Study Director III - Safety Pharmacology
Company: Laboratory Corporation
Location: Madison
Posted on: October 10, 2024
Job Description:
If you enjoy inspiring others and leading by example, take your
career to the next level at Labcorp as a Study Director III
specializing in Safety Pharmacology and join our team in Madison,
WI. Our work in developing new pharmaceutical solutions has an
incredible impact on millions of lives worldwide. Be a part of this
life-saving work!Position Summary:Serves as Study Director,
Contributing Scientist/Principal Investigator (providing expertise
in electrocardiography, cardiovascular, respiratory, or central
nervous system subject matter), on pharmacology or toxicology
studies according to the protocol/study plan, Standard Operating
Procedure(s), and to the highest possible scientific standards. Has
overall responsibility for the technical conduct of a study,
coordinates efforts of the study team, leads the interpretation,
analysis, documentation and reporting of results. Activities also
include productive interactions with management, technical staff,
global internal and external clients, and study direction staff,
and performing a mentoring/scientific lead role that may include
formal management/matrix management structure.Candidates given best
consideration will have the following qualifications:
- 5 to 7 years of related experience including expertise in
GLP-compliant nonclinical laboratory studies.
- Ability to maintain current regulatory awareness (domestic and
foreign).
- Ability to accurately read, record, and communicate information
to study direction, supervisor, team members, clients, and
vendors.
- Ability to thrive as a leader in a matrix management structure;
demonstrate a positive attitude and mentor novice team members,
technical staff, and cross site personal.
- Ability to lead projects with little supervision and
directive.
- Highly skilled in conducting research, data interpretation, and
report writing.
- Excellent people skills.Essential Job Responsibilities:
- Provides excellent customer care to both internal and external
clients, including timely production of high-quality protocols,
compiled study progress updates, reports, and other client
deliverables.
- Liaises with sponsors and other customers in a timely and
professional manner on study related matters. Participates in and
may host customer visits.
- Maintains oversight of data analysis; provides scientific
guidance to technical staff and study scientists to ensure accuracy
and compliance with protocols and SOPs, and maintains accurate
records of all laboratory work performed, in accordance with the
standards of GLP. Maintains (and meets) study and report dates and
other agreed information on the Master Schedule.
- Maintains an up-to-date knowledge and understanding of the
industry position on related pharmacology disciplines to provide
credibility and confidence to clients.
- Evaluates and interprets nonclinical data from pharmacology
studies/fully interpret pharmacology study results.
- Presents projects internally or externally at professional
meetings/peer reviewed literature.
- May serve as department lead for certain clients/product
lines/therapeutic areas.
- Maintains awareness of study financial status and initiates
additional work order notices to ensure study costs match changes
to study design.
- Identifies opportunities for process improvements, takes
ownership of process, and drives process improvement to completion.
Participates on other process improvement teams.
- Participates in multi-site harmonization/quality projects.
- Performs a leadership/mentoring/scientific lead role that may
include formal management/matrix management structure.Education:
- Ph.D., DVM, or equivalent degree. Experience may be substituted
for education.
- Board certification in a relevant scientific specialty (e.g.,
DABT, DSP) desirable.Benefits: Employees regularly scheduled to
work 20 or more hours per week are eligible for comprehensive
benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k),
Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition
Reimbursement and Employee Stock Purchase Plan. Casual, PRN & Part
Time employees regularly scheduled to work less than 20 hours are
eligible to participate in the 401(k) Plan only.Why People choose
to work at Labcorp:At Labcorp, it is our people that make us great
- it's what our clients, our partners and, most importantly, what
our employees say. Here, you will have the opportunity to
collaborate with extraordinary people with diverse viewpoints. You
will discover your own outstanding potential as we build an even
stronger organization with industry leaders from early development
to the clinic and beyond. We help our clients develop medicines
that improve health and improve lives of their family and
friends.Labcorp is proud to be an Equal Opportunity Employer:As an
EOE/AA employer, Labcorp strives for diversity and inclusion in the
workforce and does not tolerate harassment or discrimination of any
kind. We make employment decisions based on the needs of our
business and the qualifications of the individual and do not
discriminate based upon race, religion, color, national origin,
gender (including pregnancy or other medical conditions/needs),
family or parental status, marital, civil union or domestic
partnership status, sexual orientation, gender identity, gender
expression, personal appearance, age, veteran status, disability,
genetic information, or any other legally protected
characteristic.We encourage all to applyIf you are an individual
with a disability who needs assistance using our online tools to
search and apply for jobs, or needs an accommodation, please visit
our or contact us at .For more information about how we collect and
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Keywords: Laboratory Corporation, Palatine , Study Director III - Safety Pharmacology, Executive , Madison, Illinois
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