Biologist Boehringer Ingelheim 807 reviews - Fulton, MO Responsible for a wide range of duties in support of research trial operations including: assisting in preparing protocols, preparation of research trial notebooks, assists with study procedures as required for data collection, maintaining drug inventories, assisting in data entry, working with an investigator/monitor in preparation of trial reports, preparing data and reports for submission, and assisting with both standard and experimental laboratory assignments as required. 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: * Supports Director II with administration of GLP, GCP, and GSP studies (i.e. clinical supplies inventory, storage and disposal; data capture, data storage; study administration and status reports, draft protocols and reports, grant payments, etc). * Assists Director II with investigator training, study related correspondence, field trial notebook preparation, study set-up and termination, test substance preparation, randomization and logistics, collection and capture of study data, reporting remarkable events, and drafting of study reports. * Assists in data entry in Excel or Clinical Data Management System (under the direction of the Clinical Data Manager). * Prepares and collates trial reports in compliance with GCP/GLP/Merial procedures under the direction of Director II. * Conducts QC review of portions of data, data entry, or trial reports under the direction of Director II, if necessary. * Assists with study procedures as required for data collection. * Maintains and initiates needed data and study forms related to study activity. * Supports other office and laboratory staff, as necessary. * Support the development and maintenance of an efficient and harmonized approach to GCPs / GLPs compliance activities across Clinical Operations. * Is expected to perform all duties in safe manner in accordance with Company guidelines and policy. Requirements: * High School diploma and a minimum of 3 years relevant experience. * B.S., or Associates degree, or equivalent in an area related to biology; or three years experience related to animal research, a plus. * Must rapidly assimilate knowledge of GCP/GLP regulations and Merial procedures. * 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. 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 Our Culture: Boehringer Ingelheim is a different kind of pharmaceutical company, a privately held company with the ability to have an innovative and long term view. Our focus is on scientific discoveries that improve patients' lives and we equate success as a pharmaceutical company with the steady introduction of truly innovative medicines. Boehringer Ingelheim is the largest privately held pharmaceutical corporation in the world and ranks among the world's 20 leading pharmaceutical corporations. At Boehringer Ingelheim, we are committed to delivering value through innovation. Employees are challenged to take initiative and achieve outstanding results. Ultimately, our culture and drive allows us to maintain one of the highest levels of excellence in our industry. Boehringer Ingelheim, including Boehringer Ingelheim Pharmaceuticals, Inc., Boehringer Ingelheim USA, Boehringer Ingelheim Animal Health USA, Inc., Merial Barceloneta, LLC and Boehringer Ingelheim Fremont, Inc. is an equal opportunity and affirmative action employer committed to a culturally diverse workforce - Minority/Female/Protected Veteran/Person with a Disability. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. Boehringer Ingelheim is firmly committed to ensuring a safe, healthy, productive and efficient work environment for our employees, partners and customers. As part of that commitment, Boehringer Ingelheim conducts pre-employment verifications and drug screenings. Job - Research & Development Primary Location - Americas-United States-MO-Fulton Organization - US-Merial, Inc. Schedule