Business Unit: Medical Affairs
Reports to: Program Director, Amplity
Location: Home-based, South Korea
Territory: APAC, up to 50-70% travel
Individual Contributor or Manager: Individual

Purpose of Role

Join an innovative biotech organization at a pivotal stage of growth as it launches its first global Phase III oncology study in prostate cancer, while advancing a broader pipeline in solid tumours, including NSCLC. This highly visible role offers the opportunity to work closely with investigators, key opinion leaders, and study sites, helping drive the success of a landmark clinical program and improve outcomes for patients with cancer.

Key Responsibilities

Clinical Trial Support

• Support company-sponsored clinical studies by engaging investigators and study sites.

• Drive study awareness and support patient enrolment and retention initiatives.

• Identify and recommend potential study sites and investigators.

• Foster strong partnerships with investigators and site staff to ensure protocol adherence and high-quality study execution.

• Serve as a key scientific liaison between study sites and internal stakeholders.

Scientific & Medical Leadership

• Provide accurate, balanced scientific and clinical information within oncology.

• Develop relationships with KOLs, investigators, and healthcare stakeholders.

• Support medical education programs, advisory boards, and scientific exchange activities.

• Represent the organization at congresses, symposia, and external scientific meetings.

• Monitor emerging clinical data, competitive intelligence, and healthcare trends to provide strategic insights.

Compliance & Collaboration

• Partner with Medical Affairs, Clinical Development, and cross-functional teams.

• Ensure all activities are conducted in accordance with regulatory, legal, and ethical requirements.

Qualifications

• PharmD, PhD, MD, or equivalent advanced scientific/clinical degree.

• Minimum 3 years of MSL, or equivalent Medical Affairs or Clinical Operations experience within pharma or biotech.

• Solid tumour experience required, with preference for prostate cancer, GU oncology, and/or lung cancer expertise.

• Strong understanding of clinical development, medical affairs, and healthcare systems.

• Experience working with clinical trials and external experts.

• Excellent communication, presentation, and stakeholder engagement skills.

• Proven ability to work effectively in a fast-paced, cross-functional environment.

• Fluent in English and the local language as required.

• Willingness to travel within the assigned territory.

Why Join?

• Support a company's first global Phase III oncology program.

• Work directly with leading investigators and oncology experts.

• Enjoy significant visibility, autonomy, and impact.

• Contribute to a growing oncology pipeline with strong future development opportunities.