Job Information
Boehringer Ingelheim US_Research Biologist, Clinical in Fulton, Missouri
Description
The Research Biologist, Clinical participates as required in Clinical Research and Development studies. The main focus of this position will be technical laboratory and animal work (e. g., parasite isolation and propagation; support to animal model development; inoculation of animals; injections, blood sampling, necropsy, parasite counts, observations, etc.). The individual will be responsible for parasitology models – establishment, development and maintenance to evaluate safety and efficacy in the target species for new animal pharmaceutical research and development projects, line extensions and maintaining existing licensed products. The individual will act as a Clinical Representative as assigned for all stages of parasite propagation, serving as a subject matter expert in representing his/her function (e.g. endo or ecto parasite propagation). The Research Biologist will coordinate 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. As needed, the Research Biologist can participate in other administrative tasks related to study programs.
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
With guidance, performs study procedures as assigned, involving inoculation of trial animals with organisms (parasites, bacterial inoculum, etc.), administration of experimental material, blood sampling, necropsy, health observations, etc. The incumbent also contributes to the implementation of animal models in either the target or surrogate animal species and to general in vitro and/or ex vivo study procedures as required.
Responsible for the development of laboratory techniques, ensuring accurate and timely laboratory service in support to the conduct of clinical studies.
With guidance, contributes to parasitological, microbiological, cell culture or analytical processes based on analysis of data gathered during studies or process/method/animal model development.
Participates as a member of the Clinical R&D team by assisting in the origination of the study protocol, conducting pre-study and ongoing study functions including, but not limited to, designing of study report forms, notebook preparation, data collection, initiating calendar of events and other technical/administrative study-related functions as needed.
Assists with the creation of site-specific technical SOPs ensuring adherence to legal and corporate biosafety/biosecurity and animals welfare regulations.
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.
Mentor, coach and train colleagues as necessary.
Complies with all applicable regulations governing the Animal Health Industry (GCP, GLP, Animal Welfare, Regulatory requirements, etc.). Ensures that work performed in area of responsibility is conducted in a safe and compliant manner. Maintains proper records in accordance with SOPs and policies.
Requirements
B.S. degree (preferred), or Associate's degree, or equivalent from an accredited institution in an area related to biology; or three (3) years of experience related to animal research.
Laboratory experience is a plus.
A basic level of animal handling experience is required.
Good verbal and written communication skills (correspondence, protocols, reports, etc.).
Must rapidly assimilate knowledge of GCP/GLP regulations and Boehringer Ingelheim Animal Health procedures as necessary.
Knowledge and skills with Microsoft Office (Microsoft Word and Excel) and ability to learn Clinical and Laboratory Data Management System software.
Strong organization skills and attention to detail are essential.
Must be able to collect and handle data to meet GxP, GCP, and GLP requirements.
Must be able to work directly with both target animals and pathogens.
Must be familiar with and ensure for compliance with legal and corporate biosafety/biosecurity procedures.
Good interpersonal skills.
A collaborative team player.
Possesses a customer service orientation, delivering results and executing in a fast and focused manner.
Good organizational skills with quality orientation.
Effective time management.
Ability to work with some level of independence.
High degree of attention to detail. Ability to find errors or inconsistencies others may miss.
Exhibits integrity and trust.
Desired Skills, Experience and Abilities
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.