Study Physician (m/f/d) - CardioRenalMetabolism TA

The position

Study Physician (SP) is a critical role within Clinical Development CardioRenalMetabolism (CRM) to establish readily available medical support and consultancy for clinical trials within CRM 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.

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 Internal Medicine, Family Medicine, Cardiology, Nephrology, Pediatrics, or Emergency Medicine is desirable.
• Experience specifically in CRM 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.

Your Benefits

• 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.

We are looking forward to receiving your application online!

By uploading your application documents via our application portal, we can treat your data confidentially and in compliance with the GDPR.

Do you have any additional questions about the position? Your HR Recruiting Manager for this position is Marlies Taeufinger.

On our career site you will find further information about Boehringer Ingelheim as an employer as well as information about the application process and our different departments.

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