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US_SR Scientist, Clinical at Boehringer Ingelheim

US_SR Scientist, Clinical

Boehringer Ingelheim Saint Joseph, MO Full-Time



Responsible for the safety and efficacy in the target species for new animal pharmaceutical research and development projects, line extensions and maintaining existing licensed products. Provides clinical study design and implementation including resource and budget planning from protocol to execution and to final study report for submission to regulatory agencies for animal pharmaceutical projects in both lab and field conditions. Fulfills a role as a subject matter expert in representing his/her function (e.g. on development teams, regulatory authority meetings and key Opinion Leaders). Acts as the Clinical Representative as assigned for all stages of product development. Presents clinical content to regulatory authorities as required and ensures compliance with all applicable regulatory and animal welfare principles. The incumbent may lead a Clinical Team as Clinical Leader and is responsible for development and implementation of the clinical strategy. The Clinical Leader serves as the representative on the Core Team.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

Duties & Responsibilities\:

  • Independently initiates and coordinates strategic scientific experiments with a predefined goal including developing new methodologies, protocols and/or test procedures that contribute to innovation and core group/research goals and reflect expert knowledge. Responsible for overall study design, execution, and reporting to achieve project milestones. Designs clinical studies to earn label claims and new product licenses/marketing authorizations consistent with the TPP and in compliance with global regulatory guidance and corporate standards for data integrity and animal welfare. May direct and oversee experimental study design and data analysis/results of junior-level scientists.

  • Demonstrates expertise in a specific project-relevant area or technology. May provide guidance and expertise to advance specific projects or evaluate and propose new technologies and concepts in support of multiple projects. Keeps abreast of relevant literature. Develops visibility outside of functional area and effectively interacts scientifically with Key Opinion Leaders in relevant fields of research. Publishes research in peer reviewed journals and presents data at national/international meetings as requested.

  • Skillfully collaborate across functions (internal and external stakeholders)  to assure clinical plans and activities for project teams are delivered efficiently, while supporting continuous improvement in quality including, speed and value of processes supporting studies including protocol and forms, test article availability & suitability, monitoring effectiveness, statistical analysis, study event tracking, compliance, and excellent reporting.

  • Develops and leverages external providers, academia and Contract Research Organizations as necessary.

  • Mentor, coach and train colleagues, especially research associates/monitors, on best practices for study execution with flawless speed and compliance, professional & collaborative team member behaviors, accountability, and alignment within Pharma Clinical and with all stakeholders. Assumes responsibility for direct reports, if assigned and as needed, including recruiting, managing, mentoring and developing scientific staff.

  • Provide technical content (safety and efficacy data) for local and international regulatory submissions and/or leads clinical discussions in authority meetings and/or develops clinical and regulatory strategy.

  • Develops the clinical strategy and works effectively toward achieving the project goals as defined in the TPP. The individual assumes leadership (as the clinical leader or clinical representative) for clinical programs within multi-disciplinary Project Teams for the effective research and development of pharmaceutical projects. Interacts with Project Leaders, members of the Project Teams and stakeholders. Responsible for clinical project progress, including timelines, deliverable and budgetary responsibilities. Ensures that risks and changes to the Target Product Profile (TPP) are communicated into the project team. The individual provides clinical input to the TPP and influences the Project from the clinical veterinary and scientific perspective.

  • Takes  on Study Director, Monitor and Investigator roles as necessary. Responsible for the design, organization, conduct, timely completion and reporting of assigned clinical R&D studies in order to establish safety and efficacy of new pharmaceuticals, and to develop new claims and uses for existing products.

  • Ensures compliance in the area of GLP, GCP, PV, animal welfare and local regulatory requirements. Study Director responsibilities are described in the applicable GLP standards.

  • Contribute or lead internal initiatives such as SOP development, patent filings and due diligence.


  • DVM or PhD from an accredited institution plus five (5) years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization.

  • In lieu of DVM, will accept PhD from an accredited institution with significant experience in a veterinary-relevant field such as parasitology or animal nutrition, plus five (5) years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization.

  • In lieu of DVM or PhD, will accept a Masters Degree from an accredited institution with significant experience in a veterinary-relevant field such as parasitology or animal nutrition, plus ten (10) years of experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization.

  • Board Certification and/or advanced degree (MS or PhD) in addition to DVM is a plus.

  • A minimum of five (5) years of broad experience in a related field with a proven track record of successfully implementing or investigating technologies and adding value to the organization or equivalent combination of education and experience.

  • Considerable experience (greater than three (>3) years) in veterinary research & development.

  • Experienced in project/program management; one to three (1-3) years leading projects.

  • Hands-on experience with clinical and laboratory/field studies (GxP and non GxP)

  • Experience in analyzing literature and technology trends in the veterinary and pharmaceutical industry.

  • Experience with planning, conducting, reporting, analyzing and interpreting clinical studies.

  • Research methodology experience.

  • Clinical veterinary practice experience is preferred.

  • Solid / basic understanding of claim structure of veterinary pharmaceutical products including sound knowledge of the veterinary business environment and how clinical design impacts label language and commercial value of a product.

  • Able to effectively work in an international and cross-functional matrix environment

  • Knowledge of global regulatory requirements (e.g. FDA, EMA) and compliance.

  • Basic understanding of statistical principles in clinical studies.

  • Understands principles of clinical risk assessment and risk mitigation.

  • An analytical thinker.

  • Excellent skills in understanding data and scientific decision processes, and in interpreting and reporting these data in well supported conclusions targeted at achieving project objectives.

  • Strong leadership skills. Able to lead (e.g. the Clinical team) without formal authority.

  • Fosters innovation. A problem solver.

  • Outstanding / Good communication and interpersonal skills.

  • A collaborative team player.

  • Values diversity and inclusion.

  • Possesses a customer service orientation, delivering results and executing in a fast and focused manner.

  • Exceptional planning and organizational skills with a quality orientation. Strives for business process excellence.

  • Accepts accountability and ownership.

  • Exhibits integrity and trust.

  • English\: Fluent (read, write and speak)

  • Demonstrates industry-leading knowledge of field.

  • Ability to communicate effectively both orally and in writing in an inter-disciplinary and international environment.

  • Demonstrated knowledge of the Pharmaceutical life cycle process.

  • Exhibits business and technical knowledge.

  • Willingness to travel.

Eligibility Requirements\:

  • Must be legally authorized to work in the United States without restriction.

  • Must be willing to take a drug test and post-offer physical (if required).

  • Must be 18 years of age or older.

Who We Are\:

At Boehringer Ingelheim we create value through innovation with one clear goal\: to improve the lives of patients. 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 are powered by 50.000 employees globally who nurture a diverse, collaborative and inclusive culture. Learning and development for all employees is key because your growth is our growth.

Want to learn more?  Visit and join us in our effort to make more health.

Boehringer Ingelheim is an equal opportunity global employer who takes pride in maintaining a diverse and inclusive culture. We embrace diversity of perspectives and strive for an inclusive environment, which benefits our employees, patients and communities. 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.

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Job ID: AR02-5950_225251

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