Associate Scientist II

Location : Location US-MD-Rockville
ID 2024-4631
Research and Science
Full Time - Permanent


Associate Scientist


Corporate Responsibilities:

  • Adherence to laboratory health and safety procedures
  • Adherence to Standard Operating Procedures (SOPs)
  • Adherence to applicable company policies and guidelines
  • Adherence to federal and/or local regulations as applicable

 Essential Position Responsibilities: 

  • Be responsible for sample preparation and running batches for bioanalytical method development (PK, ADA, biomarkers, DNA, RNA, genomics, flow), validation and sample analysis in support of preclinical and clinical drug development under the supervision of the scientists.
  • Collaborate with the scientists to develop innovative bioanalytical techniques in support of contemporary therapeutic strategies discovered by Inotiv’s client base.
  • Ensure compliance is maintained, continuing Inotiv’s phenomenal track record of successful FDA audits.
  • Assist with performing method development, validation, sample analysis, solve issues, and failures with internal and external project teams in a collaborative and supportive manner.
  • Assist in the creation, maintenance, and improvement of standardized tools for method development and validation activities; identify opportunities for automation to increase speed and efficiency.
  • Identify new approaches, methodology, and/or the advent of state-of-the-art equipment


  • Self-driven, creative, and entrepreneurial by being resourceful, optimistic, fiscally responsible, innovative, fearless, determined, open-minded, and focused.
  • Balanced and dynamic communication style that radiates honesty, integrity, and credibility through effective use of active listening skills and follow through.
  • Superior relationship-building skills with all levels of internal and external stakeholders and clients.
  • Compelled to join highly desirable and sought-after employer that that will drive their development toward their aspirations.
  • Naturally inquisitive and adept at crafting lines of questions that reveal deep and complete insights into situations and challenges.
  • Self-assured and confident, yet humble and open-minded; place the team ahead of personal interests and ambitions.
  • Solutions-oriented personality that embraces challenges as opportunities and demonstrates a persistent drive to take initiative and diplomatically resolve issues or challenges.
  • Strong sense of personal accountability and responsibility; propels throughout the organization.
  • Assertive and driven to exceed expectations in a way that inspires others to do the same.
  • Exceptional attention to detail and quality; strong organizational capabilities.

Working Conditions & Physical Requirements

  • Ability to push, pull, lift 20 pounds unassisted.
  • Stand / walk for extended period of time.
  • Sit and work at a computer for extended period of time.
  • Fine manipulation including handle touch object or tools and ability to handled controls to perform work.
  • Ability to read and interpret materials, verbally communicate, and hear required. 


  • BSc or MSc in Immunology, molecular biology, bioanalytical chemistry, drug metabolism, pharmacokinetics, or related science, with 1-3 years of bioanalytical experience in the pharmaceutical industry, biotech field or a drug discovery & development or clinical CRO.
  • Experience in quantitative analysis of biological samples (e.g. blood, plasma, urine, tissue, etc.) for exogenous (mainly drugs) and endogenous compounds for Biotherapeutics and Biomarker compounds preferred.
  • Preferably good knowledge and practical experience with the requirements of ISO and Good Laboratory Practice (GLP) or other laboratory accreditation systems standards.
  • Experience in running batches for method development and validation of large molecules for PK, ADA and NAb using ELISA, MSD, Luminex, PCR and cell-based assays for e.g., proteins, peptides, monoclonal antibodies, oligonucleotides, cell and gene therapy products and other biomarker analysis including flow analysis preferable.
  • Experience interfacing with supervising scientists on a wide range of bioanalytical method development projects.

Additional Requirements:

  • Demonstrated expertise in bioanalytical chemistry best practices and processes.
  • Understanding of GLP/GCP/GMP/GCLP regulations; ability to apply practices daily.
  • Excellent written and verbal communication skills (English required); open, interactive style that facilitates high levels of trust.
  • Exceptional project management and organizational skills.
  • Exceptional partnering and collaboration skills with stakeholders at all levels.
  • Superior interpersonal skills that demonstrate high levels of emotional intelligence and critical thinking.
  • Self-starter, capable of working independently to generate desired results.
  • Proficiency with MS Office Suite products.

*This position could be offered at different levels for candidates who qualify with a combination of advanced levels of education and/or years of experience.  The salary range will adjust along with the level of the role to match the person’s relevant experience and/or education level.


Inotiv is a growing contemporary drug discovery and development company where we “Play to Win” in an industry rich with opportunity.  Together, we face challenges and together we win in the delivery of world-class drug discovery and development solutions that impact the health and well-being of people all over the world.  There’s an opportunity for everyone at all phases of a career, each individual’s unique skill set has an impact on the work we conduct. If you have the talent and desire to impact the quality of people’s lives, we have the career opportunities to make it happen.  Join us in embracing research and science to impact the health and well-being of people all over the world.


Inotiv has been named a 2023 Top Workplace!

Salary will be commensurate with experience and responsibilities. Benefits include health and dental coverage, short- and long-term disability, paid time off, paid parental leave, 401K, and more!


Inotiv is an Equal Opportunity Employer. It is our policy to provide a fair and equal employment opportunity to all persons, regardless of age, race, color, religion, sex, gender, gender identity, gender expression, sexual orientation, genetic information, disability, national origin, veteran status, or any other basis prohibited by law. This policy governs all aspects of employment, including selection, job assignment, compensation, discipline, termination and access to benefits and training.




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