Medical Science Liaison (Oncology Supportive Care & Biosimilars)

The Opportunity

At Juniper Biologics (a holding company Cypress Pharmaceuticals), we don't just hire MSLs to deliver slides, but we hire future medical leaders. This role offers a unique balance: you will drive the medical strategy for our core established portfolios while gaining exposure to Business Development and New Product Planning.

We are looking for a scientifically robust professional, who understands the nuances of hospital formularies and is ready to expand their skill set into launch management and pipeline evaluation. This role also encompasses oversight of PV and QA activities across SEA, AU and MEA

Key Responsibilities

1. Core Portfolio Management

Supportive Oncology

o Drive scientific engagement on Chemotherapy-Induced Nausea and Vomiting (CINV) pathways.

o Work with Oncologists and Pharmacists to entrench CINV protocols in SEA/MEA hospitals.

Biosimilars (Singapore only)

o Act as the technical authority on biosimilarity, safety and efficacy data.

o Address questions regarding interchangeability and switching studies to support hospital formulary listings.

2. Regional Medical Support (Remote MEA & SEA)

Dedicate approximately 50% of your time to supporting the Medical Director with the MEA and wider SEA markets.

Note: This function is fully remote. You will provide literature reviews, medical query responses and slide deck localisation for partners in these regions without the need for international travel.

3. Pharmacovigilance (PV) & Quality Assurance (QA) Lead

Pharmacovigilance

o Safety Case Management & Compliance: Manage timely, compliant safety reporting (ICSRs,

PSURs, RMPs), literature screening and data reconciliation across all markets.

o Safety Surveillance & Quality Oversight: Support signal detection, monitor safety trends, and maintain PV system readiness, including leading audits/inspections and CAPA management.

o PV Governance & CrossFunctional Coordination: Ensure alignment with SOPs and regulatory requirements, and coordinate accurate, timely medical information responses with the MSL team.

Quality Assurance

o Quality Operations & Compliance: Oversee product complaints, batch release documentation, and quality issue management (excursions, deviations, investigations, recalls, and product disposition).

o Vendor & Partner Quality Oversight: Lead PV/Quality Agreement development, conduct vendor due diligence, and maintain ongoing oversight of partner performance and GDP compliance.

o Quality Systems, SOPs & Continuous Improvement: Develop and maintain PV/QA SOPs, deliver compliance training, and drive continuous improvement of quality processes and tracking systems.

4. Pipeline & Launch Readiness (New Products)

Act as the medical lead for newly in-licensed assets.

Prepare Day 0 medical frameworks, including identifying Key Opinion Leaders (KOLs), mapping the treatment landscape and adapting global medical & health economics dossiers under the guidance of the Medical Director.

5. Career Development (Business Development)

This is a growth component designed to prepare you for mid-career management.

Partner with the Commercial and Business Development teams to assess the scientific viability of potential new assets.

Assist in drafting medical strategy frameworks for market entry

Requirements

Education

Preferred: Registered Pharmacist

o Why We value your understanding of pharmacokinetics, hospital formulary mechanics and drug interchangeability.

o Considered: Advanced degrees in Life Sciences (PhD, MSc) with relevant experience.

Experience

o 23 years of experience in Medical Affairs, Clinical Pharmacy or a technical commercial role within the healthcare industry.

o Proven ability to interpret complex clinical data (e.g. non-inferiority trials for biosimilars).

Skills & Competencies

o Agility: Ability to balance a portfolio split effectively.

o Communication: capable of having a peer-to-peer conversation with external and internal stakeholders.

o Commercial/Strategic Mindset: An interest in understanding the business of science and how medical evidence supports successful product launches.