Be an early applicantLess than 25 applicants

Company

Original Job Post

myGwork - LGBTQ+ Business Community · 3 days ago

Scientific Coordinator (Toxicology)

Reno, NV

Full-time

Onsite

Entry Level

$23/hr - $23/hr

1+ years exp

Wonder how qualified you are to the job?

Maximize your interview chances

Internet

Insider Connection @myGwork - LGBTQ+ Business Community

Discover valuable connections within the company who might provide insights and potential referrals, giving your job application an inside edge.

Responsibilities

Create/customize planning tools to facilitate prioritization of daily activities.

Basic sponsor visit support including drafting the agenda and collecting requested study/facility data.

Train to create Protocol Amendment shell for use by SC III and higher.

Facilitate signature/approval process for protocol, amendments and other required forms.

Posting and shipping of Protocols and Protocol Amendments.

Schedule pre-study meetings and data review meetings.

Train to extract information from protocol and study data to generate the materials and methods sections of preclinical study reports.

Train to create data tables for report from automated data collection systems or manual data if applicable.

Assist SC II, and higher to maintain reporting timelines.

Assist with management of QA audits and assure necessary corrections and follow-up take place.

Ensure that all study books are corrected appropriately, and that documentation is GLP compliant prior to submission to QA.

Train to assist in documentation of deviations from the protocol or Standard Operating Procedures (SOP).

Posting and shipping of Protocols and Protocol Amendments.

Train to assist in transcription of sponsor comments into the report.

Work closely within a small team environment.

Under direction of the study director, receive, review and accept proof corrections from report coordination staff and make recommended corrections as appropriate.

Provide editorial/formatting review of final study protocols, amendments and report text. Provide comments and/or suggested changes to study director.

Upload data/reports to CR Sponsor portal and/or Sponsor portal.

Perform all other related duties as assigned.

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

Scientific processesComputer skillsMs office softwareDatabase managementMedical terminologyTechnical aspects of research studiesObserving dosingSurgical proceduresNecropsy evaluationsAnalytical thinking organizationalAttention to detail

Required

Education: High School Diploma or GED. Associates (AA/AS) or Bachelors (BA/BS) in a scientific discipline preferred, but not required.

Experience: 1-3 years related experience preferred; but not required in a laboratory or scientific research environment.

An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above.

Certification/Licensure: None.

Other: This position requires analytical thinking skills and a good understanding of scientific processes. Strong organizational skills and attention to detail required, as are computer skills including MS Office software and database management. Must be familiar with medical terminology and have a thorough understanding of technical aspects of research studies (e.g. observing dosing, treatments, surgical procedures, and necropsy evaluations).