Ad Details
Location:
Description
job title senior scientist, toxicology
autoreqid 96718br
job family scientists
job category full-time
job classification experienced/established
division global pharmaceutical r and d
shift first
relocation assistance within country
overview
at abbott, we provide the perspectives and experience necessary to translate science into real solutions for patients in over 130 markets worldwide.
job description primary job function:
this position is in the toxicology line function wihtin the preclinical safety group and will report to the director, associate director or a sr.
apply external scientific and regulatory inforamtion to development strategies and business practices.
discover a world of opportnuities at abbott.innovative thinkers who are passionate about the work they do, abbott employees are representative of the diversity of the patients we strive to serve every single day across the globe.accurately identify key scientific findings and effecitvely communicate findings in reports, presentations, and meetings.through our diverse healthcare businesses, we connect people and potential in ways that no other company can.maintain a high level of productivity in the lab.
support submissions to global regulatory agencies for drugs in development.publish research in peer-reviewed journals and present work at scientific conferences.
core job responsibilities:
act as glp study director for internally conducted studies and external sponsor monitor for studies conducted at contract research organizations.
education requirements phd and 3+ years of experience.the role may also include activities as a lead scientist in his/her area of expetrise on one or more projects.group leader in toxicology. effective writer and communicator of research or other regulatory materials. we believe that diversity drives innovation,
eeo statement:
at abbott.conduct and report toxicology studies appropriate to ovearll development plans and aligned with regulatory expectations,
design.demonstrate the ability to resolve key proejct hurdles and assumtpions by effectively utilziing avaialble inforamtion and techincal expetrise. proacitvely seek out new information in the litearture and incoroprate this into indiivdual proejct(s) as well as the overall prorgam.
respnosible for proejct scinece within his/her area of expertise on one or more proejct temas. sezie opportunities to pusrue project relevant leads that are in line with the group\'s strategy.
position accountability / scope:
responsible for good laboratory practice compliance and abbott records management within assigned studies and related departmental activities.demonstrate the ability to resolve study design and regulatory issues and key project hurdles and assumptions by effectively utilizing available information and technical expertise. national and international accolades, il
employer of choice
through numerous local,
significant work activities & conditions keyboard use (greater or equal to 50% of the workday)
percent of travel 0 - 20 %
country united states
state/province illinois
site location lake county, abbott is regarded as an employer of choice for our commitment to workplace excellence.today, 000 employees are doing work that matters, abbott\'s nearly 90.with challenging opportunities and work that makes a difference, our employees are given the tools to succeed, lead and grow.conducts and reports glp toxicology studies in support of drug submissions to regulatory agencies, this role designs.effective writer and communicator of research or other regulatory materials. proactively seek relevant information in the literature and incorporate this into knowledge of toxicology practices and overall program issues.
skills/experience requirements basic qualifications:
responsible for glp and nonglp study conduct and project science within his/her area of expertise on one or more project teams. committees and other assignments,
serve as scientific expert for studies, during audits and on project teams.
Contact Now