Study Physician

Boehringer Ingelheim Pharma GmbH & Co. KG; Ingelheim am Rhein; Vor Ort; EUR 110.000 - 170.000; Vollzeit

Benefits dieser Stelle

Comprehensive benefits

Wellbeing program

Zusammenfassung

Boehringer Ingelheim Pharma GmbH & Co. KG in Ingelheim am Rhein seeks a Study Physician to provide high‑quality medical support for global clinical trials and contribute to trial planning and conduct.

As an MD with clinical experience, you will collaborate with CTL, CPL, Patient Safety, Medical Writing and trial teams to ensure scientific quality and timely delivery of core trial documents. In our international environment you will influence data management, feasibility, site engagement and

Qualifikationen

• MD physician with clinical training and minimum four years of practice.
• Experience in pharma/CRO clinical development preferred.
• Ability to communicate concisely in an international environment.
• Strong analytical, structured and proactive working style.

Aufgaben

• Own the medical content of Clinical Trial Protocols and updates with the trial team.
• Define medically relevant risks and monitor with an integrated plan.
• Provide medical input into Data Management documents and QA checks.
• Contribute to patient information, consent materials and trial SOPs.
• Support feasibility, recruitment plans and medical queries from investigators.

Kenntnisse

MD (Physician)

Clinical practice

English fluency

Analytical skills

Communication skills

Training/presentation skills

Ausbildung

MD / Medical Doctor

Jobbeschreibung

OUR COMPANY

At Boehringer Ingelheim we develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company, we focus on long‑term performance. We believe that, if we have talented and ambitious people who are passionate about innovation, there is no limit to what we can achieve; after all, we started with just 28 people. Now, we are powered by 50,000 employees globally who nurture a diverse, collaborative and inclusive culture.

The Position

The Study Physician role is a critical position within Clinical Development Inflammation, providing readily available, high‑quality medical support and consultancy for global clinical trials. As a qualified and clinically experienced physician, you will contribute to the discovery, development and delivery of innovative medicines for patients and customers while helping to ensure scientific and medical quality throughout trial planning and conduct. In our international environment, you will collaborate with global colleagues and contribute directly to the success of Boehringer Ingelheim.

Tasks & Responsibilities

• One of your key responsibilities will be to own the medical content of Clinical Trial Protocols and updates in line with the Trial Design Outline, working with the CTL, CPL, Patient Safety Physician, Medical Writer and other trial and evidence team members to ensure high medical quality and timely delivery of core trial documents and milestones.
• In regard to risk‑based quality management, you will define medically relevant critical data and processes, assess associated risks, and establish mitigation and monitoring strategies in the Integrated Quality and Risk Management Plan. As medical co‑author of the Clinical Quality Monitoring Plan, you will execute agile and adaptive monitoring using aggregated and near real‑time data, proactively address quality issues, and ensure timely mitigation and escalation.
• Moreover, you will provide medical input into Data Management documentation, including eCRF design, CRF completion guidance, the Data Review Plan, automated and manual data checks, laboratory parameter specifications, Data Transfer Agreements and central laboratory alerts. You will also support the definition, review and assessment of important protocol deviations.
• Furthermore, you will be accountable for the medical content of patient information and informed consent materials, the Trial Level Monitoring Manual, Trial Communication Plan, Trial Training Plan and Trial Statistical Analysis Plan. You will contribute to patient narratives, Clinical Trial Report planning and review, regulatory and Ethics Committee or IRB responses, trial newsletters, and scientific publications where applicable.
• In addition, you will provide medical input into study and site feasibility, patient recruitment and retention plans, respond to medical queries from investigators, CROs and sponsor representatives, maintain the trial FAQ, build networks with experts, contribute to site engagement, and deliver medical training during country feasibility activities, investigator meetings and sponsor trainings.
• You will support Endpoint Adjudication, Data Monitoring Committees, Data Safety Monitoring Boards and Steering Committees, as applicable, by presenting the study’s medical content, answering medical questions and helping to ensure high‑quality data from a clinical quality monitoring perspective.

Requirements

• Physician (MD), ideally with a medical thesis, trained in a clinical setting and with a minimum of four years of active clinical practice; specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology or Emergency Medicine is desirable
• Experience in the pharmaceutical industry or a CRO in medical or project management functions, ideally in Clinical Development; specific experience in Inflammation Clinical Development is preferred
• Ability to communicate directly and concisely and to collaborate effectively with key stakeholders in an international environment
• Pronounced analytical skills combined with a systematic, well‑structured and proactive working style and strong team spirit
• Pronounced presentation and training skills as well as excellent interpersonal, active listening and influencing skills
• Ability to use digital technologies to access information, communicate, navigate and learn, and to apply creativity and innovation when solving problems; fluency in written and spoken English

As part of our commitment to transparency and fairness, salary information will be shared during the recruitment process. We also offer a comprehensive benefits and wellbeing package.

Applications from persons with severe disabilities are warmly welcomed. In cases of equal qualifications, such applicants will be given preferential consideration in the selection process.

With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.

Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.

Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you’ll be helping to transform lives for generations.