At a Glance
- Tasks: Lead medical oversight in clinical trials, ensuring patient safety and scientific excellence.
- Company: Join Boehringer Ingelheim, a top employer committed to healthcare innovation.
- Benefits: Enjoy a hybrid work model, career development opportunities, and a supportive workplace culture.
- Other info: Collaborative environment with strong focus on employee wellbeing and professional growth.
- Why this job: Make a real impact on patients' lives through groundbreaking healthcare solutions.
- Qualifications: Medical Degree (MD) with clinical experience; specialisation in relevant fields preferred.
The predicted salary is between 75600 - 92400 £ per year.
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.
Location: Bracknell, UK, with a hybrid working model requiring a minimum of 2 days per week in the office.
Tasks And Responsibilities
- 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, 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.
Requirements
- 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.
WHY THIS IS A GREAT PLACE TO WORK
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.
To learn more about why BI is a great place to work, visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
Our Company
Why Boehringer Ingelheim? 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.
Want to learn more? Visit https://www.boehringer-ingelheim.com
Study Physician in Bracknell employer: Boehringer Ingelheim
Boehringer Ingelheim in Pirbright offers a dynamic work environment where innovation and compliance are at the forefront of our operations. As a leading player in the pharmaceutical industry, we provide our employees with robust growth opportunities, a supportive culture that values teamwork, and a commitment to quality that empowers you to make a meaningful impact. Join us and be part of a company that prioritises your professional development while contributing to the health and well-being of communities worldwide.
StudySmarter Expert Advice🤫
We think this is how you could land Study Physician in Bracknell
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Check out associations like the Institute of Healthcare Management. They often have job boards, networking events, and conferences that are perfect for connecting with potential employers in health sciences administration.
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We think you need these skills to ace Study Physician in Bracknell
Some tips for your application 🫡
Highlight Your Relevant Experience:When applying for a role in health sciences administration, it's super important to spotlight any relevant experience you have in healthcare settings. Whether you've worked in a hospital, a clinic, or any related environment, make sure to detail those roles in your CV – focusing on your responsibilities and achievements that align with the job at Boehringer Ingelheim.
Showcase Your Administrative Skills:Administrative skills are key in this field, so don’t hold back! Make sure your CV reflects your proficiency in things like scheduling, data management, and compliance with health regulations. Mention specific software you’ve used, such as patient management systems, as this will demonstrate your hands-on abilities and readiness for the role at Boehringer Ingelheim.
Craft a Meaningful Cover Letter:Your cover letter should reflect your passion for the health sciences field and your eagerness to contribute to Boehringer Ingelheim. Share a bit about why you’re drawn to this sector, any impactful situations or challenges you’ve encountered, and how they’ve shaped your desire to work in health sciences administration. This personal touch can really set you apart!
Tailor Your Documents to the Job:Don't use a one-size-fits-all approach! Make sure your CV and cover letter are specifically tailored for this role. Highlight any certifications you have relevant to health administration, and ensure you clearly connect your previous roles to the skills needed for the full-time position at Boehringer Ingelheim. This way, you're showing them you’ve done your homework and are genuinely interested in being a part of their team.
How to prepare for a job interview at Boehringer Ingelheim
✨Showcase Your Administrative Skills
In health sciences administration, being organised is key. Make sure you can demonstrate your skills in managing schedules, paperwork, and data accurately. Be ready to discuss specific tools you've used, like electronic health record systems or scheduling software, and how they improved efficiency in your past experiences.
✨Know Your Regulations
Familiarity with healthcare regulations and compliance is crucial. Brush up on HIPAA, GDPR, or other relevant policies before your interview. We recommend preparing examples of how you've ensured compliance or handled sensitive information in past roles—this will show you're not just knowledgeable but also responsible.
✨Prepare for Scenario Questions
Interviews for administrative roles often involve scenario-based questions to assess your problem-solving skills. Practice responses to common situations you might face, such as dealing with a challenging patient or managing a sudden schedule change. This will not only demonstrate your ability to think on your feet but also highlight your interpersonal skills.
✨Align Your Goals with the Organisation
As a full-time candidate, employers will want to know how your long-term career goals align with their mission. Take some time to research Boehringer Ingelheim’s values and be ready to tie your passion for health sciences administration into their objectives. Demonstrating enthusiasm and career alignment can be a game-changer in this competitive field!
