Medical Director GRITCH

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8b0wyc

pSelect how often (in days) to receive an alert: /p pThe Medical Director has a direct reporting line to the Country Manager. /p pIts main function is to ensure that all scientific and clinical activities comply with current regulations and support the company’s strategic development. /p pThe Medical Director plays a key role in facilitating communication between the scientific and corporate worlds. Medical Director collaborates with research teams, interprets the results of clinical trials and contributes to defining the therapeutic indications for medicines. Furthermore, he or she supervises scientific publications and attends international conferences and meetings, representing the company within the medical and scientific community. /p pThe Medical Director is expected to comply with all Accord Healthcare Processes and any relevant National guidelines*. /p p*The European Federation of Pharmaceutical Industries and Associations (EFPIA) Code of Practice, as well as the EU Directive 2001/83/EC and Members' national codes and local regulations, guide the interactions between the pharmaceutical industry/ Medical Director and HCPs/Patients Association. /p h3The Role /h3 ul liTo lead, organise and manage the medical department to ensure the implementation of the company’s strategy. /li liDevelop and execute the local Medical Plan strategy in alignment with global strategies. /li liManage the planning and execution of medical activities and programs, including investigator-initiated studies, real-world evidence generation, advisory boards, and scientific exchange events /li liResponsibility for the clinical development programs /li licoordinate and facilitate unsolicited Investigator Initiated Trials (IIT) requests, presentation, and publication, in alignment with Medical Affairs’ objectives; /li lisupport the Accord Healthcare/ICTAS Sponsored Studies (Phase I to IV) operations when appropriate; /li liidentify and drive opportunities to generate real‑world‑evidence data.



/li liCompetitive intelligence on clinical aspects on molecules in the market and in development /li liResponsible for the internal cross‑functional collaborations as a scientific partner /li liCollaborate with commercial staff (Marketing, Sales or NPL team) providing scientific expertise and training to commercial staff as required, reviewing and approving promotional materials in accordance with the local SOP and local law; /li liattend the local brand teams; /li lisupport Market Access supporting the PR Dossier finalization, hospital formulary submissions and upon request to present the scientific data on Accord Healthcare products; /li liSupport Regulatory /li liActs as a clinical interface and actively solicits Key Opinion Leader (KOL) interactions related to the molecule and disease area /li liConduct fair and balanced scientific exchanges with KOL to explore mutual clinical and scientific interests, insights generation, scientific/educational meetings (congresses, symposia, etc.), potential research collaborations; /li liidentify opportunities for collaboration with when aligned with Accord Healthcare strategy; /li lidevelop and enhance scientific and educational collaborations with HealthCare Professionals (HCPs) within the Healthcare community and act as a medical contact for KOL and external medical experts. /li liSupport the launch and lifecycle management of Accord’s product portfolio by delivering relevant medical education, data generation, medical insights, and effective collaboration with global teams. /li liReview and approval of promotional and non-promotional materials, ensuring the respect of the medical and regulatory standards. /li liInteraction at Corporate level /li /ul h3The Person /h3 ul liExperience in delivery of scientific presentations and development of relationships with Thought Leaders is strongly preferred, /li liIdeally,



knowledge in data analysis and statistics for purpose of understanding clinical study results, /li liIdeally, current working knowledge of legal, regulatory, and compliance regulations and guidelines relevant to industry interactions with health-care professionals, /li liExpert/fluent communicator in their local language and excellent knowledge of written and spoken scientific English /li liBiomedical, Scientific University education ideally to post-graduate degree level e.g. MSc, PhD, MD, PharmD, /li liMedical/Paramedical Practice or Research career (hospital and/or hospital related, university research, pharmaceutical industry research or medical affairs), /li liPreferably at least 5 years of experience in pharmaceutical industry, /li liIdeally, experience in one or more respective therapeutic areas associated with Accord Healthcare portfolio. /li /ul pOther: /p ul liConvey scientific information briefly, clearly, and precisely, /li liPossesses a scientific qualification with significant scientific and/ or medical/clinical experience, /li liThe ability to understand, process, communicate and present scientific information to a high standard /li liPossess excellent presentation skills, /li liExternal customer focus with strong networking capabilities and integration with Tough Leaders, /li liExcellent influencing, networking, presentation and communication skills and a proven track record of team cross-functional team working, /li liAbility to manage multiple projects and adapt priorities according to business and strategic needs /li liDriving licence. /li liComply with highest ethical standards, with a working knowledge of relevant clinical regulations and industry standards as e.g. GCP, /li liHigh level of emotional intelligence and motivation, /li /ul h3The Rewards /h3 pInternational Enviroment /p pHybrid Model /p pBase salary based on experience and interview outcome: 105.000 - 120.000 EUR gross/year /p pCompany car /p pFlexibility /p pAll applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or disability. /p #J-18808-Ljbffr

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8b0wyc