Senior Clinical Scientist, Veterinary Therapeutics

Boehringer Ingelheim; Ames (IA); On-site; USD 90,000 - 120,000; Full time

Job summary

Boehringer Ingelheim is looking for a Senior Scientist in Ames, Iowa. This role involves contributing to the discovery and development of veterinary pharmaceuticals and leading clinical research projects. You will design and execute studies, provide expert guidance, and mentor junior scientists. The ideal candidate will have a DVM or PhD with relevant experience and strong leadership skills.

Excellent communication and problem-solving abilities are essential. This is a unique opportunity to work in a dynamic environment committed to animal welfare and innovative therapeutics.

Qualifications

• 5 years' experience with proven track record in related field.
• Interest in developing therapeutics a plus.
• Experience in research methodology and project management.

Responsibilities

• Initiate and coordinate strategic scientific experiments.
• Design clinical studies supporting label claims.
• Lead internal initiatives like SOP development.

Skills

Strong analytical and problem-solving skills

Excellent scientific decision making

Communication and interpersonal skills

Leadership experience

Education

DVM or PhD in a veterinary-relevant field

Master’s Degree with extensive experience

Job description

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 several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.



The Senior Scientist, Clinical is responsible for the safety and efficacy in the target species for new animal pharmaceutical and biological research and development projects, line extensions and maintaining existing licensed products. This role 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 and biological projects in both lab and field conditions. The incumbent 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).



The Senior Scientist, Clinical acts as the Clinical Representative as assigned for all stages of product development. This role resents 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.

Description

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 several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.



The Senior Scientist, Clinical is responsible for the safety and efficacy in the target species for new animal pharmaceutical and biological research and development projects, line extensions and maintaining existing licensed products. This role 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 and biological projects in both lab and field conditions. The incumbent 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).



The Senior Scientist, Clinical acts as the Clinical Representative as assigned for all stages of product development. This role resents 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.

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 collaborates 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


• Mentors, coaches, and trains colleagues, especially clinical 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


• Provides 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


• 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

Requirements

• DVM preferred with 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 required

OR

• PhD (with significant experience in a veterinary-relevant field such as parasitology or animal nutrition) with 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 required

OR

• Master’s Degree (with significant experience in a veterinary-relevant field such as parasitology or animal nutrition) with 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 required


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


• Clinical veterinary practice experience is preferred


• Interest in developing therapeutics a plus


• Minimum of five years (5) 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


• Demonstrates industry-leading knowledge of field


• 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


• Research methodology experience


• Fosters innovation


• A problem solver


• Outstanding / Good communication and interpersonal skills


• A collaborative team player


• 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


• Willingness to travel (>10% annual travel)


• English: Fluent (read, write and speak)


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


• Leadership experience: One to three (1-3) years leading projects


• Demonstrated knowledge of the product life cycle process


• Experienced in project/program management


• Exhibits business and technical knowledge

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

Desired Skills, Experience and Abilities

Additional Duties & Responsibilites:

• Ensures that risks and changes to either the Research Target Profile (RTP) or Target Product Profile (TPP) are communicated into the project team


• Provides clinical input to the either RTP or TPP and influences the Project from the clinical veterinary and scientific perspective


• Takes on Clinical Lead, Study Director, Monitor and Investigator roles as necessary


• Responsible for the design, organization, conduct, timely completion and reporting of assigned clinical R&D studies to establish safety and efficacy of new pharmaceuticals, and to develop new claims and uses for existing products


• Ensures compliance around GSP, GLP, GCP, PV, animal welfare and local regulatory requirements


• Study Director responsibilities are described in the applicable GLP standards


• Contributes or leads internal initiatives such as SOP development, patent filings and due diligence

Our Company Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry's top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,300 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at www.boehringer-ingelheim.com. 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