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Study Physician
Boehringer Ingelheim. Provide readily available, high-quality medical support and consultancy for global clinical trials .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial management, medical content development, and quality assurance in clinical research. Proficient in collaborating with cross-functional teams and providing high-quality medical support throughout the trial lifecycle.
Highest-signal resume keywords
Physician (MD)Clinical Trial Protocol DevelopmentClinical Development ExperienceInflammation Clinical DevelopmentFluency in English
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Quality MonitoringData Management DocumentationPatient Recruitment StrategiesProtocol Deviation AssessmentMedical Input for Regulatory Responses
Soft Skills
Analytical SkillsPresentation SkillsInterpersonal SkillsActive ListeningCollaboration
Tools & Technologies
Digital Technologies for CommunicationECRF DesignData Review PlanTrial Communication PlanTrial Training Plan
Industry Keywords
Clinical TrialsPharmaceutical IndustryCROMedical ConsultancyTrial Quality Assurance
About the role
Key responsibilities & impact- Provide readily available, high-quality medical support and consultancy for global clinical trials
- Contribute to discovery, development and delivery of innovative medicines while ensuring scientific and medical quality throughout trial planning and conduct
- Own the medical content of Clinical Trial Protocols and updates in line with the Trial Design Outline
- Collaborate with the CTL, CPL, Patient Safety Physician, Medical Writer and other trial and evidence team members
- Define medically relevant critical data and processes, assess risks, and establish mitigation and monitoring strategies in the Integrated Quality and Risk Management Plan
- Co-author the Clinical Quality Monitoring Plan and execute agile, adaptive monitoring using aggregated and near real-time data
- Proactively address quality issues and ensure timely mitigation and escalation
- Provide medical input into Data Management documentation, including eCRF design, CRF completion guidance, Data Review Plan, data checks, laboratory specifications, Data Transfer Agreements and central laboratory alerts
- Support the definition, review and assessment of important protocol deviations
- Own the medical content of patient information, informed consent materials, Trial Level Monitoring Manual, Trial Communication Plan, Trial Training Plan and Trial Statistical Analysis Plan
- Contribute to patient narratives, Clinical Trial Report planning and review, regulatory and Ethics Committee or IRB responses, trial newsletters and scientific publications
- Provide medical input into study and site feasibility, patient recruitment and retention plans
- Respond to medical queries from investigators, CROs and sponsor representatives and maintain the trial FAQ
- Build expert networks, contribute to site engagement and deliver medical training during country feasibility activities, investigator meetings and sponsor trainings
- Support Endpoint Adjudication, Data Monitoring Committees, Data Safety Monitoring Boards and Steering Committees by presenting study medical content and answering medical questions
- Help ensure high-quality data from a clinical quality monitoring perspective
Requirements
What you’ll need- Physician (MD), ideally with a medical thesis
- Trained in a clinical setting
- 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 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
- 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
- Application documents must be submitted in English
Benefits
Comp & perks- Comprehensive benefits and wellbeing package
- Applications from persons with severe disabilities are warmly welcomed
- In cases of equal qualifications, applicants with severe disabilities will be given preferential consideration