Scientist Ii, Non-clinical Drug Safety-us

4 weeks ago

Ridgefield, United States BI Pharmaceuticals, Inc. Full time

Performs routine lab duties with mínimal supervision. Participates/assists in the design and execution of non-routine experiments using the Pristima LIMS system. Functions as one of the Pristima LIMS administrators. Performs all work in conformance with applicable regulations. Performs all work in a safe manner. The scope of responsibility is primarily within the laboratory environment and immediate discipline. 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.

**Requirements**:

- Bachelor´s Degree with 3+ years’ experience in related scientific discipline or Master´s Degree in related scientific discipline or equivalent experience in related field
- Demonstrate knowledge of field such as nonclinical development highly preferred
- Able to draft portions of technical reports and SEND datasets highly preferred
- Concise and accurate reporting of technical data and information
- Ability to troubleshoot
- Written and verbal communication skills
- Appropriate level of understanding of applicable regulations
- For Clinical Pathology, Certification (e.g. A.S.C.P. or equivalent) is highly desirable

**Desired Skills, Experience and Abilities**
- Non-clinical Drug Safety LIMS User
- User of Pristima Application
- Experience in toxicology operations, study design and conduct

**Duties & Responsibilities**:

- Initiates and completes routine procedures in an independent and efficient manner, with mínimal supervision; Independently operates and is responsible for Pristima LIMS administration; Troubleshoots effectively
- Demonstrates technical ability to assist in the design and execution of non-routine experiments in Pristima LIMS with supervision
- Applies basic scientific principles with mínimal guidance; Performs literature searches and extracts relevant information from published protocols
- Creates and stores SEND datasets in the BI EDMS
- Demonstrates the ability to interpret outcome of experiments and to propose appropriate follow-up
- Communicates own work effectively orally and in writing; Contributes to writing protocols, procedures, and technical reports; Provide input for scientific reports
- Reports and treats data with a high level of integrity and ethics
- Complies with applicable regulations, performing all work in a safe manner; Maintains proper records in accordance with SOPs and policies

**Compensation Data**:

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