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• AB

  Clinical Research Associate II

  AbbVie

  Pay not stated · This website uses cookies. By continuing to use this site, you are giving your consent to cookies being used. See our Privacy policy for more info. <iframe src="https://www.googletagmanager.com/ns.html?id=GTM-53KLF8" height="0" width="0" style="display:none;visibility:hidden"></iframe> JUMP TO CONTENT Life at AbbVie english English Español Français 中文(中国) 中文(台灣) Deutsch Italiano 日本語 Nederlands Polski Türkçe Русский Français Canadien Português (Brazil) 0 Save 0 [id="4f9aad77-262b-ac19-ee33-f72a1e1aed01"]:not(.custom-styled) .banner-customhtml { background-size: cover; height: 285px; width: 100%; } Clinical Research Associate II __jobinformationwidget.freetext.LocationText__ Beijing, Beijing Function: Research & Development document.body.className += " function-researchdevelopment"; Work location type: Hybrid document.body.className += " worklocationtype-hybrid"; document.body.className += " "; Job Type: Full-time document.body.className += " jobtype-fulltime"; document.body.className += " "; Job ID: R00153089 Apply Save Company DescriptionAbout AbbVieAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.Job DescriptionList up to 10 main responsibilities for the job. Include information about the accountability and scope."Considered as the Pprimary Sponsor pPoint of contact for the investigative site. Advanced level of competency or experience in providing contextual information on the clinical trials, connecting stakeholders to the investigative sites and strengthening Abbvie's positioning. Ability to motivate and align monitoring community through leadership and mentorship."Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership. Able to support, guide, and mentor junior personnel on Site Management activities."Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects.Superior understanding of site engagement and ability to customize site engagement strategy for assigned study/ies and critically apply new strategies as needed. Gather local/site insights and utilize site engagement tools to report/track progress and measure impact of that strategy.Superior level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Expert understanding to generate and ensure effective recruitment and retention techniques/plans based on the patient disease journey. Develop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance."Possesses advanced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development. Supports local onboarding of more junior CRAs. Demonstrates ability to openly listen to and consider viewpoints to enhance outcomes.May participate/lead in global/local task forces and initiatives. Responsible for activities as assigned by manager. "Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues. Superior ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution. Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a custIndependently Identifies, evaluates and recommends new/potential investigators/sites on an on going basis demonstrating expert understanding and decision making. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Ensures audit and regulatory inspection readiness at assigned clinical site at all times. Manages investigator payments as per executed contract obligations, as applicable.QualificationsAppropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific, Pharmacy, Nursing) preferred.Minimum of 3 years of clinically related experience, of which a period of 2 years is preferable in independent clinical research monitoring of investigational drug or device trials in any therapeutic area. Familiar with risk‐based monitoring approach, onsite and offsite monitoring.Knowledge of appropriate therapeutic area indications with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trialsSuperior knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.Demonstrate advanced communication skills and superior cross-functional collaboration skills among internal and external stakeholders.Demonstrate superior planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.Superior ability to leverage technology, tools and resources to provide customer centric support based on the health of the site.Superior interpersonal skills with excellent written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training.Ability to independently use functional expertise, leverage critical thinking skills and apply good judgement to address clinical site issuesActs with integrity in accordance with AbbVie code of business conduct and leadership values. Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.Additional InformationAbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.htmlUS & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:https://www.abbvie.com/join-us/reasonable-accommodations.html {"@context":"http://schema.org","@type":"JobPosting","url":"https://careers.abbvie.com/en/job/clinical-research-associate-ii-in-beijing-beijing-jid-35573","title":"Clinical Research Associate II ","description":"<br/><div class='jobad-companydescription'>Company Description</div><br/><p><strong>About AbbVie</strong></p><p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at <a href=\"http://www.abbvie.com/\" rel=\"noopener noreferrer\">www.abbvie.com</a>. Follow @abbvie on <a href=\"https://www.linkedin.com/company/abbvie/\" rel=\"noopener noreferrer\">LinkedIn,</a> <a href=\"https://www.facebook.com/AbbVieGlobal/\" rel=\"noopener noreferrer\">Facebook</a>, <a href=\"https://www.instagram.com/abbvie/\" rel=\"noopener noreferrer\">Instagram</a>, <a href=\"https://twitter.com/abbvie\" rel=\"noopener noreferrer\">X</a> and <a href=\"https://www.youtube.com/user/AbbVie\" rel=\"noopener noreferrer\">YouTube.</a></p><br/><div class='jobad-jobdescription'>Job Description</div><br/><p>List up to 10 main responsibilities for the job. Include information about the accountability and scope.</p><ul><li>\"Considered as the Pprimary Sponsor pPoint of contact for the investigative site. Advanced level of competency or experience in providing contextual information on the clinical trials, connecting stakeholders to the investigative sites and strengthening Abbvie's positioning.<br>\nAbility to motivate and align monitoring community through leadership and mentorship.\"</li><li>Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership. Able to support, guide, and mentor junior personnel on Site Management activities.</li><li>\"Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects.</li><li>Superior understanding of site engagement and ability to customize site engagement strategy for assigned study/ies and critically apply new strategies as needed. Gather local/site insights and utilize site engagement tools to report/track progress and measure impact of that strategy.</li><li>Superior level of competency connecting the study protocol, scientific principles and clinical trial requirements to the day-to-day clinical trial execution activities. Expert understanding to generate and ensure effective recruitment and retention techniques/plans based on the patient disease journey.<br>\nDevelop solid knowledge of therapeutic area, asset and clinical landscape / patient journey to enable successful patient recruitment and overall protocol compliance.\"</li><li>Possesses advanced level of competency to mentor and train less experienced CRAs on various aspects of work and provides input into their development. Supports local onboarding of more junior CRAs. Demonstrates ability to openly listen to and consider viewpoints to enhance outcomes.</li><li>May participate/lead in global/local task forces and initiatives. Responsible for activities as assigned by manager.<br>\n\"</li><li>Responsible for continuous risk-assessment proactively, and in collaboration with Central Monitoring team, monitor activities conducted by clinical sites to detect early overall study performance or patient safety issues. Superior ability to think critically to resolve site risk signals while having robust understanding of site processes to drive study execution. Ensures preventative and corrective action plans are put into place, as needed, to mitigate risk and promote compliance using a cust</li><li>Independently Identifies, evaluates and recommends new/potential investigators/sites on an on going basis demonstrating expert understanding and decision making. Potential sites may be identified through networking or internal AbbVie requests to assist in the placement of planned clinical studies with qualified investigators.</li><li>Ensures quality of data submitted from study sites and assures timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. Ensures audit and regulatory inspection readiness at assigned clinical site at all times. Manages investigator payments as per executed contract obligations, as applicable.</li></ul><br/><div class='jobad-qualifications'>Qualifications</div><br/><ul><li>Appropriate tertiary qualification in health related disciplines (e.g., Medical, Scientific, Pharmacy, Nursing) preferred.</li><li>Minimum of 3 years of clinically related experience, of which a period of 2 years is preferable in independent clinical research monitoring of investigational drug or device trials in any therapeutic area. Familiar with risk‐based monitoring approach, onsite and offsite monitoring.</li><li>Knowledge of appropriate therapeutic area indications with the ability to understand and apply scientific concepts as they relate to the conduct of clinical trials</li><li>Superior knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.</li><li>Demonstrate advanced communication skills and superior cross-functional collaboration skills among internal and external stakeholders.</li><li>Demonstrate superior planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines.</li><li>Superior ability to leverage technology, tools and resources to provide customer centric support based on the health of the site.</li><li>Superior interpersonal skills with excellent written, verbal, active listening and presentation skills, with ability to establish and leverage site relationships and trusted partnerships through engagement, motivation, and training.</li><li>Ability to independently use functional expertise, leverage critical thinking skills and apply good judgement to address clinical site issues</li><li>Acts with integrity in accordance with AbbVie code of business conduct and leadership values. Self-motivated individual focused on delivering timely and quality outcomes in a fast-paced environment.</li></ul><br/><div class='jobad-additionalInformation'>Additional Information</div><br/><div sr-tagline=\"\"></div><p>AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. </p><p>US & Puerto Rico only - to learn more, visit <a href=\"https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html\" rel=\"noopener noreferrer\">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html</a></p><p>US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:</p><p><a href=\"https://www.abbvie.com/join-us/reasonable-accommodations.html\" rel=\"noopener noreferrer\">https://www.abbvie.com/join-us/reasonable-accommodations.html</a></p>","datePosted":"2026-11-09T04:01:16+00:00","validThrough":"2126-11-09T04:01:16+00:00","employmentType":["Full-time"],"hiringOrganization":{"@type":"Organization","name":"AbbVie","image":"","logo":"","sameAs":"https://careers.abbvie.com/en","url":"https://careers.abbvie.com/en"},"industry":["Research & Development"],"jobBenefits":"","identifier":{"@type":"PropertyValue","name":"AbbVie","value":"f076e763-9aa1-4510-83fc-495566c704d8"},"jobLocation":[{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Beijing, Beijing"}}]} Recruitment Fraud Alert We have recently become aware of various recruitment phishing scams targeting job seekers. Please be advised: AbbVie will never request sensitive personal information (such as bank account details, social security numbers, or payment of any kind) during the recruitment process. If you suspect you have received a fraudulent offer or communication claiming to be from AbbVie, please do not respond, open any attachments, or click on any hyperlinks. If you have any questions or concerns regarding the authenticity of a communication alleged to have been made by or on behalf of AbbVie, please contact us immediately. Protect yourself by verifying job offers and communications. Your safety is important to us. document.body.className += " "; Where We Work Role is primarily site- or office-based but can occasionally be performed remotely. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role. 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  AuditingClinical ResearchDirect Patient CareGene EditingMolecular Biology +8

  3+ yrs exp 22 hours ago

  More Apply
• 

  Clinical Research Associate

  Icon

  Pay not stated · Chicago, IL

  Regulatory RequirementsPatient Safety

  Entry level 5 days ago

  More Apply
• 

  Clinical Research Associate 2

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  Pay not stated · Chicago, IL

  Data IntegrityPatient SafetyRegulations

  Entry level · 2+ yrs exp 1 week ago

  More Apply
• 

  CRA II

  Icon

  Pay not stated · US, Downers Grove, IL

  Data IntegrityPatient SafetyRegulationsICH Guidelines

  Entry level · 2+ yrs exp 1 week ago

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• 

  Senior CRA - Phase I Oncology Chicago or Milwaukie

  Icon

  Pay not stated · US, Blue Bell (ICON)

  Data IntegrityGood Clinical PracticeQuality ControlRegulatory RequirementsClinical Research +2

  1 week ago

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• 

  Clinical Research Associate II

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  Pay not stated · Chicago, IL

  Clinical ResearchData EntryClinical Systems

  Mid level · 2+ yrs exp 3 weeks ago

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• PA

  Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available

  Patheon

  Pay not stated · Chicago, Illinois, United States of America

  Mid level 2 weeks ago

  Apply
• 

  Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available

  Thermo Fisher Scientific

  Pay not stated · Chicago, Illinois, United States of America

  Mid level 2 weeks ago

  Apply