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clinical trial coordinator

Biopharma Informatic

<div>
 
 Job Description:
 
 
 Biopharma Informatic is seeking an experienced Spanish-speaking Clinical Research Coordinator (CRC) with phlebotomy experience to join our team. This is a fully onsite role and is open only to candidates who are local to the area.
 
 
 
 
 
 We are specifically seeking candidates with hands-on Clinical Research Coordinator experience within physician office or private practice clinical trial settings. Experience obtained exclusively in hospital or university-based research environments does not fully align with the workflows, pace, and operational structure of this role.
 
 
 
 
 
 Required Spanish Fluency - Important Notice:
 
 
 Due to the needs of our patient population and the communication demands of this role, Spanish fluency is a strict requirement. Candidates must be able to communicate professionally and fully consent patients in Spanish without assistance. If you are not fully fluent in Spanish, please do not apply for this position.
 
 
 
 
 
 If you are not a Spanish speaker but are interested in joining Biopharma Informatic, we encourage you to explore and apply to any of our other open positions that align with your background. Please submit your application anytime through our careers portal: 🔗 https://www.biopharmainfo.net/careers
 
 
 
 
 
 Key Responsibilities:
 
 <ul>
 <li>
 Lead the coordination and execution of clinical trials across all phases: start-up, enrollment, maintenance, and close-out.
 </li>
 <li>
 Ensure proper receipt, handling, and accountability of investigational product (IP).
 </li>
 <li>
 Conduct and document the informed consent process in compliance with protocols and regulations.
 </li>
 <li>
 Serve as a liaison between physicians, study sponsors, and internal team members.
 </li>
 <li>
 Achieve or exceed study enrollment targets at assigned sites.
 </li>
 <li>
 Complete accurate and timely data entry in electronic data capture systems.
 </li>
 <li>
 Resolve data queries promptly to support project timelines and database lock.
 </li>
 <li>
 Maintain compliance with GCP, company SOPs, and industry regulations.
 </li>
 </ul>
 
 
 
 
 Qualifications:
 
 <ul>
 <li>
 2&ndash;5 years of Clinical Research Coordinator experience in a physician practice or private research setting.
 </li>
 <li>
 Spanish Fluency - must be able to consent patient without translator
 </li>
 <li>
 Phlebotomy experience is required
 </li>
 <li>
 Strong understanding of investigational product (IP) receipt, handling, and accountability.
 </li>
 <li>
 Proven experience conducting the informed consent process experience preferred
 </li>
 <li>
 Demonstrated ability to independently coordinate and manage clinical trials.
 </li>
 <li>
 Excellent organizational, communication, and problem-solving skills.
 </li>
 <li>
 Must be local to the area (onsite only; no relocation or remote work).
 </li>
 </ul>
 
 
 
</div>

Clinical Research Coordinator

Orange County Neuropsychiatric Rese

<div><div><div>NRC Research Institute has been conducting clinical trials for pharmaceutical and biotech companies since 2004. We specialize in pharmaceutical clinical trials involving Central Nervous System disorders such as Schizophrenia, Bipolar Disorder, Depression, ADHD, Autism and numerous medical indications in Rheumatology and Vaccine development. We are looking for an energetic and experienced Clinical Research Coordinator (CRC) to join our team at our Los Angeles location. 
</div><div>The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments. 
</div>
<div> 
Job Duties: 
</div><ul><li>Perform study procedures in accordance with GCP and study protocols</li><li>Coordinate protocol related research procedures, study visits, and follow-up care</li><li>Organize and maintain paper and electronic study data in a complete and correct manner</li><li>Work closely with recruitment and prescreening teams to meet study enrollment goals</li><li>Adhere to an IRB approved protocol</li><li>Participate in the informed consent process of study subjects</li><li>Support the safety of clinical research patients/research participants</li><li>Maintain study source documents</li><li>Report adverse events</li><li>Educate subjects and family on the protocol, study intervention, study drug, etc.</li><li>Comply with Institutional policies, standard operating procedures (SOPs) and guidelines</li><li>Complete case report forms (paper &amp; electronic data capture) and address queries</li><li>Facilitate study initiation, monitoring visits, and close out activities</li><li>Retain records/archive documents after study close out</li><li>Requires effective writing and communication, work as part of a team, ability to multitask</li><li>Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals</li><li>Document investigational product (drug/device) accountability</li></ul> 
<div>
 
Qualifications: 
</div><ul><li>Minimum five year of comprehensive pharmaceutical clinical research coordinator experience</li><li>Bachelor&rsquo;s Degree and/or healthcare licensure/certification required; degree in Biology and/or Psychology field preferred</li><li>Must be willing and able to work in a clinical setting involving a psychiatric/mentally disabled population</li><li>Must have ability to read and understand clinical trial protocols</li><li>Must have attention to detail and the ability to handle multiple tasks with precision</li><li>Must be adept with computers</li><li>Must possess excellent critical thinking skill</li><li>Must have excellent interpersonal and communication skills and be a hardworking team player</li><li>Must possess strong data management skills</li><li>Familiarity with medical terminology/environment required</li></ul> 
<div>
 
Compensation: 
</div><div>DOE 
Health, dental, and vision insurance, 401(k), and other benefits are available for eligible full-time employees. 
This is a full-time onsite position (40 hrs/week). Hours are Mon-Fri, 8:00 am - 4:30 pm</div></div></div><div></div>

Clinical Research Coordinator - Experienced

<div><div><div>NRC Research Institute has been conducting clinical trials for the world&rsquo;s pharmaceutical firms since 2004. We specialize in pharmaceutical clinical trials involving CNS (Central Nervous System) disorders such as Schizophrenia, Bipolar Disorder, Depression, ADHD, Autism, and more. We are looking for an energetic entry-level Clinical Research Coordinator (CRC) to join our team. 
</div><div>The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Principal Investigator and Scientific Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring a high level of knowledge of study specific protocols, as well as coordination and collaboration with research colleagues and departments. 
</div>
<div> 
Job Duties: 
</div><ul><li>Perform study procedures in accordance with GCP and study protocols</li><li>Coordinate protocol related research procedures, study visits, and follow-up care</li><li>Organize and maintain paper and electronic study data in a complete and correct manner</li><li>Work closely with recruitment and prescreening teams to meet study enrollment goals</li><li>Adhere to an IRB approved protocol</li><li>Participate in the informed consent process of study subjects</li><li>Support the safety of clinical research patients/research participants</li><li>Maintain study source documents</li><li>Report adverse events</li><li>Educate subjects and family on the protocol, study intervention, study drug, etc.</li><li>Comply with Institutional policies, standard operating procedures (SOPs) and guidelines</li><li>Complete case report forms (paper &amp; electronic data capture) and address queries</li><li>Facilitate study initiation, monitoring visits, and close out activities</li><li>Retain records/archive documents after study close out</li><li>Requires effective writing and communication, work as part of a team, ability to multitask</li><li>Act as liaison for research subject, investigator, IRB, sponsor, and healthcare professionals</li><li>Document investigational product (drug/device) accountability</li></ul>
<div>
 
Qualifications: 
 
<ul><li>Bachelor&rsquo;s Degree required; degree in Biology and/or Psychology field preferred</li><li>Must be willing and able to work in a clinical setting involving a psychiatric/mentally disabled population</li><li>Must have ability to read and understand clinical trial protocols</li><li>Must have attention to detail and the ability to handle multiple tasks with precision</li><li>Must be adept with computers</li><li>Must possess excellent critical thinking skill</li><li>Must have excellent interpersonal and communication skills and be a hardworking team player</li><li>Must possess strong data management skills</li><li>Familiarity with medical terminology/environment</li></ul></div> 
<div>
 
Compensation: 
Health, dental, and vision insurance, 401(k), and other benefits are available for eligible full-time employees. 
This is a full-time onsite position (40 hrs/week). Hours are Mon-Fri, 8:00 am - 4:30 pm</div></div></div>

Clinical Research Coordinator - Entry-Level

Cedars-Sinai

<div>
 
 Job Description
 
 
 
 
 Join Cedars-Sinai and become part of a team that is at the forefront of medical advancements!
 
 
 
 Work alongside physician-scientists and researchers who are making life-saving medical and scientific breakthroughs. Our team of scientists develop some of the most advanced clinical trials in the world. Ranked among the best in the nation by U.S. News &amp; World Report, our neurosurgeons and neurologists work together with experienced care teams to give patients the most effective treatment possible.
 
 
 
 About The Role
 
 
 
 This position will support the research programs in Department of Anesthesia and Neurology.
 
 
 The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The CRC I member is responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. This role is responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. The incumbent presents study information at research staff meeting. This position ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board.
 
 
 
 Primary Duties and Responsibilities:
 
 
 
 <ul>
 <li>
 Scheduling of research participants for research visits and procedures.
 </li>
 <li>
 In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) information about changes in research participant condition, adverse events, concomitant medication use, protocol compliance, and response to study drug.
 </li>
 <li>
 Schedules and participates in monitoring and auditing activities.
 </li>
 <li>
 Notifies direct supervisor about concerns regarding data quality and study conduct.
 </li>
 <li>
 Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters following local and federal guidelines.
 </li>
 <li>
 May perform other regulatory/Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.
 </li>
 <li>
 Maintains research practices using Good Clinical Practice (GCP) guidelines.
 </li>
 <li>
 Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
 </li>
 <li>
 Participates in required training and education programs.
 </li>
 <li>
 Coordinates training and education of other personnel.
 
 
 </li>
 </ul>
 
 Department-Specific Duties and Responsibilities:
 
 
 
 <ul>
 <li>
 Transportation of research medications.
 </li>
 <li>
 Performs research study related assessments and questionnaires.
 </li>
 <li>
 Assists with prescreening of research participants for various clinical trials.
 </li>
 <li>
 Attends research meetings and monthly conference calls with sponsors for study updates.
 </li>
 <li>
 Maintains organized paper and electronic research files.
 </li>
 <li>
 Performs all data collection and data entry tasks for department clinical trials.
 </li>
 <li>
 Assists with preparing manuscripts, letters, and other research documents as needed.
 </li>
 <li>
 Responds to sponsor&rsquo; inquiries regarding protocol start-up activities and recruitment.
 </li>
 <li>
 Performs literature reviews.
 
 
 </li>
 </ul>
 
 
 
 Qualifications
 
 
 
 
 
 
 Education:
 
 
 
 <ul>
 <li>
 High School Diploma/GED, required.
 </li>
 <li>
 Bachelor's degree in a Science, Sociology, or related field is preferred.
 
 
 </li>
 </ul>
 
 Licenses/Certifications:
 
 
 
 <ul>
 <li>
 ACRP/SOCRA certification is preferred.
 
 
 </li>
 </ul>
 
 Experience:
 
 
 
 <ul>
 <li>
 1 year of clinical research experience, required.
 
 
 </li>
 </ul>
 
 Overtime Status:
 
 NONEXEMPT
 
 
 
 Shift Length:
 
 8 hour
 
 
 
 Salary Range:
 
 $24 - $39.76
 
 
 
 Department:
 
 Research - Neurology
</div>

Clinical Research Coordinator I - Department of Neurology (Hybrid)

<div>
 
 Job Description
 
 
 
 
 Grow your career at Cedars-Sinai!
 
 
 
 The Angeles Clinic &amp; Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer!
 
 
 
 Join our team and contribute to groundbreaking research.
 
 
 
 We are seeking a dedicated Clinical Research Coordinator II to join our team. The ideal candidate will have a minimum of an Associate Degree or College Diploma and at least 3 years of clinical research coordination or related experience. A current Basic Life Support (BLS) Certification from the American Heart Association (AHA) &ndash; Healthcare Provider type &ndash; is required. Those with prior experience in oncology research are strongly encouraged to apply.
 
 
 The Clinical Research Coordinator II serves as the lead coordinator on an assigned portfolio of research studies, functioning independently to establish and coordinate logistics and processes for the conduct of research for the department. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all applicable regulatory requirements.
 
 
 <ul>
 <li>
 Establishes and completes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
 </li>
 <li>
 Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures and labs and completion and maintenance of consent forms, case report forms, SAE&rsquo;s and source documents.
 </li>
 <li>
 Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and supporting the informed consent process.
 </li>
 <li>
 Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution of queries from sponsors or regulatory entities.
 </li>
 <li>
 Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions.
 </li>
 <li>
 Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
 </li>
 <li>
 Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
 </li>
 <li>
 Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality.
 </li>
 <li>
 Plans and coordinates strategies for growing research participant enrollment, and/or improving clinical research efficiency as needed.
 </li>
 <li>
 Provides technical support for the preparation of grant proposals, publications, presentations and special projects.
 </li>
 <li>
 Provides assistance with research project budget development, including identifying and classifying routine care vs. research related care and provides assistance with research participant research billing and reconciliation.
 </li>
 <li>
 Participate in meetings and conferences related to research activities, including research staff meetings.
 </li>
 <li>
 Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as vital or requested; Participates in training and education of new research personnel.
 
 
 </li>
 </ul>
 
 
 
 Qualifications
 
 
 
 
 
 
 Educational Requirements:
 
 
 
 <ul>
 <li>
 Associates Degree/College Diploma required
 </li>
 <li>
 Bachelor's Degree preferred
 
 
 </li>
 </ul>
 
 Licenses/Certification:
 
 
 
 <ul>
 <li>
 Basic Life Support Certification (BLS) needs to be the AHA Healthcare Provider Type, required.
 </li>
 <li>
 SoCRA or ACRP certification preferred
 
 
 </li>
 </ul>
 
 Experience:
 
 
 
 <ul>
 <li>
 3 years of clinical research coordination or related experience.
 
 
 </li>
 </ul>
 
 Overtime Status:
 
 EXEMPT
 
 
 
 Shift Length:
 
 8 hour
 
 
 
 Salary Range:
 
 $31.46 - $48.76
 
 
 
 Department:
 
 Angeles Research Inst
</div>

Clinical Research Coordinator II - The Angeles Clinic & Research Institute

Flourish Research

<div>
 
 Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives!
 
 We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
 
 
 
 We are actively hiring Clinical Research Assistants at the Century City/Panorama City site locations. This is one of our three oncology research sites in the Greater Los Angeles area. These locations are formerly Valkyrie Clinical Trials - we are proud to welcome Valkyrie Clinical Trials to the Flourish Research network!
 
 
 
 The Clinical Research Assistant supports clinical research studies under the supervision of the Site Director or Clinical Research Coordinator. This role assists with clinic operations and study procedures across all phases of research, ensuring accurate data collection and compliance with GCP, IRB, and sponsor protocols
 
 while providing an impeccable patient experience in every, single interaction.
 
 
 
 
 Shift:
 
 Monday-Friday, 8:30 AM - 5 PM (occasional weekends)
 
 
 
 Location:
 
 2080 Century Pk E Suite 803, Los Angeles, CA 90067
 
 
 
 Compensation:
 
 $20 - $32/hr, depending on experience
 
 
 
 Benefits:
 
 Health, dental, and vision insurance plans, 401(k) with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Support CRCs and site staff with protocol-specified patient visits and procedures, which may include, but not limited to, phlebotomy, IVs, injections, vital signs, ECG/EKG, etc.
 </li>
 <li>
 Document assessments and study data per regs/GCP
 </li>
 <li>
 Obtain and document informed consent following federal regulations and IRB guidelines
 </li>
 <li>
 Support patient recruitment efforts and scheduling to meet enrollment goals
 </li>
 <li>
 Maintain accurate source documentation and complete case report forms (CRFs)
 </li>
 <li>
 Report adverse events to supervisors or investigators as needed
 </li>
 <li>
 Help manage study supplies, lab kits, and other trial materials
 </li>
 <li>
 Maintain confidentiality and follow all applicable compliance and ethical standards
 </li>
 <li>
 Communicate effectively with research team members and document relevant study communications
 </li>
 <li>
 Represent Flourish Research professionally in all interactions
 </li>
 <li>
 Perform additional duties as assigned by management
 
 
 </li>
 </ul>
 
 QUALIFICATIONS
 
 
 
 <ul>
 <li>
 Bachelor's degree preferred, but not required
 </li>
 <li>
 Oncology clinical research experience preferred
 </li>
 <li>
 Minimum of two years of clinical research experience
 </li>
 <li>
 Clinical skills preferred: vital signs, EKG/ECG, phlebotomy, and injections
 </li>
 <li>
 Familiar with e-source reporting via an electronic platform
 </li>
 <li>
 A clear understanding of ICH, FDA, and GCP regulations
 </li>
 <li>
 Impeccable organizational skills and attention to detail
 </li>
 <li>
 Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources
 </li>
 <li>
 An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven
 </li>
 <li>
 High-level critical thinking skills
 </li>
 <li>
 Working knowledge of medical terminology and lab collection/processing/storage procedures
 </li>
 <li>
 Proficiency with computers and Microsoft Office Suite
 
 
 </li>
 </ul>
 Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!
 
 
 
 Flourish Research is where clinical trials thrive.
 
 
 
 Flourish Research represents one of the industry's most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal, CNS, pulmonology, and vaccines.
 
 
 At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality.
 
 
 Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect.
 
 
 Flourish Research strives to build an organization that attracts and leverages diversity in our staff, which reflects the diversity of our local communities. We promote education, acceptance, and inclusion because there is beauty in diversity. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
 
 
 
 
 Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex, (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees.
 
 
</div>

Clinical Research Assistant

ICON Strategic Solutions

<div>
 Clinical Research Associate - Oncology (Start Up) - Los Angeles, CA
 
 
 ICON plc is a world-leading healthcare intelligence and clinical research organization. We&rsquo;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.
 
 
 
 What will you be doing?
 
 
 
 <ul>
 <li>
 Works on multiple trials within the Cross Therapeutic areas - Start up focus
 </li>
 <li>
 Collaborate with country operations teams to identify, select, and activate clinical trial sites in accordance with project timelines and requirements.
 </li>
 <li>
 Perform Site Qualification Visits (SQVs) to assess the eligibility of sites for participation in specific clinical studies.
 </li>
 <li>
 Build strong relationships with site personnel to facilitate a smooth onboarding process.
 </li>
 <li>
 Ensure that all activities adhere to ICH-GCP guidelines, local regulatory standards, and internal Standard Operating Procedures (SOPs).
 </li>
 <li>
 Coordinate with the country operations team to collect essential documents (such as regulatory approvals and contracts) to enable timely site activation.
 </li>
 <li>
 Act as the main point of contact for sites, study teams, and external stakeholders throughout the start-up process.
 </li>
 <li>
 Work closely with the country operations team to manage investigator contracts, regulatory documents, and site-specific start-up activities.
 </li>
 <li>
 Provide regular status updates to both internal and external stakeholders, ensuring alignment with important project milestones.
 </li>
 <li>
 Monitor, report on, and analyze key performance indicators (KPIs) related to site selection and start-up timelines.
 </li>
 <li>
 Proactively identify and address any issues that may delay study initiation or affect trial deliverables.
 </li>
 <li>
 Maintain precise documentation to ensure readiness for inspections.
 </li>
 <li>
 Support sites during the activation phase until they achieve &ldquo;Green Light&rdquo; status for site opening.
 </li>
 <li>
 Facilitate coordination with site staff to ensure all pre-study requirements, including contracts, budgets, and essential documentation, are met.
 </li>
 <li>
 Possibly assist in audit and inspection preparations to guarantee compliance with regulatory and ethical standards.
 
 
 </li>
 </ul>
 
 What do you need to have?
 
 
 
 <ul>
 <li>
 Have a minimum of a B.S., R.N., or equivalent degree, preferably in Biological Sciences
 </li>
 <li>
 Must be located in the Los Angeles area; near a major airport.
 </li>
 <li>
 Must have 2 -3 years&rsquo; experience in monitoring pharmaceutical industry clinical trials
 </li>
 <li>
 Have a minimum of 1-3 years' experience specifically monitoring oncology clinical trials
 </li>
 <li>
 Analytical/risk-based monitoring experience is an asset
 </li>
 <li>
 Ability to actively drive patient recruitment strategies at assigned sites
 </li>
 <li>
 Ability to partner closely with investigator and site staff to meet all of our study timelines
 </li>
 <li>
 Ability to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards/metrics, IWRS, safety reporting).
 </li>
 <li>
 Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face. Strong team member and self-starter with the ability to work independently.
 </li>
 <li>
 Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.
 </li>
 <li>
 To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status.
 
 
 </li>
 </ul>
 
 What ICON Can Offer You
 
 
 
 Our success depends on the quality of our people. That&rsquo;s why we&rsquo;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
 
 
 
 <ul>
 <li>
 Various annual leave entitlements
 </li>
 <li>
 A range of health insurance offerings to suit you and your family&rsquo;s needs.
 </li>
 <li>
 Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
 </li>
 <li>
 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&rsquo;s well-being.
 </li>
 <li>
 Life assurance
 </li>
 <li>
 Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
 
 
 </li>
 </ul>
 Visit our careers site to read more about the benefits ICON offers.
 
 
 At ICON, inclusion &amp; belonging are fundamental to our culture and values. We&rsquo;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
 
 
 Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless &ndash; there&rsquo;s every chance you&rsquo;re exactly what we&rsquo;re looking for here at ICON whether it is for this or other roles.
 
 
 Salary range: $91,336.00-$114,170.00
 
 
 
 Bonus, Com, Stock, Benefits &amp; Disclaimer Verbiage
 
 
 
 Actual compensation will be determined based on factors such as geographic location, work experience, education/training, and skill level. You may be eligible for a bonus, stock compensation and commissions in some cases depending on your role and performance.
 
 
 Are you a current ICON Employee? Please click here to apply
</div>

Clinical Research Associate

Explore 155+ Clinical trial coordinator in Los Angeles this March. Find roles across top companies and apply now to boost your career.