Medical Science Liaison-Oncology

On behalf of our Client, an international biotech company focused on the development of innovative oncology therapies, IQVIA, a global leader in services for the pharmaceutical and biotechnology industries, is seeking a Medical Science Liaison, Oncology.

The Medical Science Liaison facilitates and develops the relationship with the medical/scientific community including physicians and medical centers, by communicating scientific and medical therapy area related information to investigators and institutions. They provide information on research developments, and new concepts in medical treatment.

The Medical Science Liaison will also participate in close partnership with Site Management & Monitoring staff in the initiation, oversight, and follow-up of clinical studies. This is done in a strictly scientific, non-promotional manner, and in full compliance with applicable laws and regulations, guidelines, codes of conduct.

RESPONSIBILITIES•Provide field-based medical support to Company’s clinical research programs;•Deliver credible presentations on scientific matters in the disease area of responsibility and about company pipeline to investigators in company-sponsored interventional research;•Engage with clinical trial site investigators and staff to understand enrollment/screening barriers from a medical perspective and work with the site and client to find potential medical solutions.

); while ensuring a high level of scientific or educational integrity in these collaborative efforts;•Facilitate medical and scientific field intelligence including maintaining a list of investigators/potential investigators within a given therapy area, understand competitor research activities in active or planned study sites, generate insights from investigators on challenges and opportunities;•Attend relevant scientific meetings and conferences and may represent company in scientific booths at congresses;•Upon request, assist physicians with requests for access to company medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory

requirements;•Ensure that all activities and interactions are conducted with due regard to all applicable local, global, and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice;•Identify, and categorize key opinion leaders (KOL) with an interest in the designated therapy area;•Work with identified stakeholders to establish and enhance the reputation of the company as required and demonstrate themselves to be a partner of choice for consultant clinicians interested in the designated therapy area;•Coach and develop scientific speakers who are actively interested in the designated therapy area through one-on-one clinical training on approved clinical slide sets.

•Territory management, project management and CRM mastery and timely data input;•Reactively and balanced information exchange with thought leaders and insights gathering on new treatment options in development to better serve patient needs and in compliance with applicable laws, rules, and regulations;•Comply with all legal

requirements of the role, all IQVIA compliance

requirements as well as the respective

requirements of the customers are met. Reports of drug risks are sent in writing directly to the defined addressee. All assigned IQVIA mandatory e-learning courses are completed within the defined time frame;•To be an ambassador of IQVIA with the client company at all times.

, client company and published data;•Ability to establish and maintain effective working relationships with coworkers, managers, and clients;•Ability to communicate in both English and native/local language;•Valid driving license required. 000€ RAL. The salary range is defined based on experience, skills, and internal equity criteria. Career progression and compensation review are based on transparent, objective criteria.

We are committed to fair and equal pay practices, in line with applicable pay transparency regulations (EUDirective 2023/970). IQVIA reserves the right to evaluate candidates with domicile / residence and work experience / study with

requirements responding to the open request. Applications WITHOUT the

requirements Will NOT be fully taken into account. Please enter the authorization for the processing of personal data (DL196/2003) - General Data Protection Regulation (13 GDPR 679/16 –) to IQVIA and to transfer those data to IQVIA’s Clients. The research is urgent and is intended for candidates of both sexes (L.903/77). Compensation: 0.000000 - 0.000000.