The Position

Passionate about patient health and safety? We have an exciting opportunity for you!

Our dedicated TA CRM Team is looking for an experienced Lead Patient Safety Physician with expertise in cardiovascular, renal, metabolic, and/or respiratory diseases. You'll work on a variety of products, both in clinical development and post-marketing drug safety. Ready to make a real difference in patient safety? We look forward to your application!

This position can be filled in Germany (Ingelheim or Biberach) or in the US (Ridgefield).

If you want to apply for the position in the US, please use this link: Executive Director, Medical Safety (boehringer-ingelheim.com) (https://jobs.boehringer-ingelheim.com/job/Ridgefield%2C-CT-Executive-Director%2C-Medical-Safety-Unit/1019444901/)

If you want to apply for the position in Germany (Ingelheim or Biberach) click "Apply now".

We kindly ask you to apply for the Boehringer Ingelheim location that is closest to your country of residence. Please, do not apply for more than one location!

Tasks & responsibilities

As a Lead Patient Safety Physician, you will:

• Lead, manage, and provide medical-scientific direction to a team of Patient Safety Physicians responsible for a compound/asset, including project management, project-specific guidance, team coaching, and review of team output

• Develop proactive patient-centric risk minimization strategies for assigned assets on a global level

• Enhance the value of BI assets through robust assessment of the benefit-risk profile

• Design evidence strategies that differentiate the asset through its benefit-risk profile, considering the scientific knowledge for the molecule, medical safety landscape, population, regulatory landscape, and patient perspective

• Generate safety evidence and perform safety & efficacy analyses to support decision-making by patients, regulators, HCPs, payors, and HTA bodies

• Review and provide medical-scientific input to regulatory documents (e.g., PSURs, DSURs, RMPs, Clinical Overview Statements)

• Interpret clinical trial safety data for clinical trial reports and submission documents

• Establish strategic partnerships within the Asset and Evidence Network

• Ensure patient safety while adhering to the highest quality and ethical standards

• Represent PSPV in internal and external multidisciplinary committees & bodies

• Contribute to PSPV's development within Boehringer Ingelheim by staying updated on methodology, regulatory changes, and healthcare trends

Requirements

• Medical Doctor with sound clinical and/or clinical research experience

• Profound experience in patient safety at a pharmaceutical company on a global/corporate level, including clinical development and post-marketing safety

• Comprehensive understanding of pharmacovigilance regulations in major markets and the need for compliance

• Broad understanding of the pharmaceutical industry, and interest in future trends and developments in pharmacovigilance

• Clinical or research experience in the cardio-renal-metabolic field

• Leadership, people management & project management skills

• Excellent collaboration, communication, and negotiation skills

• Strong ethical sense with a quality and patient safety mindset

• Fluent in English, both written and spoken

*Ready to contact us? *

If you have any questions about the job posting or process - please contact our HR Direct Team,

Tel: +49 (0) 6132 77-3330 or per mail: hr.de@boehringer-ingelheim.com

Recruitment process: Recruitment process:

Step 1: Virtual meetings starting mid of March 04th, 2024

Step 2: On-site interviews starting in beginning of May, 2024

All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.