Lead operator állások, munkák egészségügy, gyógyszeripar területen

• Literature reviews as requested by client epidemiologists using the best practice methodologies
• Literature search and preparation of Literature review report for Pharmacoepidemiology
• Perform peer Scientific & Technical Review

• Perform all tasks and behave in a manner that complies with and supports all safety and stewardship-related company policies and practices, including completing all required company training courses.
• Lead complex projects and deliver on key targets across sites.

• Location: Budapest, Hungary – 9th District, Mill Park office building
• Job Type: Full-time
• Contract: Maternity cover (until the incumbent returns)
• Office Presence: Required once per week

• 40 hours per week
• Normal business hours
• Office attendance: Once a week
• Tracking different regulatory submissions in the corporate regulatory database – update database with specific documents and/or information
• Running daily queries, providing reports to client stakeholders

• Present, promote and inform healthcare professionals about the benefits and features of bredent products.
• Actively sell dental implants and related products distributed by bredent.
• Promote and sell professional trainings, educational services and technical support to both new and existing partners.

Lead the implementation of quality systems and processes for the new facility, ensuring compliance with ​IATF 16949 and ​customer-specific standards (e.g., VDA 6.3, Formel Q, BMW QM-Requirements)....

• Organizational and administrative management of Kecskemét plasma center in cooperation with the Lead Physician and the Quality Management Representative
• Defining and implementing an expedient center strategy
• Leading a team of nurses and physicians – support, develop, motivate, provide regular training

• Receipt / Download / Accepting of cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

• Act as the clinical leader and primary clinical representative for global programs, ensuring high quality and speed of functional deliverables.
• Develop a clinical vision for addressing unmet medical needs, considering the molecule's scientific hypothesis.

• Lead the Near Patient Program in Germany, ensuring high-quality, patient-centred, and compliant care delivery
• Act as the senior clinical voice supporting operational and strategic healthcare decisions

• Lead the Near Patient Program in Germany, ensuring high-quality, patient-centred, and compliant care delivery
• Act as the senior clinical voice supporting operational and strategic healthcare decisions

• Lead the Near Patient Program in Germany, ensuring high-quality, patient-centred, and compliant care delivery
• Act as the senior clinical voice supporting operational and strategic healthcare decisions

• Provide medical leadership for the Near Patient Program in Germany, ensuring effective, compassionate, and compliant service delivery.
• Serve as the primary liaison between local Near Patient staff, military medical providers, and host-nation healthcare facilities.

Lead and coordinate the Site-Launch activities and associated teams for internal and external sites and development projects...

Maintain a database of global medical scientific publications to ensure company-wide awareness of publications related to STAAR surgical products, and to ensure cross-functional access to contemporary and historical publications....

Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the provider....

Provide comprehensive In-patient clinical case management for a patient where they will be completing status reports upon admission and whilst the patient remains admitted to the provider....

• Design and execute experiments for purification of recombinant proteins
• Analyze and interpret data to guide process development and troubleshooting
• Collaborate cross-functionally with other RnD teams
• Contribute scientifically to the project progress, lead project discussions and development

• Active contribution to Product care and a Key role in Product development as the technical lead for the Orbit & Consumables portfolio
• Technical support of product development project team

You will be responsible for supporting the core and senior scientific leadership team by developing, maintaining, and executing programs and strategies across the business....