Senior Research Associate

2 weeks ago


San Mateo, California, United States ATR International Full time
Job Overview

Position Title: Senior Research Associate

Employment Type: Contract - 12 Months

Work Arrangement: Hybrid (3 days onsite, 2 days remote)

Compensation: $38.00/hr

ATR International is in search of a dedicated Senior Research Associate for a prominent client.

Key Responsibilities:

  • Act as the coordinator for high-throughput early discovery assays, adhering to established work protocols.
  • Collaborate effectively with internal research teams and multi-site Contract Research Organizations (CROs) to ensure timely receipt and upload of data and reports into databases, aiding project teams in assessing safety risks.
  • Conduct quality control reviews of nonclinical regulatory documents, data tables, study protocols, and reports.
  • Assist with administrative duties, including document management as needed.

Qualifications and Skills:

  • Minimum of 2 years of experience in the pharmaceutical or CRO sector, specifically in small molecule and/or biopharmaceutical drug development.
  • Exceptional attention to detail and commitment to quality.
  • Proficient in managing multiple tasks, with strong planning skills to meet deadlines.
  • Strong computer proficiency, particularly in Microsoft Word, PowerPoint, and Excel.
  • Bachelor's or Associate's degree in a relevant scientific field.

Experience Requirements:

At least 1 year of experience in the pharmaceutical or CRO industry focusing on small molecule and/or biopharmaceutical drug development.

Essential Skills:

  • Experience in the pharmaceutical or CRO industry, particularly with small molecule and/or biopharmaceutical drug development.
  • Ability to prioritize tasks and plan effectively to meet deadlines.
  • Strong skills in Microsoft Office Suite, including Word, PowerPoint, and Excel.

Preferred Skills:

  • Advanced degree (BS or MS) in a related scientific discipline with 3+ (MS) or 5+ (BS) years of relevant experience.
  • Understanding of the fundamental principles and methodologies in toxicology, as well as knowledge of animal and human biology and physiology.

Unique Aspects of This Role: This position offers valuable experience within a company that values scientific advancement and patient care, fostering an environment that promotes innovation, diversity, and the personal and professional growth of its employees. Gain extensive knowledge as a Study Monitor for nonclinical toxicology studies conducted at CROs, overseeing the technical and scientific execution of studies.

Required Education: Bachelor's or Associate's degree in a scientific discipline.

Benefits Include:

  • MEC/ACP Medical Coverage
  • Optional Dental, Vision, Life, and Supplemental Income Plans
  • 401k Plan (subject to eligibility requirements)
  • Sick Leave as mandated by state or county regulations


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