Specialist, Regulatory & Site Activation - South Korea- Remote

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Join us!

Our Regulatory Affairs team boastspractical knowledge in the North American and International regulatory arenas through all phases of the drug‑development process. Weholdextensive industry experience shaping project plans to meet diverse regulatory requirements.

Our expertsstrategize the most efficient route for our clients’products, from bioanalytical study requirements, pre-IND/pre-NDA meetings with the FDA, and applications to Competent Authorities and Ethics Committees, to successful marketing applications, whileprovidingthe necessary guidance to ensure continual regulatory compliance.

• Liaise with SAR colleagues to drive plan, organize, compile, progress, track, and submit regulatory submissions on a timely basis and with a consistently high level of quality.
• May act as a contact point for translation review of submission documents such as applications, synopses, ICFs, labels, etc.
• Maintain country‑specific patient information sheet and consent form customization text, Maintain country‑specific drug labeling information and Country Intelligence Pages
• Review and make recommendations on all relevant documentation e.g. labels, patient information sheets, diary cards etc. to comply with ICH GCP & country‑specific requirements.

• Organizational and time management skills
• Aptitude for planning, strategizing, managing, monitoring, scheduling, and critiquing skills
• Strong written and verbal communication skills to clearly and concisely present information in English and local language both
• Strong ability to handle multiple tasks in a fast‑paced and changing environment
• Proficiency in MS Office applications, including Microsoft Word, Excel, and Power Point
• Strong understanding of country‑level cultural norms and local healthcare systems; ability to initiate and develop relationships with local investigators and key site personnel.

• A minimum four‑year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or other related sciences
• Minimum three years of experience in clinical research, preferably in site activation and/or regulatory‑related function
• Previous experience within the pharmaceutical/CRO industry.
• Thorough knowledge of ICH GCP, EU Clinical Trials Directive, and other relevant guidance on conducting clinical research.
• Experience in regulatory submissions in South Korea is mandatory
• Multilingualism preferred; working knowledge of English.

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