Study Physician (m/f/d) - Inflammation

Boehringer Ingelheim GmbH; Wien; Vor Ort; EUR 108.000 - 132.000; Vollzeit

Benefits dieser Stelle

Flexible working time

Bridge-days

Canteen & Cafeteria

Learning & development

Public transport support

Health promotion

Zusammenfassung

Boehringer Ingelheim Austria is seeking a Study Physician (MD) to provide end-to-end medical support across the study lifecycle, from Trial Design Outline to Clinical Trial Report, collaborating closely with Clinical Trial Leaders and safety teams.

The role requires medical expertise in inflammation, a minimum of four years of active clinical practice, and openness to flexible working time models as part of comprehensive employee benefits.

Qualifikationen

• Physician (MD) trained in a clinical setting, with four years of active clinical practice.
• Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, or Emergency Medicine is desirable.

Aufgaben

• Provide end-to-end medical support throughout the study lifecycle, from trial design to Clinical Trial Report.
• Ensure high-quality medical content of trial documents, collaborating with CTL, CPL, Patient Safety Physician, and cross-functional teams.
• Contribute to medical risk management and development of CQMP, including monitoring protocol deviations.
• Lead medical training for investigators and study teams; contribute to eCRF design, data checks, ICF, lab alerts, recruitment and retention activities.

Ausbildung

MD (Physician) degree

Jobbeschreibung

Study Physician (SP) is a critical role within Clinical Development Inflammation to establish readily available medical support and consultancy for clinical trials within Inflammation Therapeutic Area by a qualified and clinically experienced physician. Medical input for the clinical trial and being involved in the project/asset team by provision of state-of-the‑art medical expertise with the aim to execute medical oversight and support in management of clinical trials during the preparation, conduct, and reporting phase of clinical trials. Study Physician is a core member of the Trial Team and member of the Evidence Network for the asset.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides an opportunity for all employees to collaborate internationally, offering visibility and the opportunity to directly contribute to the company's success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work‑life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

This position can be filled in different countries.

Tasks & responsibilities

• Responsible for end‑to‑end medical support throughout the entire study lifecycle, from Trial Design Outline kick‑off to the Clinical Trial Report
• Ensures high‑quality medical content of the Clinical Trial Protocol and contributes to other core trial documents, by collaborating closely with Clinical Trial Leader (CTL), Clinical Program Lead (CPL), Patient Safety Physician, and other cross‑functional stakeholders.
• Strong contribution to trial risk‑based quality management from medical perspective, by defining medically relevant critical data/processes, related risks, and its mitigation/monitoring strategies. Takes medical responsibility for agile & adaptive medical data review including development of the Clinical Quality Monitoring Plan (CQMP) and defines important protocol deviations.
• Responsible for medical training for investigators and study team. Contributes to eCRF design, automated data checks, ICF, lab alerts, recruitment and retention activities, regulatory and ethics responses.
• Responsible to answer medical questions from Investigators, and contributes to adjudication and Data Monitoring Committee processes.

Requirements

• Physician (MD) (ideally with medical thesis), trained in a clinical setting, and minimum of four (4) years of active clinical practice experience; specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, and Emergency Medicine is desirable.
• Experience specifically in Inflammation Clinical Development is preferred. Experience in pharma industry or CRO in medical or project management functions (ideally in Clinical Development) is desirable.
• Ability to communicate directly and concisely while collaborating with key stakeholders, pronounced presentation and training skills. Capability to work proactively and with team spirit in an international environment and team.
• Pronounced analytical skills and systematic and well‑structured working style.
• Displays the ability to use digital technologies to access information, be creative, innovative, solve problems, communicate, navigate, learn & apply in a digital environment.
• Flexible working time models: home office and flexible working hours, depending on department and position - many things are possible with us.
• Additional days off ("bridge-days"): more free time through additional days off to bridge single working days between bank holidays and the weekend - without having to use vacation days.
• Canteen & Cafeteria: whether it's coffee and croissant for breakfast, various lunch menus or snacks in between - our subsidized staff restaurant & cafeteria has something for every taste including vegetarian and vegan options.
• Learning & development: diverse training and development opportunities for your personal and professional growth. Because: you never stop learning.
• Health promotion: health is important to us - that's why we offer different programs to promote physical and mental health.
• Public transport ticket: we encourage our employees to use public transport on their daily way to work. Costs for public transport? We cover them!

The remuneration for this position starts at EUR 120.300 gross annual target salary per year (full time). The actual salary package depends on professional experience and qualifications. We will be happy to discuss further details in person.