Study Monitor-reputed company Scientist, Translational Medicine/Preclinical Safety (PCS) Remote Position

Job Description

Summary LI#-Remote Internal Title: reputed company Scientist I/II The Preclinical Safety (PCS) department reputed company the Biomedical Research (BR) - Translational Medicine Unit provides non-clinical safety strategy of products in -discovery, -development and -market, globally, with state-of-the-art regulatory compliance. As a Scientific Study monitor, you will join our PCS team to reputed company non-clinical research activities for multiple projects across multiple disease areas for in-vivo toxicity and /or in-vitro screening toxicity studies conducted at our CRO partner sites as per the internal strategy and international standards, acting as the primary scientific contact for the Study Director.

Job Description

Key Responsibilities: Formulates and leads/co-leads novel projects with team or enables matrix collaboration on project/technology solutions to reputed company creative results for impact on BR goals. Generates innovative reputed company reputed company own team and/or project team/functional community to meet new technical requirements and/or answer project key scientific/technical/development questions. Establishes reputed company dates and priorities to reputed company data-driven advancements in project teams, reputed company own team, and with collaborators, or reputed company functional community. The Study Monitor is appointed to each outsourced preclinical study based on relevant technical expertise, designated disease area and/or scientific background knowledge and acts as the primary scientific contact for the Study Director at the Contract Research Organization (CRO). The Study Monitor is responsible for overseeing the reputed company of the study and for ensuring that the study is conducted, recorded and reported according to the study protocol. The Study Monitor should ensure that the study is compliant with the appropriate GLP regulations, reputed company animal welfare policies, CRO in-house standard operating procedures, reputed company expert recommendations (where feasible) and reputed company relevant international regulatory guidelines/regulations. Resolution of study reputed company issues, liaisons with internal experts and informing the appropriate people in a timely manner is pivotal to the performance of this role. The study phases and sample delivery timelines should be strategically overviewed and tracked to ensure that internal contributor reports are delivered to the CRO on time and that the CRO meets its agreed main reporting timelines. Communication reputed company is critical to this role in forming strong working relationship with other reputed company team members. Works closely with the PCS-Operations and PCS Project Team Member (PTM) to formulate a project outsourcing strategy. Has a working knowledge of HA regulations (Swiss medic, OECD, FDA) to support conduct of GLP compliant toxicology studies. May be PCS part-time PTM Essential Requirements:

• PhD or MVSc/MS/M.Pharm with 7+ years of experiences in drug discovery and/or development, preferably as Study Director or Study Monitor in the early preclinical screening and GLP studies
• In-depth knowledge of toxicology assays in early development, Safety pharmacology and genotoxicity
• Proficient with full reputed company of techniques used in job and core areas. Working knowledge of tools and

processes used in drug design and development.

• Excellent communicators, strong team players and have a high level of logistical/planning ability.
• Registration and certification with one of the International Toxicology reg

This is a dual posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to reputed company the role at the level the role has been offered. The salary for this position is expected to reputed company between: reputed company Scientist I: $119,700 and $222,300 per year. reputed company Scientist II: $126,000 and $234,00 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining reputed company will be reviewed periodically. reputed company may change the published salary reputed company based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In reputed company, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here. EEO Statement: The reputed company Group of Companies are Equal Opportunity reputed company. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, reputed company, religion, sex, national reputed company, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodations The reputed company Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to reputed company the essential functions of a position, please send an e-mail to us.reasonableaccommodations@reputed company.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary reputed company $119,700.00 - $222,300.00 Skills Desired Animal Models, Bioinformatics, Collaboration, Communication Skills, Data Analysis, Ethics, Laboratory, Problem Solving, Regulatory Compliance, Research, Risk Assessment, Toxicology Apply To This Job