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IQVIA

Runs drug trials and sells health data to pharma

Associate Principal Scientist - Large Molecule Bioanalytical

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeIndianapolis, IN, USAIn-person

About the Job

Requirements

  • A master's degree in a science field, or an equivalent combination of education, training, and experience accepted in lieu of a degree.
  • At least 8 years of experience with a master's degree or an equivalent combination of education, training, and experience in a bioanalytical laboratory environment.
  • Experience with antibodies, antibody-drug conjugates, or oligonucleotide conjugates containing payloads such as ASOs, PMOs, or siRNA.
  • Experience with large-molecule bioanalytical techniques such as mass spectrometry, CE-SDS, SDS-PAGE, BCA, SEC-HPLC, and ultraviolet-visible spectroscopy.
  • Experience evaluating the stability, potency, efficacy, and purity of therapeutic candidates used in in vitro or in vivo studies.
  • Ability to independently manage multiple complex projects, priorities, and experimental deliverables.
  • Scientific writing, presentation, data interpretation, and client communication skills.
  • Ability to collaborate across departments and contribute to multidisciplinary scientific discussions.
  • Advanced proficiency with Microsoft Excel, including statistical analysis, as well as PowerPoint, Word, and instrument-supporting software.
  • Working knowledge of applicable laboratory regulatory requirements, standard operating procedures, and good documentation practices.
  • Leadership, mentoring, organization, interpersonal effectiveness, and time management skills.

Responsibilities

  • Serve as the primary investigator on client studies, conduct laboratory work, and communicate study progress and results.
  • Design and execute complex bioanalytical method development experiments.
  • Evaluate and implement new methods, technologies, and instrumentation for client programs.
  • Prepare technical reports, study proposals, and protocols, including documentation that may support Food and Drug Administration submissions.
  • Lead multiple complex technical projects and guide or mentor junior scientific staff.
  • Analyze and interpret experimental findings, including statistical analysis, in accordance with laboratory standards.
  • Maintain laboratory notebooks, equipment, and study documentation in compliance with applicable regulatory standards, standard operating procedures, and good documentation practices.
  • Collaborate across functions to deliver studies, deploy methods, and provide project updates to team leads and project managers.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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