full-time

Senior MACSS/Mainframe Developer

Remote role Full-time

[Remote] Marketing Specialist

Remote role Full-time

Lead Software Engineer, Fullstack

Remote role Full-time