Senior Research Associate, Pharmacology

Senior Research Associate, Pharmacology

As a member of the pharmacology group, we seek a scientifically curious and motivated individual with an ability to work in a fast-paced environment. The right candidate will develop and execute the bioanalytical method development to support pharmacokinetics (PK) sample analysis. This position is hands-on and requires the effective experiment execution, communication, and documentation of results that enable the advancement of novel research molecules toward development candidates. Strong candidates will be hard working, efficient, collaborative, and passionate about drug discovery and development. Experience in ligand binding assay development and routine sample analysis is desired. This position will report directly to the principal scientist of in vivo Pharmacology.

ESSENTIAL FUNCTIONS AND RESPONSIBILITIES

These may include, but are not limited to:

• Identify, develop and execute ligand binding assays and other in vitro assays to support both in vivo and in vitro pharmacology studies.

• Proven track record of ligand binding assay development and participation of routine preclinical and/or clinical sample analysis. Independently execute assays from assay development, qualification (if required), sample analysis, data analysis, report and SOP drafting (if required).

• Analyze and present experimental data using Prism, Excel, MS Office or similar software, and present findings to cross-functional groups.

• Produce detailed documentation of experiments within a lab notebook and electronically.

• Ability to schedule and prioritize workload effectively within a multi-task environment.

EDUCATION, EXPERIENCE, KNOWLEDGE, SKILLS AND ABILITIES

• Bachelor’s degree in biology, biochemistry, bioengineering, chemical biology, or related scientific discipline with 3-5+ years of experience in biotech/pharmaceutical industry, or Master’s degree with 2+ years of experience.

• Requires experience in ligand binding assay development, qualification/validation and sample analysis.

• Competence in data analysis tools (Excel, GraphPad). Candidates with experience in data management, coding and programming in Excel or other data management software would be a plus.

• Hands-on expertise with ELISA and MSD assays is required. Experience of flow cytometry and cell culture is a plus.

• Strong analytical and critical thinking skills with the ability to work in a fast-paced and collaborative environment.

• Excellent written and oral communication skills.

Compensation:

In addition to a competitive base salary ranging from $95,000 to $105,000, we offer stock options, a stock purchase plan (ESPP) and a target bonus. Janux also provides a comprehensive benefits package for our employees and their families, which includes medical, dental, vision, and supplemental disability insurance.

Please note that the base salary range is a guideline, and individual total compensation will vary based on factors such as qualifications, skill level, competencies, internal equity and work location.

Job Type: Full-time

Benefits:

• 401K

• Medical insurance

• Dental insurance

• Vision insurance

• Supplemental disability insurance plans

• Flexible schedule

• Life insurance

• Flexible vacation

• Sick time

• Incentive stock option plan

• Relocation assistance

Schedule:

• Monday to Friday

Work authorization:

• United States (Required)

Additional Compensation:

• Annual targeted bonus %

Work Location:

• On site (San Diego, CA)

EQUAL OPPORTUNITY EMPLOYER:

Janux Therapeutics, Inc. is an equal opportunity employer that is committed to providing a work environment free of harassment and discrimination based upon a protected category, as well as an environment free from retaliation for protected activity