Medpace

Small Molecule Bioanalysis Scientist

Medpace$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
  • Experience in analyzing small molecule drugs and metabolites.
  • Strong skills in project management, compliance, communication, and leadership.
  • Familiarity with extraction methods like LLE, SPE, SLE+, and immune-capture hybrid extraction.
  • Hands-on experience with analytical techniques such as LC-MS/MS, GC-MS, ICP-MS, HPLC.
  • Preferred experience in Good Laboratory Practices (GLP).

Responsibilities

  • Develop and validate methodologies for small molecules and biomarkers using various analytical techniques.
  • Draft and organize study protocols and reports.
  • Oversee all phases of bioassay management for pharmacokinetics and biomarker analysis.
  • Manage and guide technicians during method development and validation.
  • Liaise with internal teams and external partners regarding sample management and quality assurance.

Benefits

  • Flexible work environment.
  • Starting PTO at 20+ days.
  • Competitive overall benefits package.
  • Company-sponsored employee appreciation events.
  • Employee health and wellness programs.
  • Community involvement opportunities with local organizations.
  • Discounts on local sports events and attractions.
  • On-site fitness center within eco-friendly campus.
  • Structured career development paths.
  • Tuition discounts for UC online programs.
Full Job Description
Job Summary

Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Analytical Chemistry Scientist to join our Bioanalytical Lab team. This position will work on a team to accomplish tasks and projects that are instrumental to the company's success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

  • Develop and validate LC-MS/MS, GC-MS, ICP-MS, HPLC methods for small molecule drugs or drug metabolites and biomarkers;
  • Draft study protocols/plans, acquisition methods, and study reports;
  • Supervise all phases of bioassays to support pre-clinical and clinical pharmacokinetics, PD Biomarkers;
  • Supervise technicians for performing method development, validation, and sample analysis;
  • Communicate with internal and external resources for sample receiving, quality control, quality assurance, sponsor correspondence etc.


Qualifications

  • PhD in Chemistry, Biochemistry, Pharmaceutical Sciences or related field;
  • Previous experience with small molecule drug and drug metabolites analysis;
  • Strong project management, compliance, communication, and people skills;
  • Experience with various extraction procedures, such as LLE, SPE, SLE+, immune-capture hybrid extraction, etc.;
  • Experience with LC-MS/MS, GC-MS, ICP-MS, HPLC, etc.;
  • Direct working experience in Good Laboratory Practices is preferred.


What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

About Medpace

Medpace is a clinical research organization that provides services to pharmaceutical, biotechnology, and medical device companies. The company's services include clinical trial management, regulatory consulting, and medical imaging. Medpace was founded in 1992 and is headquartered in Cincinnati, Ohio. The company has operations in North America, Europe, and Asia.
Learn more about Medpace
Size
4,700 employees
Market Cap
$6.4 billion
Industry
Net Income
$145.3 million
Founded
1992
5 Year Trend
+22.1%
Revenue
$925.9 million
NASDAQ

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