Medical Science Manager, Oncology, LATAM

Amplity; Brasil; Presencial; BRL 300 000 - 420 000; Tempo integral

Resumo da oferta

Amplity is seeking an experienced Medical Science Manager to lead clinical trial support in oncology. You will work with investigators and sites to drive enrollment, communicate scientific data, and foster relationships with KOLs and healthcare stakeholders.

In a fast-paced biotech setting, you will collaborate with Medical Affairs and cross-functional teams while ensuring regulatory and ethical compliance. Travel within the territory is expected.

Qualificações

• Minimum 3 years of Medical Science Manager/MSL or equivalent Medical Affairs experience in pharma/biotech.
• Solid tumour oncology experience, with preference for prostate cancer, GU oncology, and/or lung cancer.
• Strong background in clinical development, medical affairs, and healthcare systems.

Responsabilidades

• Clinical Trial Support: engage investigators and study sites, drive enrolment and retention, identify sites and investigators.
• Scientific & Medical Leadership: provide accurate scientific information, develop KOL relationships, support education programs.
• Compliance & Collaboration: partner with Medical Affairs and cross-functional teams, ensure regulatory/ethical compliance.

Conhecimentos

English fluency

Stakeholder engagement

Travel willingness

Formação académica

PharmD/PhD/MD or equivalent degree

Descrição da oferta de emprego

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 Medical Science Manager/MSL, or equivalent Medical Affairs 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.