Medical Science Liaison

GENESIS Pharma; Warszawa; On-site; PLN 180,000 - 240,000; Full time

Job summary

GENESIS Pharma in Central Poland is seeking a Medical Affairs professional to act as scientific resource for HCPs, deliver MIM, and support disease awareness in oncology and rare diseases.

You will conduct advisory boards, support reimbursement with data and presentations, and develop local Medical Plans, attending meetings and reporting insights from congresses.

Qualifications

• University degree in Life Sciences.
• Minimum 5 years of experience in a similar position (Onco / Rare Diseases).
• Fluency in spoken and written English.
• Experience in clinical trials or regulatory/pharmacovigilance roles is a plus.
• Strong interpersonal, organizational, and time management skills.
• Ability to work in a fast-paced, cross-functional environment.
• Excellent proficiency with business and communication tools.

Responsibilities

• Acts as scientific resource for health care providers and handles Medical Information Requests.
• Performs Medical Disease Awareness visits and gathers HCP insights on unmet needs.
• Conducts Advisory Boards with KOLs as needed.
• Supports reimbursement by delivering medical data and presentations.
• Informs stakeholders about data from local HCPs and congresses.
• Develops local Medical Plans aligned with Global Medical Strategy.
• Attends local, regional, and international medical meetings.
• Gathers and reports qualitative and quantitative data from journals.

Skills

Life sciences background

English fluency

Interpersonal skills

Organizational skills

Time management

Problem solving

Business communication

Education

University Degree in Life Sciences

Job description

Established in 1997, by a group of people who recognized early on the power and potential of pharmaceutical biotechnology, GENESIS Pharma was the first pharmaceutical company in Greece and one of the first in Europe to focus on the commercialization of new and innovative biopharmaceutical products. Shortly after its founding, the company began to steadily expand at a regional level, today covering most countries in the CEE region. The robust network of its strategic partnerships comprises leading international pharmaceutical companies dedicated to cutting-edge R&D, alongside fast-growing biopharmaceutical companies with pioneering research and disruptive innovations in the development of targeted, specialized treatments for orphan diseases. In total, GENESIS Pharma holds a product portfolio covering over 30 serious and rare diseases, predominantly within the therapeutic areas of neurology, genetic diseases, oncology, hematology, rheumatology, dermatology, nephrology, gastroenterology, and cardiology.

Do you enjoy interactions with medical experts? Are you interested in working in the field of dermatology and allergology? If so, this role may be for you!

Location: Central Poland

Responsibilities:

• Acts as a scientific resource for health care providers (HCP’s), as required, for unsolicited Medical Information Requests.
• Performs Medical Disease Awareness visits and provides the Organization with important HCP insights to Disease Management and Unmet Medical needs.
• Conducts Advisory Boards with KOLs, depending on the scientific needs.
• Supports Country Lead and Market Access function in reimbursement process by delivering medical data, presentations and answering questions related to the medical nature .
• Informs key stakeholders regarding data generated from local HCPs.
• Establishes and maintains a functional working relationship within the organization, providing scientific support as necessary and/or upon request to other Departments: Medical, Quality, Marketing, Market Access, Legal and Compliance.
• Ensures scientific compliance of activities according to the local applicable laws and SOPs.
• Performs Quality Check on regulatory translations in local language upon Regulatory department request.
• Participates in special projects (at a local and regional level) and Patient Support Programs as required.
• Develops and implements local Medical Plans, in line with Global Medical Strategy.
• Attends assigned medical and scientific meetings (local, regional, and international).
• Develops required qualitative and quantitative reports from abstracts, journals etc.
• Gathers information and gives feedback from local and global congresses.
• Discusses feedback from journals, local and international congresses with the KOLs.

Travel Requirements

• A valid driver’s license is required.
• Ability and willingness to travel, including overnight travel to accomplish field scientific responsibilities.

Qualifications:

• University Degree in Life Sciences.
• Minimum 5 years of experience in a similar position (Onco / Rare Diseases).
• Experience in clinical trials / in Medical Department or Clinical Department/in Regulatory affairs or/and pharmacovigilance roles, is considered a plus.
• Fluency in spoken and written English.
• Strong interpersonal skills.
• Strong organizational and time management skills.
• Solid ability to work in a fast-paced environment.
• Strong problem-solving and decision-making skills.
• Excellent proficiency in business and communication tools.

We offer:

• We offer an attractive remuneration package, continuous training, and career development in an international, fast – paced and dynamic working environment.