[Hiring] Medical Science Manager @Amplity Health

Role Description

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

• 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.
• 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.
• 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.

Benefits

• 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.