Study Physician

Boehringer Ingelheim; Newell Green; On-site; GBP 90,000 - 130,000; Full time

Job summary

Boehringer Ingelheim in the United Kingdom seeks a Study Physician to provide medical leadership across global clinical trials, from design through reporting, in collaboration with cross-functional teams to ensure patient safety and scientific excellence.

You will contribute to protocols, CQMP, data review, risk management, and regulatory responses, with MD and at least 4 years of clinical practice; experience in inflammation development is preferred.

Qualifications

• MD with a minimum of 4 years' clinical practice experience.
• Specialization in Pulmonology, Immunology, Internal Medicine, or related fields is desirable.
• Experience in inflammation clinical development is preferred.
• Knowledge of clinical development and ICH-GCP regulations.

Responsibilities

• Provide medical leadership across clinical trials, from design to reporting.
• Contribute to protocol development and medical input into trial documentation.
• Support risk-based quality management and monitoring activities.
• Collaborate with internal and external stakeholders to ensure data integrity and patient safety.

Skills

Medical leadership

Stakeholder management

ICH-GCP familiarity

Data interpretation

English communication

Education

MD (Medical Degree)

Job description

At Boehringer Ingelheim, we are united by a shared purpose: transforming lives for generations through breakthrough healthcare innovation. We are seeking a highly motivated Study Physician to join our Global Clinical Development Therapeutic Areas team. In this critical global role, you will provide medical leadership and oversight throughout the lifecycle of clinical trials, from study design and planning through execution, analysis and reporting. As a core member of cross-functional Trial Teams and Evidence Network Teams, you will ensure the highest standards of medical quality, patient safety and scientific excellence across international clinical development programmes. You will collaborate with internal and external stakeholders worldwide, contributing to the successful delivery of clinical studies that support the development of innovative medicines for patients,

• Responsible for medical content of Clinical Trial Protocols (CTPs), in line with TDO, in collaboration with CTL, CPL, Patient Safety Physician, Medical Writer and other trial and evidence team members to ensure high medical quality CTP.
• Responsible for medical input into CTP updates.
• 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 in the Integrated Quality and Risk Management Plan (IQRMP) as well as in risk discussions during trial conduct.
• Medical responsibility as co-author for development of a robust Clinical Quality Monitoring Plan (CQMP) in line with the critical data, medical quality risks and related monitoring/ mitigations identified in IQRMP.
• Responsible for providing medical input into definition of important protocol deviations (iPD), providing input for compilation and review of trial iPD list from medical perspective, and support trial team in deciding on iPDs from identified potential iPDs.
• Responsible for execution of relevant clinical quality monitoring for Study Physician using aggregated data outputs as per trial CQMP, timely mitigation & escalation of identified risks & quality issues.
• Takes medical responsibility for agile & adaptive risk based Clinical Quality Monitoring of critical data.
• Supports close to real time clinical data medical oversight by using advanced technologies and systems.
• Proactively addresses/communicates clinical quality issues in a collaborative environment.
• Contributes to the timely preparation of medically relevant core trial documents and timely milestones.
• Responsible for medical input into Data Management documentation for the trial, such as eCRF design by efficient translation of medical questions into electronic data capturing.
• Responsible for medical input into "Information for CRF completion" (ICC), Data Review Plan (e.g., propose items such as data screening rules for automated data queries, automated or manual data checks for clinical data consistency), laboratory parameters specifications for the project, Data Transfer Agreement, central laboratory alerts etc.
• Responsible for the medical content of Patient Information and Informed Consent, Trial Level Monitoring Manual, Trial Communication Plan, Trial Training Plan, Trial Statistical Analysis Plan (TSAP) etc.
• Responsible for medical contribution to Patient Narrative preparation, Clinical Trial Report planning and review of medical sections of Clinical Trial Report.
• Contributes to the medical content of responses to questions from regulators and Ethic Committees/IRBs.
• Responsible for medical input to study and site feasibility in planning and execution, patient recruitment, and retention plans.
• Responds to medical queries from Investigators, CROs and/or Sponsor team representatives and contributes to maintenance of trial FAQ log/list.
• Builds network with experts and active contribution to site engagement.
• Supports Endpoint Adjudication (EA), Data Monitoring Committee (DMC), Data Safety Monitoring Boards (DSMB) and Steering Committees (SC) (as applicable), by presenting medical content of study to the respective committees, responding to medical questions and by ensuring good quality of data from CQM perspective.
• Provision of medical training at Country feasibility training, Trial Investigators Meetings or to Sponsor staff.
• Responsible for medical review of and contribution to the content of Trial Newsletters.
  Medical Degree (MD) with a minimum of 4 years' 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 pharmaceutical, CRO or other relevant medical environments.
• Knowledge of clinical development and ICH-GCP regulations.
• Strong analytical, communication and stakeholder management skills.
• Ability to work effectively within global cross-functional teams.
• Excellent written and spoken English.
• Experience in clinical trials, medical monitoring or data review would be advantageous.
  Boehringer Ingelheim has been recognised as a Top Employer in the UK, demonstrating our commitment to building an exceptional workplace through strong people practices and supportive HR policies.