The posting
Medical Science Liaison (12 months contract)
About the Company: Our client is a Swiss pharmaceutical based corporation that provides solutions to address the evolving needs of patients worldwide. Their main discoveries are development, manufacture and marketing of prescription and generic pharmaceutical products and eye care products.
Primary Responsibilities: In this role you will lead scientific engagement with their Medical Experts. Implement clinical and educational strategies and respond to unsolicited medical enquiries. Implementation and execution of medical affairs plan for assigned therapy area. This role is also responsible for supporting medical governance & operation processes within the department.
The responsibilities includes:
- Engage with Medical Experts (MEs) to educate on medical/scientific information using approved materials per applicable standards
- Ensure appropriate identification/mapping of MEs/ Key Accounts including identification of opportunities to involve MEs when a specific medical need is identified to provide support
- Develop and execute ME engagement plans to effectively prioritize and strategically engage MEs aligned with country strategy.
- Respond to unsolicited requests for information from MEs in a high quality, timely manner, and in accordance with applicable standards
- Inform and shape medical strategy by collecting impactful insights from MEs
- Support the client organization clinical research programs, optimize trial execution and provide scientific educational support to potential and actual study sites in collaboration with clinical operations.
- Facilitate Investigator Initiated Trial (IIT) process upon investigator request
- Serve as a medical resource to field matrix colleagues
- Review & approval of non-promotional and promotional materials developed for local stakeholders
- Reporting of technical complaints/ adverse events/ special case scenarios related to the client’s products within 24 hours of receipt
- Medical information inbox monitoring & monthly pharmacovigilance (PV) reconciliation
- Managed access program and post-study drug supply request monitoring, processing requests & coordination of supply
- Risk management plan (RMP) coordination
Requirements:
- Bachelor’s degree in health-related science / life science / Pharmacy degree with MD / PhD / PharmD qualifications
- At least 2 years of pharmaceutical medical affairs experience
- At least 2 years of Oncology experience
Reg No: R22104540 EA License no: 94C3609



