Purpose

• You will be the main CSL medical contact for both internal and external partners in all interactions and communications requiring medical knowledge and medical expertise on CSL products and relevant therapeutic areas.
• You will contribute to the medical support of the scientific, educational and promotional activities organized by CSL Behring in Türkiye in adherence with CSL values and Code of Responsible Business Practice, regional CSL processes, relevant local and international codes and regulations.
• You will ensure internal training and continuous medical support for the sales and marketing organization and for the medical clearance of promotional and educational materials, as per regional, national and CSL global procedures and guidelines.
• You will maintain the local database and documentation associated with Investigator Initiated trials and / or other clinical activities locally initiated, preparing the clinical documents, and acting as medical contact in relation with CROs and other parties involved in the clinical studies.

• You will participate in the preparation of scientific, promotional and educational events in the region and provides medical expertise needed for preparing these events. Acts as CSL main presenter during internal trainings of Sales and Marketing organisation within the region or external events organised by CSL Behring with participation of health care providers. Is involved in establishing and maintaining business relationship with regional and national KOLs, with key HC administrative bodies, public health organizations, patients' organizations and deals with all medical aspects of these interactions.

• Is responsible for overall medical management of the clinical trials including handling of medical enquiries, investigator selection, protocol, CRF and documents to obtain informed consent, investigator management, adverse event monitoring and report writing and adherence of these trials to main industry and CSL requirements and guidelines.
• You are responsible for medical review of promotional materials.
• You ensure medical input and support in selection of scientific in line with medical evidence and regulatory requirements.

• You are responsible for preparing and updating employee training programs focused on medical aspect of CSL Products.
• You are responsible for distributing medical updates within the region.

• You are responsible for: creating and updating of regional database for medical queries and all related documents.
• You ensure preparation and implementation of regional medical information procedures and adherence to CSL values and Code of Responsible Business Practice

• You perform literature search, prepare literature reviews for internal distribution at regional level and ensure regional dissemination of information received from Commercial Development on relevant literature for CSL Behring products, competitors and/or therapeutic areas.

• You maintain an active interface with internal customers (marketing, market access, sales, regulatory, pharmacovigilance, customer service, other medical colleagues, etc)
• You collaborate with marketing in identifying the relevant KOLs in the relevant therapeutic areas and maintains a speaker and regional KOLs database.

• You ensure and document periodical training and certification of the product knowledge of the Sales Force; ensures continuous medical support and communication with the field force.

• You provide feedback (if requested) on the national treatment approaches in different therapeutic areas; evaluates the medical market for new therapeutic indications.

• You serve as an expert for the regional and marketing organization on matters of compliance with all applicable codes of conduct and affiliate SOPs.

• You ensure that a local business continuity plan exists so that ICSR handling can continue during a crisis.

• You provide a local interface between global organization and local functions such as Commercial Operations / Medical Affairs (incl. medical information) / Commercial Development / Marketing, ensuring all product safety information incl. medical information enquiries received locally are screened and monitored for ICSRs/safety relevant information and handled in accordance with GCSP procedures.

• You provide a local interface between global GCSP organization and all local functions such as local Regulatory Affairs, and the Country/Regional/General Manager to ensure timely implementation of Risk Minimization Measures in the territory.

• Degree in Medicine (MD) or Pharmacy, PhD is a plus.
• English - fluent, Turkish - native
• A minimum of 4-6 years of experience as medical advisor/medical manager
• A minimum of 2-3-year experience as position of Medical Director/Medical Group leader is a plus
• Experience in Biotech, Plasma Products or Rare Diseases area is an asset.