Clinical Research Associate II

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  "detail": {
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    "heading": "Clinical Research Associate II",
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    "description_html": "<span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Title: Clinical Research Associate II</span></b></span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><i><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Location</span></span></i></b><i><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">: </span></span></i><i><span style=\"font-family:Roboto;\">This position is based in our Campbell, California offices. This position <u>is on-site, full-time + Travel Considerations.</u></span></i></span></span></span><br><br><span style=\"font-size:16px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">Why Imperative Care?</span></span></span></b></span></span></span><br><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Do you want to make a real impact on patients? Imperative Care is changing the way stroke and vascular diseases are treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.</span></span></span></span></span><br><br><span style=\"font-size:16px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Do</span></span></span></b></span></span></span><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"> </span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Provide in-house clinical operations support by assisting with study documentation, site coordination, and day-to-day clinical trial activities to help ensure successful study execution.</span></span></span></span></span><ul><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Support the preparation, organization, and maintenance of essential clinical study documentation and study files</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Coordinate with clinical sites and internal teams to support ongoing study activities and communication</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Conduct clinical monitoring and data verification activities to ensure high-quality study execution and data integrity across trial site</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Review study documentation for completeness, accuracy, and compliance with company and regulatory standards</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Provide operational and administrative support to the clinical team in a fast-paced medical device environment</span></span></span></span></span></li></ul><span style=\"font-size:16px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Bring</span></span></span></b></span></span></span><ul><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Bachelor’s degree in life sciences or related field with 1–3 years of clinical research or medical device experience</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Basic understanding of FDA regulations, ICH-GCP guidelines, and clinical trial processes</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Strong organizational skills with high attention to detail and documentation accuracy</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Excellent communication and collaboration skills with the ability to manage multiple priorities</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Self-motivated, adaptable, and eager to grow within a clinical research and operations environment</span></span></span></span></span></li></ul><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Employee Benefits</span></span></b> <span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">include a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.</span></span></span></span><br><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">Salary Range: $101,000 - 106,000 annually</span></span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#202124;\">Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer. </span></span></span></span></span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Join Us! </span></b><a href=\"https://imperativecare.com/careers/\" style=\"color:#0000FF;text-decoration:underline;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Apply Today</span></span></b></a></span></span></span><br> <p>The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.</p>\n\n<p>Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.</p>",
    "description_text": "Title: Clinical Research Associate II\n Location : This position is based in our Campbell, California offices. This position is on-site, full-time + Travel Considerations.\n Why Imperative Care?\n Do you want to make a real impact on patients? Imperative Care is changing the way stroke and vascular diseases are treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.\n What You’ll Do\n Provide in-house clinical operations support by assisting with study documentation, site coordination, and day-to-day clinical trial activities to help ensure successful study execution. Support the preparation, organization, and maintenance of essential clinical study documentation and study files\n Coordinate with clinical sites and internal teams to support ongoing study activities and communication\n Conduct clinical monitoring and data verification activities to ensure high-quality study execution and data integrity across trial site\n Review study documentation for completeness, accuracy, and compliance with company and regulatory standards\n Provide operational and administrative support to the clinical team in a fast-paced medical device environment\n What You’ll Bring Bachelor’s degree in life sciences or related field with 1–3 years of clinical research or medical device experience\n Basic understanding of FDA regulations, ICH-GCP guidelines, and clinical trial processes\n Strong organizational skills with high attention to detail and documentation accuracy\n Excellent communication and collaboration skills with the ability to manage multiple priorities\n Self-motivated, adaptable, and eager to grow within a clinical research and operations environment\n Employee Benefits include a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.\n Salary Range: $101,000 - 106,000 annually\n Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer.\n Join Us! Apply Today\n  The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.\n Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.",
    "jsonld_jobposting": {
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      "title": "Clinical Research Associate II",
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      "datePosted": "2026-05-20",
      "description": "<span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Title: Clinical Research Associate II</span></b></span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><i><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Location</span></span></i></b><i><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">: </span></span></i><i><span style=\"font-family:Roboto;\">This position is based in our Campbell, California offices. This position <u>is on-site, full-time + Travel Considerations.</u></span></i></span></span></span><br><br><span style=\"font-size:16px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">Why Imperative Care?</span></span></span></b></span></span></span><br><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Do you want to make a real impact on patients? Imperative Care is changing the way stroke and vascular diseases are treated. As part of our team, you’d be developing breakthroughs that will revolutionize the future of stroke care. Every day, the technologies that we develop at Imperative Care directly impact human lives. Our focus is on the needs of the patient, and they come first in everything we do.</span></span></span></span></span><br><br><span style=\"font-size:16px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Do</span></span></span></b></span></span></span><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"> </span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Provide in-house clinical operations support by assisting with study documentation, site coordination, and day-to-day clinical trial activities to help ensure successful study execution.</span></span></span></span></span><ul><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Support the preparation, organization, and maintenance of essential clinical study documentation and study files</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Coordinate with clinical sites and internal teams to support ongoing study activities and communication</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Conduct clinical monitoring and data verification activities to ensure high-quality study execution and data integrity across trial site</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Review study documentation for completeness, accuracy, and compliance with company and regulatory standards</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Provide operational and administrative support to the clinical team in a fast-paced medical device environment</span></span></span></span></span></li></ul><span style=\"font-size:16px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#ed7d31;\">What You’ll Bring</span></span></span></b></span></span></span><ul><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Bachelor’s degree in life sciences or related field with 1–3 years of clinical research or medical device experience</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Basic understanding of FDA regulations, ICH-GCP guidelines, and clinical trial processes</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Strong organizational skills with high attention to detail and documentation accuracy</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Excellent communication and collaboration skills with the ability to manage multiple priorities</span></span></span></span></span></li><li style=\"margin-right:49px;\"><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">Self-motivated, adaptable, and eager to grow within a clinical research and operations environment</span></span></span></span></span></li></ul><span style=\"font-size:14px;\"><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Employee Benefits</span></span></b> <span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\">include a stake in our collective success with stock options, bonus, competitive salaries, a 401k plan, health benefits, generous PTO, and a parental leave program.</span></span></span></span><br><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"font-family:Roboto;\">Salary Range: $101,000 - 106,000 annually</span></span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><span style=\"background:#FFFFFF;\"><span style=\"line-height:115%;\"><span style=\"font-family:Roboto;\"><span style=\"color:#202124;\">Please note that the salary information is a general guideline only. Imperative Care considers factors such as scope and responsibilities of the position, candidate's work experience, education/training, key skills, and internal equity, as well as location, market and business considerations when extending an offer. </span></span></span></span></span></span><br><span style=\"line-height:115%;\"><span style=\"font-family:Calibri, sans-serif;\"><b><span style=\"font-family:Roboto;\">Join Us! </span></b><a href=\"https://imperativecare.com/careers/\" style=\"color:#0000FF;text-decoration:underline;\"><b><span style=\"font-family:Roboto;\"><span style=\"color:#ed8b00;\">Apply Today</span></span></b></a></span></span></span><br> <p>The use of external recruiters/staffing agencies requires prior approval from our Human Resources Department. The Human Resources Department at Imperative Care requests that external recruiters/staffing agencies not to contact Imperative Care employees directly in an attempt to present candidates. Complying with this request will be a factor in determining future professional relationships with Imperative Care.</p>\n\n<p>Imperative Care will not accept unsolicited resumes from any source other than candidates themselves for either current or future positions. Submission of unsolicited resumes in advance of an agreement between the Human Resources Department and the external recruiter/staffing agency does not create any implied obligation on the part of Imperative Care.</p>",
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