2,194 Clinical Trial Monitoring jobs in the United States
Clinical Research Associate
Posted 4 days ago
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Job Description
+ Oakland, CA
+ Highland General Hospital
+ HGH Opioid Use Disorder Grant
+ Services As Needed / Per Diem - Day
+ Allied Health
+ $57.84/HR
+ Req #:
+ FTE:0.01
+ Posted:October 8, 2025
**Summary**
**SUMMARY:** Under direction of the Manager of Grants & Special Projects, the Clinical Research Associate coordinates all aspects of clinical trials within the assigned unit.at the Adult Immunology Clinic, Highland Campus. In consultation with providers and other clinical personnel, is responsible for selecting, implementing and monitoring clinical trials, educating, and when appropriate, enrolling patients into the various programs. Performs related duties as required.
**DUTIES & ESSENTIAL JOB FUNCTIONS:** NOTE:The following are the duties performed by employees in this classification. However, employees may perform other related duties at an equivalent level. Not all duties listed are necessarily performed by each individual in the classification.
CLINICAL TRIALS:Responsible for assisting in the selection and administration of appropriate clinical research trials by reviewing studies, adhering to federal regulations and ICH Guidelines, with an emphasis on good clinical practice and clinical Safety Data Management. Administers informed consent, enrollment of participants into clinical trials.
INSTITUTIONAL REVIEW BOARD (IRB):Acts as departmental representative at Institutional Review Board's Human Subject Committee meetings. Presents all new research projects to the committee. Modifies, renews and closes out all appropriate research projects. Reports all serious adverse events and protocol violations. Submits drug and/or device safety reports to the IRB.
REGULATORY:Organizes research team and meets as needed. Maintains current CVs and licenses for all study investigators. Updates regulatory binders for each research study. Provides central protocol and drug information to departments. Educates hospital personnel regarding protocols and screening requirements. Reports serious adverse events to study sponsor and FDA, when appropriate. Ensures compliance with all federal and state laws regarding research and confidentiality. In collaboration with nursing staff, assures that operations are in compliance with external guidelines, statutory and accreditation parameters including JCAHO, Title 22, HCFA, OSHA, and other laws/regulations
PRESENTATION AND PUBLICATIONS:Assists investigators in the preparation of manuscripts and the design of posters and oral presentations for annual conventions, conferences and trainings, when appropriate. Performs searches through existing medical literature.
ADMINISTRATIVE/FISCAL:Organizes research team (nurses, co-investigators) and meets with team, as needed. Maintains current CVs and licenses for all sub investigators and binders for each protocol. Acts as the point person for budgetary and administrative issues. When appropriate, prepares and negotiates study budget. Monitors and accounts for all study related income and expenses. Requests and administers patient compensation and petty cash. Provides scheduled accounting of research funds to department directors. Interacts with AHS staff in a professional and courteous manner. Supervises research personnel to ensure compliance with protocols. Obtains, interview, and directly supervise research department volunteers and medical students on research elective rotations.
**MINIMUM QUALIFICATIONS:**
Education:Bachelor's Degree (180 quarter units or 120 semester units) with major coursework in health and human sciences, biology or a field related to the work. (Additional experience as outlined below may be substituted for the education on a year-to-year basis.)
Minimum Experience:Possess experience and expertise in medical research. Experience and expertise can be gained by "hands-on experience" in a medical or scientific setting, as a graduate or medical student or other medically trained individual. Typically equal to the equivalent of two years of full-time experience as a Clinical Research Associate or equivalent level position at a public hospital, medical center or HMO.
Required Licenses/Certifications:BLS - Basic Life Support Certification issued by AHA-American Heart Association.
_PAY RANGE: $57.84/HR_
_The pay range for this position reflects the base pay scale for the role at Alameda Health System. Final compensation will be determined based on several factors, including but not limited to a candidate's experience, education, skills, licenses and certifications, departmental equity, applicable collective bargaining agreements, and the operational needs of the organization. Alameda Health System also offers eligible positions a generous comprehensive benefits program._
Alameda Health System is an equal opportunity employer and does not discriminate against any employee or applicant for employment based on race, color, religion, national origin, age, gender, sex, ancestry, citizenship status, mental or physical disability, genetic information, sexual orientation, veteran status, or military background.
Clinical Research Associate
Posted 31 days ago
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Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
**What you will be doing**
+ Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
+ Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
+ Collaborating with investigators and site staff to facilitate smooth study conduct.
+ Performing data review and resolution of queries to maintain high-quality clinical data.
+ Contributing to the preparation and review of study documentation, including protocols and clinical study reports
**Your profile**
+ Bachelor's degree in a scientific or healthcare-related field.
+ Minimum of 2 years of experience as a Clinical Research Associate.
+ In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
+ Strong organizational and communication skills, with attention to detail.
+ Ability to work independently and collaboratively in a fast-paced environment.
+ Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver's license
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Clinical Research Associate
Posted today
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As a CRA, you will be responsible for site selection, initiation, monitoring, and close-out visits. You will ensure that clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. Your duties will include verifying the accuracy and completeness of source documents and patient records, managing investigational product accountability, and ensuring regulatory compliance at clinical trial sites. You will serve as the primary point of contact for investigators and study coordinators, providing essential support and guidance. Identifying and resolving site issues promptly and effectively will be a critical part of your role. You will also be involved in the preparation of study documentation, regulatory submissions, and reporting. The ability to maintain clear and concise communication with internal teams, external partners, and regulatory authorities is paramount. Our client is committed to advancing healthcare through rigorous research, and your contribution as a CRA will be vital to bringing life-changing therapies to patients. This position requires a keen eye for detail, strong organizational skills, and a passion for scientific integrity. You will have the opportunity to work on diverse therapeutic areas and contribute to groundbreaking medical advancements.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or related field. A Master's degree or equivalent experience is a plus. Proven experience as a Clinical Research Associate, with a strong understanding of ICH-GCP guidelines and regulatory requirements, is essential. Experience in (Specify Therapeutic Area, e.g., Oncology, Cardiology) is highly desirable. Excellent written and verbal communication skills, strong interpersonal skills, and the ability to build rapport with site staff are required. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is also necessary. A willingness to travel to clinical trial sites, as required, is a prerequisite for this role. If you are a results-oriented professional with a commitment to quality and a desire to make a significant impact in the pharmaceutical industry, we encourage you to apply and join our innovative team in Huntsville.
Clinical Research Associate
Posted today
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Job Description
Clinical Research Associate
Posted 5 days ago
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Job Description
Clinical Research Associate
Posted 9 days ago
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Job Description
The CRA will play a critical role in the planning, execution, and monitoring of clinical trials, ensuring data integrity, patient safety, and adherence to regulatory guidelines. You will be responsible for site management, including site initiation, routine monitoring, and close-out activities. This involves conducting on-site and remote visits to assess study conduct, data accuracy, and protocol compliance. The ideal candidate will possess a strong understanding of Good Clinical Practice (GCP) and relevant regulatory requirements.
Responsibilities:
- Identify, evaluate, and select clinical trial sites.
- Conduct site initiation visits to train site staff on the protocol and study procedures.
- Perform routine monitoring visits (on-site and remote) to ensure data quality and integrity.
- Verify source documentation against case report forms (CRFs).
- Oversee study drug accountability and investigational product management.
- Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and other applicable guidelines.
- Manage communication between clinical trial sites, the sponsor, and other stakeholders.
- Resolve site issues and implement corrective and preventative actions (CAPAs).
- Prepare monitoring reports and follow up on action items.
- Facilitate site close-out visits and ensure all study-related documentation is archived.
Qualifications:
- Bachelor's degree in a life science, nursing, or a related field. Advanced degree preferred.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, GCP, and regulatory requirements (e.g., FDA, EMA).
- Experience with various therapeutic areas is a plus.
- Excellent written and verbal communication skills.
- Strong organizational and time management abilities.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Ability to travel to sites as required (estimated 30-50%).
Clinical Research Associate
Posted 11 days ago
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Job Description
Key Responsibilities:
- Plan, initiate, monitor, and close-out clinical trial sites.
- Ensure adherence to study protocols, Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines.
- Verify the accuracy, completeness, and integrity of clinical trial data.
- Conduct site visits (remote and on-site) to assess trial progress, patient safety, and data quality.
- Train site staff on study requirements, protocols, and data collection procedures.
- Manage communication between the sponsor and clinical trial sites.
- Resolve site-specific issues and implement corrective actions as needed.
- Prepare site monitoring reports and maintain detailed study documentation.
- Ensure compliance with regulatory requirements and ethical considerations.
- Assist in the selection and qualification of potential clinical trial sites.
- Liaise with investigators, study coordinators, and other site personnel.
- Contribute to the development of study-related documents, such as informed consent forms and case report forms.
Qualifications:
- Bachelor's degree in a life science, healthcare, or related field; advanced degree preferred.
- Minimum of 3-5 years of experience as a Clinical Research Associate or in a similar clinical research role.
- Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements.
- Experience with various clinical trial phases and therapeutic areas.
- Excellent organizational, time management, and problem-solving skills.
- Strong written and verbal communication skills.
- Ability to travel to clinical trial sites as required (estimated 30-50% travel).
- Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Detail-oriented with a commitment to data accuracy and integrity.
- Ability to work independently and collaboratively within a team.
This hybrid position offers a competitive salary, comprehensive benefits package, and the opportunity to contribute to groundbreaking pharmaceutical research.
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Clinical Research Associate
Posted 12 days ago
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Job Description
Key Responsibilities:
- Conduct site visits (initiation, monitoring, close-out) according to study plan and protocol.
- Ensure investigator sites comply with study protocols, GCP, and regulatory requirements.
- Monitor patient recruitment and retention efforts at assigned sites.
- Verify accuracy and completeness of clinical data through source document review.
- Train and support site staff on study procedures and data entry requirements.
- Identify and resolve site-level issues and escalate as necessary.
- Liaise between investigators, study coordinators, and the sponsor.
- Review and manage essential regulatory documents.
- Contribute to study progress reports and provide updates on site performance.
- Ensure timely reporting of adverse events and protocol deviations.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Strong understanding of medical terminology and disease processes.
- Excellent organizational, time management, and problem-solving skills.
- Proficiency in data verification and query resolution.
- Excellent written and verbal communication skills.
- Ability to travel to clinical sites as required.
- Demonstrated ability to work independently and manage multiple studies.
Clinical Research Associate
Posted 14 days ago
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Job Description
Responsibilities:
- Monitor clinical trial sites to ensure compliance with protocols, SOPs, and regulatory guidelines (FDA, ICH-GCP).
- Verify the accuracy and completeness of clinical data through source data verification.
- Ensure patient safety and rights are protected throughout the trial.
- Manage communication between clinical trial sites, investigators, and the sponsor.
- Train site personnel on study-related procedures and documentation.
- Oversee the initiation, conduct, and close-out of clinical trial sites.
- Prepare and submit essential study documents.
- Resolve site issues and discrepancies in a timely manner.
- Conduct site visits, including pre-study, initiation, monitoring, and close-out visits.
- Maintain accurate and organized site files.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Minimum of 3 years of experience as a Clinical Research Associate or in a similar clinical research role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements.
- Experience with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Excellent monitoring and site management skills.
- Strong communication, interpersonal, and organizational abilities.
- Ability to travel frequently to clinical trial sites.
- Detail-oriented with strong problem-solving skills.
- Proficiency in Microsoft Office Suite.
Clinical Research Associate
Posted 15 days ago
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Job Description
Your primary responsibilities will include identifying, selecting, and training study sites. You will perform source data verification, ensuring accurate and complete documentation. You will also be responsible for monitoring subject recruitment and retention, conducting close-out visits, and ensuring compliance with Good Clinical Practice (GCP) guidelines and regulatory requirements. Effective communication with investigators, site staff, and internal project teams is paramount. You will manage communication channels, conduct remote monitoring activities, and address any site-specific issues or challenges promptly. Maintaining accurate and up-to-date trial documentation in electronic systems will be a core function.
The ideal candidate will possess a Bachelor's degree in a life science, nursing, or a related field. A minimum of 3-5 years of experience as a CRA or in a similar clinical research role is required. Strong knowledge of GCP, ICH guidelines, and relevant regulatory frameworks is essential. Excellent understanding of clinical trial processes and documentation is a must. Proficiency with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is expected. Exceptional organizational skills, strong analytical abilities, and the capacity to work independently and manage time effectively in a remote setting are critical. Outstanding written and verbal communication skills are necessary for interacting with diverse stakeholders. If you are a motivated and experienced CRA looking for a challenging remote opportunity within the pharmaceutical industry, we encourage you to apply.