Senior Clinical Research Associate

{
  "content_hash": "5aeca60e4578d2b0ab1e92f2a270496b7f30aa5a46e6a08a1367342433ec20d8",
  "source_hash": "682de8e6ffd281cf4a30e19895b0f9cbc7f1e8ed1d6f5067b27dde9ab7b73b72",
  "last_changed_at": "2026-06-09T10:43:28.147Z",
  "active_status": "active"
}

{
  "language": "en",
  "location": {
    "raw": "Remote, West Coast , United States",
    "city": null,
    "region": "West Coast",
    "country": "United States",
    "is_remote": true,
    "confidence": 0.8
  },
  "salary_max": null,
  "salary_min": null,
  "inferred_at": "2026-06-19T10:35:39.196Z",
  "launch_scope": {
    "reason": "english_us_canada",
    "included": true,
    "language": "en",
    "location": {
      "raw": "Remote, West Coast , United States",
      "city": null,
      "region": "West Coast",
      "country": "United States",
      "is_remote": true,
      "confidence": 0.8
    },
    "countries": [
      "United States"
    ]
  },
  "remote_policy": "remote",
  "salary_period": null,
  "workplace_type": "remote",
  "salary_currency": null
}

{}

{
  "id": "744000130795524",
  "ref": "https://api.smartrecruiters.com/v1/companies/psicro/postings/744000130795524",
  "name": "Senior Clinical Research Associate",
  "uuid": "408838d8-a762-4a72-8901-075227e081f3",
  "detail": {
    "id": "744000130795524",
    "name": "Senior Clinical Research Associate",
    "uuid": "408838d8-a762-4a72-8901-075227e081f3",
    "jobAd": {
      "sections": {
        "jobDescription": {
          "text": "<p>As a Senior Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.&#xa0; You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance.</p><p>You will:</p><ul><li>Conduct and report all types of onsite monitoring visits</li><li>Be involved in study startup (if applicable)</li><li>Perform CRF review, source document verification and query resolution</li><li>Be responsible for site communication and management</li><li>Supervise study activities, timelines, and schedules on the country level</li><li>Be a point of contact for in-house support services and vendors</li><li>Be involved in quality control, such as compliance monitoring and reports review</li><li>Participate in feasibility research</li><li>Support regulatory team in preparing documents for study submissions</li></ul>",
          "title": "Job Description"
        },
        "qualifications": {
          "text": "<ul><li>College/University degree in Life Sciences or an equivalent combination of education, training &amp; experience</li><li>Independent on-site monitoring experience in the USA (5 years minimum)</li><li>Experience in all types of monitoring visits in Phase I-III</li><li>Participation in clinical projects as a Senior Monitor</li><li>Experience monitoring complex Oncology&#xa0;trials required; experience with radiopharmaceuticals and/or breast cancer preferred</li><li>Experience monitoring GI studies (IBD, Chron's, UC) is preferred.&#xa0;</li><li>Full working proficiency in English</li><li>Proficiency in MS Office applications</li><li>Ability to plan, multitask and work in a dynamic team environment</li><li>Communication, collaboration, and problem-solving skills</li><li>Ability to travel up to 80%</li><li>Valid driver’s license (if applicable)</li></ul><p><strong><em>For this position PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.</em></strong></p>",
          "title": "Qualifications"
        },
        "companyDescription": {
          "text": "<p>We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.&#xa0; A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals.&#xa0; We work on the front-line of medical science, changing lives, and bringing new medicines to those who need them.</p><p>If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.</p>",
          "title": "Company Description"
        },
        "additionalInformation": {
          "text": "<p>Advance your career in clinical research and lead challenging full-service projects on the country/regional level&#xa0;while growing with a rapid&#xa0;company, that puts its people first! You will get hands-on involvement in every aspect of the study.</p><p>For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.</p>",
          "title": "Additional Information"
        }
      }
    },
    "jobId": "d441f288-36d4-40a8-8b9f-ccd3ffea44f2",
    "active": true,
    "company": {
      "name": "PSI CRO",
      "identifier": "PSICRO"
    },
    "creator": {
      "name": "Lauren Pettrey",
      "avatarUrl": "https://c.smartrecruiters.com/sr-employee-image-prod-aws-dc5/6149d4e560c60977dc080677?r=s3-eu-central-1&_1636747975368"
    },
    "jobAdId": "627ce83b-c915-48e0-a18b-71198b916a36",
    "applyUrl": "https://jobs.smartrecruiters.com/PSICRO/744000130795524-senior-clinical-research-associate?oga=true",
    "function": {
      "id": "quality_assurance",
      "label": "Quality Assurance"
    },
    "industry": {
      "id": "pharmaceuticals",
      "label": "Pharmaceuticals"
    },
    "language": {
      "code": "en",
      "label": "English",
      "labelNative": "English (US)"
    },
    "location": {
      "city": "Remote",
      "hybrid": false,
      "region": "West Coast ",
      "remote": true,
      "country": "us",
      "fullLocation": "Remote, West Coast , United States"
    },
    "refNumber": "REF3010P",
    "department": {
      "id": 1063561,
      "label": "Clinical"
    },
    "postingUrl": "https://jobs.smartrecruiters.com/PSICRO/744000130795524-senior-clinical-research-associate",
    "visibility": "PUBLIC",
    "customField": [
      {
        "fieldId": "COUNTRY",
        "valueId": "us",
        "fieldLabel": "Country/Region",
        "valueLabel": "United States"
      },
      {
        "fieldId": "5b615e106d8bc52f977e9866",
        "fieldLabel": "Job Summary",
        "valueLabel": "As a Senior CRA you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance."
      },
      {
        "fieldId": "5a8ea76ab60a5e06821bfc7b",
        "valueId": "default",
        "fieldLabel": "Brands",
        "valueLabel": "PSI CRO"
      },
      {
        "fieldId": "5a8ea76ab60a5e06821bfc7c",
        "valueId": "1063561",
        "fieldLabel": "Department",
        "valueLabel": "Clinical"
      }
    ],
    "referralUrl": "https://jobs.smartrecruiters.com/external-referrals/company/PSICRO/publication/408838d8-a762-4a72-8901-075227e081f3?dcr_ci=PSICRO",
    "defaultJobAd": true,
    "releasedDate": "2026-06-08T13:03:54.454Z",
    "experienceLevel": {
      "id": "mid_senior_level",
      "label": "Mid-Senior Level"
    },
    "typeOfEmployment": {
      "id": "permanent",
      "label": "Full-time"
    }
  },
  "company": {
    "name": "PSI CRO",
    "identifier": "PSICRO"
  },
  "creator": {
    "name": "Lauren Pettrey"
  },
  "jobAdId": "627ce83b-c915-48e0-a18b-71198b916a36",
  "function": {
    "id": "quality_assurance",
    "label": "Quality Assurance"
  },
  "industry": {
    "id": "pharmaceuticals",
    "label": "Pharmaceuticals"
  },
  "language": {
    "code": "en",
    "label": "English",
    "labelNative": "English (US)"
  },
  "location": {
    "city": "Remote",
    "hybrid": false,
    "region": "West Coast ",
    "remote": true,
    "country": "us",
    "fullLocation": "Remote, West Coast , United States"
  },
  "refNumber": "REF3010P",
  "department": {
    "id": "1063561",
    "label": "Clinical"
  },
  "visibility": "PUBLIC",
  "customField": [
    {
      "fieldId": "COUNTRY",
      "valueId": "us",
      "fieldLabel": "Country/Region",
      "valueLabel": "United States"
    },
    {
      "fieldId": "5a8ea76ab60a5e06821bfc7b",
      "valueId": "default",
      "fieldLabel": "Brands",
      "valueLabel": "PSI CRO"
    },
    {
      "fieldId": "5a8ea76ab60a5e06821bfc7c",
      "valueId": "1063561",
      "fieldLabel": "Department",
      "valueLabel": "Clinical"
    },
    {
      "fieldId": "5b615e106d8bc52f977e9866",
      "fieldLabel": "Job Summary",
      "valueLabel": "As a Senior CRA you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance."
    }
  ],
  "defaultJobAd": true,
  "releasedDate": "2026-06-08T13:03:54.454Z",
  "detail_errors": [],
  "experienceLevel": {
    "id": "mid_senior_level",
    "label": "Mid-Senior Level"
  },
  "typeOfEmployment": {
    "id": "permanent",
    "label": "Full-time"
  }
}