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Scientist, In Vivo Pharmacology

Terray Therapeutics, Inc. · Remote (United States), United States · Remote · Active · $120,000–$175,000 / year · Rippling ATS

Job facts

FieldValue
CompanyTerray Therapeutics, Inc.
TitleScientist, In Vivo Pharmacology
Normalized title-
Department / teamTranslational Biology
LocationUnited States
Work modelRemote / Remote
Employment typeFull Time
Salary$120,000–$175,000 / year
Statusactive
ATS providerRippling ATS
Posted / first seen2026-05-29 / 2026-05-30
Changed / last seen2026-06-18 / 2026-06-18

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Department jobsActive postings in Translational Biology.Open
Work model jobsActive Remote postings.Open
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Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyTerray Therapeutics, Inc.
Sourceb638d6a5-a25f-4ad1-8912-4978ed56454d
ATS providerRippling ATS

Description

company Company Overview: Terray Therapeutics is a venture-backed biotechnology company where scientists and engineers build together to transform how small-molecule drugs are discovered and developed. By combining our nanotechnology, experimental science, machine learning, and automation, we leverage Terray’s ability to generate and learn from scale proprietary chemical data to discover novel medicines for patients in need. At Terray, you will work alongside pioneers and experts in artificial intelligence, chemistry, drug discovery, automation, and nanotechnology in deeply interconnected workflows where computational and experimental teams continuously learn from one another. Our platform, EMMI (Experimentation Meets Machine Intelligence), powers iterative cycles of molecular design and wet-lab experimentation that rapidly improve our understanding of biochemical interactions and guide the next generation of discoveries. Our teams support both an internal immunology pipeline and partnerships across a broad range of therapeutic areas. The work here is highly collaborative, fast-moving, and grounded in the belief that breakthroughs happen when strong science, thoughtful technology, and great people work closely together. role Position Summary: Terray Therapeutics is seeking a highly motivated and experienced in vivo scientist with expertise in models of autoimmunity and inflammation to join our Translational Biology team. In this role, the candidate will serve as a scientific and operational lead for outsourced in vivo pharmacology and nonclinical safety/toxicology studies, with responsibilities including study design, execution and monitoring, vendor oversight, project management and cross-functional coordination. The position will report to the Director of Translational Biology. The core responsibilities of this position are: Provide scientific leadership and oversight for in vivo pharmacology studies focused on inflammation, autoimmunity, or related therapeutic areas in support of advancing our pipeline programs As the pharmacology representative, collaborate cross-functionally with preclinical teams, project leads, and external consultants to advance our pipeline programs through in vivo studies Lead and monitor outsourced in vivo pharmacology and nonclinical safety/toxicity studies conducted at CROs, ensuring scientific rigor, protocol compliance, data quality, and timely execution Contribute to study design, protocol development and review, endpoint selection and data interpretation Review study reports, datasets and summaries to ensure scientific accuracy and completeness Coordinate study timelines, logistics, milestones, budgets and deliverables across multiple external vendors and internal stakeholders Manage CRO relationships, including vendor selection, performance oversight, issue resolution and communication Maintain study documentation, ensuring compliance with regulatory requirements and company policies Present study updates and recommendations to project teams and leads Support contract management activities (scopes of work, purchase orders, invoice tracking) Experience and Qualifications: Part of Terray's success is nurtured by a hands-on work environment where everyone is accountable, vested in a vision of excellence, and actively taking part in the success of the business. Terray supports a positive work environment where employees can feel engaged, recognized, and empowered to be creative. Required Qualifications: Ph.D. degree in biology, immunology, pharmacology, toxicology, or a related field 3+ years of experience in biotech or pharmaceutical industry supporting nonclinical drug development programs Strong scientific background in inflammation, immunology, or immune-related diseases Extensive experience with rodent in vivo pharmacology and translational disease models Strong scientific data analysis, interpretation, and problem-solving skills Strong understanding of nonclinical drug development workflow Experience managing or monitoring outsourced studies at CROs Demonstrated project management and organizational skills with the ability to manage multiple studies and priorities simultaneously Excellent written, verbal, and presentation skills Ability to work effectively in cross-functional teams and to thrive in a highly collaborative research environment Preferred Qualifications: Experience with vendor oversight, contract management, and budget tracking Experience supporting IND-enabling and preclinical development programs Knowledge of GLP and non-GLP study conduct and non-clinical assessment Familiarity with IACUC regulations and animal welfare standards Compensation Details: $ 120,000 – $175,000 annually, depending on experience. Terray’s salary ranges are designed to be competitive and are benchmarked against market base salary plus bonus within our industry and market. We align pay to role scope, skill level, and impact. We invest heavily in benefits because taking care of our people matters. Our programs are benchmarked at the top of the Southern California market and designed to provide meaningful support across every stage of life. Benefits include participation in the Company’s stock option plan, a 3% retirement safe harbor contribution, fully paid health, dental, vision insurance for our employees, spouse, partner and families as well as above-market life insurance, disability coverage, and much more to explore during the offer process.

Full job record

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Source IDb638d6a5-a25f-4ad1-8912-4978ed56454d
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Providerrippling
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TitleScientist, In Vivo Pharmacology
Normalized Title—
Statusactive
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Location TextRemote (United States), United States
DepartmentTranslational Biology
Team—
Employment Typefull_time
Workplace Typeremote
Remote Policyremote
CountryUnited States
Region—
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Salary RawCompensation Details: $ 120,000 – $175,000 annually, depending on experience
Salary Min120,000
Salary Max175,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://ats.rippling.com/terraytx/jobs/56b8cea8-c116-4b44-8bf4-aca8fccf02c0
Apply URLhttps://ats.rippling.com/terraytx/jobs/56b8cea8-c116-4b44-8bf4-aca8fccf02c0
First Seen At2026-05-30 07:42:40Z
Last Seen At2026-06-18 09:30:19Z
Last Checked At2026-06-18 09:30:19Z
Last Changed At2026-06-18 09:30:19Z
Inactive At—
Source Posted At2026-05-29 22:33:31Z
Source Updated At—
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      "role": "<meta><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><b><strong style=\"font-size:11pt;white-space:pre-wrap;\">Position Summary:&nbsp;</strong></b><span style=\"font-size:11pt;white-space:pre-wrap;\">Terray Therapeutics is seeking a highly motivated and experienced in vivo scientist with expertise in models of autoimmunity and inflammation to join our Translational Biology team. In this role, the candidate will serve as a scientific and operational lead for outsourced in vivo pharmacology and nonclinical safety/toxicology studies, with responsibilities including study design, execution and monitoring, vendor oversight, project management and cross-functional coordination. The position will report to the Director of Translational Biology.</span></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">The core responsibilities of this position are:&nbsp;</span></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Provide scientific leadership and oversight for in vivo pharmacology studies focused on inflammation, autoimmunity, or related therapeutic areas in support of advancing our pipeline programs</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">As the pharmacology representative, collaborate cross-functionally with preclinical teams, project leads, and external consultants to advance our pipeline programs through in vivo studies </span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Lead and monitor outsourced in vivo pharmacology and nonclinical safety/toxicity studies conducted at CROs, ensuring scientific rigor, protocol compliance, data quality, and timely execution</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Contribute to study design, protocol development and review, endpoint selection and data interpretation</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Review study reports, datasets and summaries to ensure scientific accuracy and completeness</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Coordinate study timelines, logistics, milestones, budgets and deliverables across multiple external vendors and internal stakeholders</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Manage CRO relationships, including vendor selection, performance oversight, issue resolution and communication</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Maintain study documentation, ensuring compliance with regulatory requirements and company policies</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Present study updates and recommendations to project teams and leads</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Support contract management activities (scopes of work, purchase orders, invoice tracking)</span></li></ul><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><br></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;\"><b><strong style=\"font-size:11pt;white-space:pre-wrap;\">Experience and Qualifications:&nbsp;</strong></b><span style=\"font-size:11pt;white-space:pre-wrap;\">Part of Terray's success is nurtured by a hands-on work environment where everyone is accountable, vested in a vision of excellence, and actively taking part in the success of the business.  Terray supports a positive work environment where employees can feel engaged, recognized, and empowered to be creative.</span></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;\"><i><em style=\"font-size:11pt;white-space:pre-wrap;\">Required Qualifications:</em></i><span style=\"font-size:11pt;white-space:pre-wrap;\">&nbsp;</span></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Ph.D. degree in biology, immunology, pharmacology, toxicology, or a related field</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">3+ years of experience in biotech or pharmaceutical industry supporting nonclinical drug development programs </span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Strong scientific background in inflammation, immunology, or immune-related diseases</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Extensive experience with rodent in vivo pharmacology and translational disease models</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Strong scientific data analysis, interpretation, and problem-solving skills</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Strong understanding of nonclinical drug development workflow</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Experience managing or monitoring outsourced studies at CROs</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Demonstrated project management and organizational skills with the ability to manage multiple studies and priorities simultaneously</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Excellent written, verbal, and presentation skills</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"color:black;white-space:pre-wrap;\">Ability to work effectively in cross-functional teams and to thrive in a highly collaborative research environment</span></li></ul><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;\"><i><em style=\"font-size:11pt;white-space:pre-wrap;\">Preferred Qualifications:</em></i></p><ul data-pattern=\"discCircleSquare\" data-depth=\"1\" style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;margin:8px 0px;line-height:1.6;padding:0px 0px 0px 32px;list-style-type:disc;\"><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Experience with vendor oversight, contract management, and budget tracking</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Experience supporting IND-enabling and preclinical development programs</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Knowledge of GLP and non-GLP study conduct and non-clinical assessment</span></li><li style=\"font-size:11pt;margin:3px 0px;letter-spacing:0.25px;line-height:1.6;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Familiarity with IACUC regulations and animal welfare standards</span></li></ul><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;\"><br></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;\"><b><strong style=\"font-size:11pt;white-space:pre-wrap;\">Compensation Details:</strong></b><span style=\"font-size:11pt;white-space:pre-wrap;\">&nbsp;$</span><span style=\"white-space:pre-wrap;\">120,000 </span><span style=\"font-size:11pt;white-space:pre-wrap;\">– $175,000 annually, depending on experience. Terray’s salary ranges are designed to be competitive and are benchmarked against market base salary plus bonus within our industry and market. We align pay to role scope, skill level, and impact. </span></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;\"><br></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:left;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">We invest heavily in benefits because taking care of our people matters. Our programs are benchmarked at the top of the Southern California market and designed to provide meaningful support across every stage of life. Benefits include participation in the Company’s stock option plan, a 3% retirement safe harbor contribution, fully paid health, dental, vision insurance for our employees, spouse, partner and families as well as above-market life insurance, disability coverage, and much more to explore during the offer process.  </span></p>",
      "company": "<meta><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><b><strong style=\"font-size:11pt;white-space:pre-wrap;\">Company Overview:</strong></b><span style=\"font-size:11pt;white-space:pre-wrap;\"> Terray Therapeutics is a venture-backed biotechnology company where scientists and engineers build together to transform how small-molecule drugs are discovered and developed. By combining our nanotechnology, experimental science, machine learning, and automation, we leverage Terray’s ability to generate and learn from scale proprietary chemical data to discover novel medicines for patients in need.  </span></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><br></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">At Terray, you will work alongside pioneers and experts in artificial intelligence, chemistry, drug discovery, automation, and nanotechnology in deeply interconnected workflows where computational and experimental teams continuously learn from one another. Our platform, EMMI (Experimentation Meets Machine Intelligence), powers iterative cycles of molecular design and wet-lab experimentation that rapidly improve our understanding of biochemical interactions and guide the next generation of discoveries. </span></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:12pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;\"><br></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><span style=\"font-size:11pt;white-space:pre-wrap;\">Our teams support both an internal immunology pipeline and partnerships across a broad range of therapeutic areas. The work here is highly collaborative, fast-moving, and grounded in the belief that breakthroughs happen when strong science, thoughtful technology, and great people work closely together. </span></p><p style=\"font-family:&quot;Basel Grotesk&quot;,Arial,sans-serif;font-size:11pt;font-weight:400;line-height:1.6;letter-spacing:0.25px;margin:4px 0px;padding:0px;text-align:justify;\"><br></p>"
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          "title": "Phone number",
          "required": true,
          "fieldType": "PHONE_NUMBER"
        },
        {
          "oid": "location",
          "title": "Location (city only)",
          "required": true,
          "fieldType": "SHORT_ANSWER"
        },
        {
          "oid": "resume",
          "title": "Resume",
          "required": true,
          "fieldType": "FILE"
        },
        {
          "oid": "cover_letter",
          "title": "Cover letter",
          "required": false,
          "fieldType": "FILE"
        }
      ],
      "customQuestions": {
        "fields": [
          {
            "oid": "first_name",
            "title": "First name",
            "required": true,
            "fieldData": {},
            "fieldType": "SHORT_ANSWER"
          },
          {
            "oid": "last_name",
            "title": "Last name",
            "required": true,
            "fieldData": {},
            "fieldType": "SHORT_ANSWER"
          },
          {
            "oid": "email",
            "title": "Email",
            "required": true,
            "fieldData": {},
            "fieldType": "SHORT_ANSWER"
          },
          {
            "oid": "pronouns",
            "title": "Pronouns",
            "required": false,
            "fieldData": {},
            "fieldType": "PRONOUN"
          },
          {
            "oid": "current_company",
            "title": "Current company",
            "required": false,
            "fieldData": {},
            "fieldType": "SHORT_ANSWER"
          },
          {
            "oid": "phone_number",
            "title": "Phone number",
            "required": true,
            "fieldData": {},
            "fieldType": "PHONE_NUMBER"
          },
          {
            "oid": "location",
            "title": "Location (city only)",
            "required": true,
            "fieldData": {},
            "fieldType": "SHORT_ANSWER"
          },
          {
            "oid": "resume",
            "title": "Resume",
            "required": true,
            "fieldData": {},
            "fieldType": "FILE"
          },
          {
            "oid": "cover_letter",
            "title": "Cover letter",
            "required": false,
            "fieldData": {},
            "fieldType": "FILE"
          }
        ]
      },
      "additionalQuestions": null
    },
    "hasAIEvaluationsEnabled": false,
    "eeocQuestionnaireEnabled": true,
    "applicationConfirmationTemplate": "66e8834cf67d53328394edfd",
    "eeocQuestionnaireEnabledForJobPost": true
  },
  "detail_meta": {
    "url": "https://ats.rippling.com/api/v2/board/terraytx/jobs/56b8cea8-c116-4b44-8bf4-aca8fccf02c0",
    "http_status": 200,
    "content_type": "application/json",
    "response_bytes": 17273
  },
  "detail_errors": []
}
Get this page with API

Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/3b539102805165dc8be616c5d107a2f6c3674a47?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/d6d63b47-914b-4de4-b42d-13ef96638b8bJSON
GET https://api.bluedoor.sh/job-postings/v1/sources/b638d6a5-a25f-4ad1-8912-4978ed56454dJSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/3b539102805165dc8be616c5d107a2f6c3674a47/eventsJSON

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