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senior clinical research associate

Thermo Fisher Scientific

<div>Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Fluctuating Temps hot/cold
Job Description
Join Us as a Senior Clinical Research Associate (Level I) &ndash; Make an Impact at the Forefront of Innovation 
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
 
 
As part of our global team, you&rsquo;ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix. 
 
What You&rsquo;ll Do: 
<ul><li>Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable</li><li>Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.</li><li>Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.</li><li>Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.</li><li>Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).</li><li>Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.</li><li>Responds to company, client and applicable regulatory requirements/audits/inspections.</li><li>Maintains &amp; completes administrative tasks such as expense reports and timesheets in a timely manner.</li><li>Contributes to other project work and initiatives for process improvement, as required.</li></ul> 
Education and Experience Requirements:
 
<ul><li>Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
</li><li>Valid driver's license where applicable</li><li>In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
</li></ul> 
Knowledge, Skills and Abilities:
 
<ul><li>Effective clinical monitoring skills</li><li>Demonstrated understanding of medical/therapeutic area knowledge and medical terminology</li><li>Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents</li><li>Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving</li><li>Ability to manages Risk Based Monitoring concepts and processes</li><li>Effective oral and written communication skills, with the ability to communicate effectively with medical personnel</li><li>Ability to maintain customer focus through the utilization of good listening skills, attention to detailand the ability to perceive customers&rsquo; underlying issues</li><li>Effective interpersonal skills</li><li>Strong attention to detail</li><li>Effective organizational and time management skills</li><li>Ability to remain flexible and adaptable in a wide range of scenarios</li><li>Ability to work in a team or independently as required</li><li>Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software</li><li>Good English language and grammar skills</li><li>Good presentation skills</li></ul> 
Working Conditions and Environment:
 
<ul><li>Working Conditions and Environment:</li><li>Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.</li><li>Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.</li><li>May also include extended overnight stays.</li><li>Exposure to biological fluids with potential exposure to infectious organisms.</li><li>Personal protective equipment required such as protective eyewear, garments and gloves.</li><li>Exposure to fluctuating and/or extreme temperatures on rare occasions.</li><li>Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.</li></ul></div>

Senior CRA

Cedars-Sinai Medical Center

<div><h2 class="jobSectionHeader">Job Description</h2>

The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and specialized care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.

Join our team and use your skill with an organization known nationally for excellence in research!

Job Summary:

The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. This role evaluates and abstracts research data and ensures compliance with protocol and research objectives. Position is responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. This role will comply with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.

Job Duties and Responsibilities:

Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.

Evaluates and abstracts clinical research data from source documents.

Ensures compliance with protocol and overall clinical research objectives.

Completes Case Report Forms (CRFs).

Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.

Provides supervised patient contact or patient contact for long term follow-up patients only.

Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.

Assists with clinical trial budgets and patient research billing as needed

Schedules patients for research visits and research procedures.

Responsible for sample preparation and shipping and maintenance of study supplies and kits.

Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.

Maintains research practices using Good Clinical Practice (GCP) guidelines.

Maintains strict patient confidentiality according to HIPAA regulations and applicable law.

Participates in required training and education programs. 

<h2 class="jobSectionHeader">Qualifications</h2>

Education:
High School diploma/GED required.
BA/BS degree in Science, Sociology or related degree preferred.
Experience:
Understanding of general research objectives.
1 year of clinical research related experience preferred.<ul><li>
Excellent language skills and understanding of Grants, Manuscript, and Abstract guidelines.</li><li>
Strong verbal and writing ability as well as communication, computer, organization, personnel and time-management skills.</li><li>
Proficiency in Word, PowerPoint and Excel.</li><li>
Ability to work independently, set priorities, and handle multiple tasks requiring attention to detail.</li><li>
Previous experience in research environment preferred.</li></ul>
Physical Demands:<ul><li>
Able to perform moderate lifting.</li><li>
Able to sit, stand and walk for prolonged periods of time</li><li>
Able to read papers and online documents.</li><li>
Able to operate standard office equipment</li><li>
Able to exercise physical ability and perspective acuity to satisfactorily perform essential job functions.</li></ul></div>

Heart Institute Clinical Research Associate I - Cheng Lab

TRIO - Translational Research in Oncology

<div>
 If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!
 
 
 Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.
 
 
 TRIO is looking for a CRA to join our Monitoring Resources team in the USA. This position will be remote, based out of the West Coast, and will require travel.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects
 </li>
 <li>
 Conduct Pre-Study Site Visits (or calls), Study Initiation Visits, Routine Monitoring Visits and Site Close-out at assigned clinical study sites as per TRIO SOPs/SGs/IMs and study- specific SGs/IMs
 </li>
 <li>
 Perform source document verification, validate Case Report Forms (CRFs) and perform query resolution in a timely manner to ensure clean data availability for studies analyses
 </li>
 <li>
 Input and maintain study information in tracking systems: Provide regular/accurate sites status updates and common site trends to Monitoring Resources and Project Management Departments
 </li>
 <li>
 Oversee study drug management at clinical study sites (availability, receipt, handling, storage, dispensation, tracking and accountability, and destruction/return)
 </li>
 <li>
 Perform Investigator Study File reconciliation: request any new or updated site-related essential documents and review them for content, consistency with other documents, and compliance with local regulatory requirements, ICH-GCPs guidelines, SOPs
 </li>
 <li>
 Respond to requests from clinical study sites in a timely fashion
 </li>
 <li>
 Establish and maintain good rapport with clinical study sites
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 At least 2 years of oncology experience as CRA, Coordinator, and/or research nurse.
 </li>
 <li>
 Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health Science &ndash; or its international equivalent
 </li>
 <li>
 Local regulatory requirements knowledge would be a major asset
 </li>
 <li>
 At least one year of experience on an early phase trial
 </li>
 <li>
 Expereince with Breast, Lung, Gastric, and/or Ovarian Tumors would be a major asset
 </li>
 <li>
 Good knowledge of medical terminology and clinical monitoring process
 </li>
 <li>
 Strong ICH-GCPs knowledge
 </li>
 <li>
 Ability to prioritize multiple tasks and achieve project timelines
 </li>
 <li>
 Effective time management in order to meet daily metrics or team objectives
 </li>
 <li>
 Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail
 </li>
 <li>
 Ability to travel up to 60% on average
 
 
 </li>
 </ul>
 
 What TRIO Can Offer You
 
 
 
 <ul>
 <li>
 Competitive Salary
 </li>
 <li>
 3 weeks of vacation plus paid Christmas Closure
 </li>
 <li>
 2 weeks paid personal/sick time
 </li>
 <li>
 100% health benefits for you and your family paid by TRIO
 </li>
 <li>
 Flexible working hours
 </li>
 <li>
 Monthly internet allowance
 </li>
 <li>
 401K Program 5% Salary Contribution
 </li>
 <li>
 Home office allowance
 </li>
 <li>
 Luggage allowance
 
 
 </li>
 </ul>
 Pay Range: $112,000 - $146,000. Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.
</div>

Clinical Research Associate

Translational Research in Oncology

<div>
 If you are an experienced Clinical Research Associate who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you!
 
 
 Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.
 
 
 TRIO is looking for a CRA to join our Monitoring Resources team in the USA. This position will be remote, based out of the West Coast, and will require travel.
 
 
 
 Responsibilities
 
 
 
 <ul>
 <li>
 Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects
 </li>
 <li>
 Conduct Pre-Study Site Visits (or calls), Study Initiation Visits, Routine Monitoring Visits and Site Close-out at assigned clinical study sites as per TRIO SOPs/SGs/IMs and study- specific SGs/IMs
 </li>
 <li>
 Perform source document verification, validate Case Report Forms (CRFs) and perform query resolution in a timely manner to ensure clean data availability for studies analyses
 </li>
 <li>
 Input and maintain study information in tracking systems: Provide regular/accurate sites status updates and common site trends to Monitoring Resources and Project Management Departments
 </li>
 <li>
 Oversee study drug management at clinical study sites (availability, receipt, handling, storage, dispensation, tracking and accountability, and destruction/return)
 </li>
 <li>
 Perform Investigator Study File reconciliation: request any new or updated site-related essential documents and review them for content, consistency with other documents, and compliance with local regulatory requirements, ICH-GCPs guidelines, SOPs
 </li>
 <li>
 Respond to requests from clinical study sites in a timely fashion
 </li>
 <li>
 Establish and maintain good rapport with clinical study sites
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 At least 2 years of oncology experience as CRA, Coordinator, and/or research nurse.
 </li>
 <li>
 Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health Science &ndash; or its international equivalent
 </li>
 <li>
 Local regulatory requirements knowledge would be a major asset
 </li>
 <li>
 At least one year of experience on an early phase trial
 </li>
 <li>
 Expereince with Breast, Lung, Gastric, and/or Ovarian Tumors would be a major asset
 </li>
 <li>
 Good knowledge of medical terminology and clinical monitoring process
 </li>
 <li>
 Strong ICH-GCPs knowledge
 </li>
 <li>
 Ability to prioritize multiple tasks and achieve project timelines
 </li>
 <li>
 Effective time management in order to meet daily metrics or team objectives
 </li>
 <li>
 Experience using computerized information systems, electronic spreadsheets, word processing and electronic mail
 </li>
 <li>
 Ability to travel up to 60% on average
 
 
 </li>
 </ul>
 
 What TRIO Can Offer You
 
 
 
 <ul>
 <li>
 Competitive Salary
 </li>
 <li>
 3 weeks of vacation plus paid Christmas Closure
 </li>
 <li>
 2 weeks paid personal/sick time
 </li>
 <li>
 100% health benefits for you and your family paid by TRIO
 </li>
 <li>
 Flexible working hours
 </li>
 <li>
 Monthly internet allowance
 </li>
 <li>
 401K Program 5% Salary Contribution
 </li>
 <li>
 Home office allowance
 </li>
 <li>
 Luggage allowance
 
 
 </li>
 </ul>
 Pay Range: $112,000 - $146,000. Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data.
 
 
 Prior to applying please review TRIO's Applicant Information Notice
 
 
 To support efficiency, TRIO may use limited AI tools during the candidate review process. All hiring decisions are made by people, not AI.
 
 
 To ensure fairness and an accurate understanding of your skills, we ask that candidates refrain from using AI tools or AI‑generated responses during interviews or assessments. We want the opportunity to get to know you and your experience.
 
 
 Teamwork
 
 
 <ul>
 <li>
 Passion
 </li>
 <li>
 Integrity
 </li>
 <li>
 Innovation
 </li>
 </ul>
</div>

ICON plc

<div></div><div><div>What You Will Be Doing:</div><div></div><ul><li>
Serve as the primary point of contact between investigational sites and the sponsor</li><li>
Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out</li><li>
Ensure site compliance with ICH-GCP, SOPs, and regulations</li><li>
Maintain up-to-date documentation in CTMS and eTMF systems</li><li>
Support and track site staff training and maintain compliance records</li><li>
Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting</li><li>
Support subject recruitment and retention efforts at the site level</li><li>
Oversee drug accountability and ensure proper storage, return, or destruction</li><li>
Resolve data queries and drive timely, high-quality data entry</li><li>
Document site progress and escalate risks or issues to the clinical team</li><li>
Assist in tracking site budgets and ensuring timely site payments (as applicable)</li><li>
Collaborate with cross-functional partners including CTAs, LTMs, and CTMs</li></ul><div></div><div>
You are:</div><ul><li>
A graduate with a Bachelor&rsquo;s degree in Life Sciences or equivalent, or a qualified RN</li><li>
Eligible to work in United States without visa sponsorship</li><li>
A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry</li><li>
Experienced monitoring Oncology Hematology clinical trials</li><li>
Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF</li><li>
A clear communicator, problem-solver, and collaborative team player</li><li>
Willing and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Los Angeles, CA near major HUB airports to support efficient regional travel</li></ul></div><div></div>

UCLA Health

<div><div>Description
Life-saving breakthroughs, innovative therapies, and next-generation technologies. Through vision, tenacity, and inspiration, UCLA Health&rsquo;s world-class researchers are redefining human health and patient care. Join us and live out your passion for discovery while making an incredible difference in the lives of people around the world.

The incumbent will support a wide range of clinical research activities under the guidance of the Principal Investigator. Responsibilities include managing human subject regulatory requirements&mdash;such as ARC and IRB submissions, tracking adverse events, ensuring FDA compliance, and coordinating DSMB activities. The role also oversees participant recruitment, screening, enrollment, and retention. Additional duties include organizing and analyzing study data, generating summary figures and tables, contributing to presentations and manuscripts, and reviewing and entering chart data into study databases. Prior research experience is preferred, and experience coordinating multi site clinical studies is highly beneficial. All work will be performed under the supervision of the Principal Investigator or senior scientific staff.

Salary: $31.21 - $50.21 hourly</div><div>
Qualifications
Required:<ul><li>
Excellent skills in computer and software operation 
</li><li>
Knowledge and experience using word processing, spreadsheet (Microsoft Word/Excel) 
</li><li>
Proven track record of working with high level of accuracy. 
</li><li>
Demonstrated ability to write clear, concise, and grammatically correct letters, memos, and emails. 
</li><li>
Excellent ability to perform a variety of duties with frequent interruptions and to work effectively under conditions of fluctuating workload. 
</li></ul><div>
Preferred: 
</div><div><ul><li>
Bachelor&rsquo;s Degree and/or equivalent combination of education and experience. 
</li><li>
Previous experience in data management of clinical research protocols, including the completion of case report forms and other study documents. 
</li><li>
Knowledge of health services or clinical research methodology and principles. 
</li><li>
Prior IRB experience and coordination of clinical studies desired. 
</li><li>
Experience working with a diverse research population. 
</li><li>
Knowledge of simple statistical analysis. 
</li><li>
Excellent scientific writing skills in order to write or edit correspondence, progress reports, and research papers 
</li><li>
Knowledge and experience using statistical analysis software 
</li><li>
Knowledge of basic statistical tests and procedures related to data management and selection of descriptive tests for summarizing data. 
</li><li>
Knowledge of the rules and regulations for Human Subject Protection and informed consent</li></ul></div></div></div><div></div>

Staff Research Associate II - VA

Keck Medicine of USC

<div>The Senior Analyst of Clinical Operations Business Intelligence (COBI) leads knowledge management efforts to redesign care processes to optimize value (improve outcomes, patient satisfaction and reduce cost). This role provides strategic oversight for the development and governance of analytics dashboards that provide a single source of truth for reliable, meaningful and actionable insights. The Senior Analyst leads complex assessment and diagnostic of problems, architect scalable data analytics solutions, develops performance dashboards, and manages structured improvement initiatives, from transformational projects, to focused analytics development improvement events. The Senior Analyst also acts as a coach for his/her team and for any colleagues they interact with to help them establish mechanisms to sustain performance after the completion of projects. The Senior Analyst establishes and sustains strategic relationships with physicians, nurses, other clinicians and administrators to build support for change and sustainability efforts. This role leads cross-functional collaboration to translate clinical and operational requirements into scalable analytics solutions, understand process flow and design the analytics tools they need to make data-driven decisions to improve patient care, drive down cost, and increase revenue. The Senior Analyst leads the development of management mechanisms and systems to build the knowledge management capacity of the medical enterprise. The Senior Analysts strengthens data and analytics support across the USC health system to foster its continued growth, increased efficiency, development of workflows in conjunction with physicians and establishes strategic relationships with referring facilities. These efforts will improve the transitions of care resulting in safer, more efficient care with better patient and family experience, reduced length of stay and readmissions. The scope of activities for the Senior Analyst include: cultivating strategic customer relationships, serving as a trusted analytics advisor to operational leaders, leading agile design while developing business solutions with clinical stakeholders, building complex analytical models (e.g., predictive models using machine learning techniques, automating multi-source data capture and analysis, leading high-impact performance improvement and operations projects in the organization, providing actionable insights, and employing the advanced analytical judgment necessary to determine the accuracy and applicability of analytical conclusions.
Essential Duties:<ul><li>
Lead the design, development and optimization of management tools based on business and clinical requirements to improve value aligning with organizational goals and objectives Develop solutions that embed and extract relevant patient information into and from health information systems, in order to provide effective communication that will support quality, process improvement, and operations initiatives as they relate to clinical care, program development, and training</li><li>
Applies advanced engineering and data science principles and concepts in planning, coordinating and executing operational and research activities Provides data science expertise to support data-driven decision making Performs complex analysis to produce meaningful insights and actionable analysis to track clinical operations performance at all levels in the organization leveraging evidence-based benchmarking identified by key performance indicators. Socializes tools and initiatives across the health system. Lead cost modeling, financial impact analysis, capacity planning and other services related to daily operations and clinical program growth Oversee development, automation and governance of reporting frameworks and executive presentations, ensuring data quality, standardization, and scalability</li><li>
Develops collaborative relationships with physicians, administrative leaders and frontline staff to aid in their understanding of data and plan improvements to clinical operations.</li>
Performs duties including some or all of the following: Lead projects/tasks by creating detailed work plans with identified timelines/milestones and objectives/targets, aligning with allocated resources and organizational strategy Implements planned projects in consultation with appropriate leadership and identified stakeholders, ensuring all work is properly maintained and kept confidential when applicable Controls project by maintaining alignment with organizational policies/procedures and regulatory compliance standards Analyze and manage risks and issues associated with technical operations on all programs and medical technology project implementations. Lead, mentor, and review team deliverables to ensure high-quality outputs, adherence to best practices, and alignment with clinical, operational, and organizational priorities. Recommend and/or implement methods and techniques to address a variety of engineering, management, and regulatory requirements on the use of medical data. Evaluates project by ensuring deliverables are on time, within budget, and at the required level of quality by tracking established process and outcome measure to targets Conducts assessments and collects data to support department initiatives. Audits compliance to new policy, protocols and practices. Develops return on investment (ROI) formulas and calculations to measure project impact.<li> Attends promptly to the administrative details of the position including preparation of Performance Reports</li><li>
Performs data collection and/or entry processes. Recommends, utilizes and enhances methods and procedures for data acquisition, management and quality control, as needed. Apply advanced statistical modeling, predictive analytics, and data science techniques for data analysis, as needed. Resolves complex problems, answers questions and provides information to facilitate process. Uses standard statistical analysis software, as needed</li><li>
Performs other related duties as assigned or requested.</li></ul>
Required Qualifications:<ul><li>
Req Bachelor&rsquo;s Degree Degree in engineering, computer engineering, or data science</li></ul><ul><li>
Req 3-5 years experience in business/ data analytics, healthcare analytics, healthcare quality, clinical and operations decision support or related field.</li><li>
Req 1 - 2 years in a lead/senior role.</li></ul><ul><li>
Req Working knowledge of back-end databases (e.g., relational designs) spreadsheets, word processing, statistical software, analytical models, data science principles and application, and data visualization programs (e.g., Tableau, Qlikview, Qliksense, Power BI).</li><li>
Req Knowledge of business (operational, clinical and financial) statistics and data analyses techniques.</li><li>
Req Expert knowledge in Python, R, and/or SQL software programming</li><li>
Req Ability to manage, analyze, and derive clinical and operational insights from health system information technologies.</li><li>
Req Strong analytical thinking and problem solving skills.</li><li>
Req Demonstrated leadership capabilities, including but not limited to: o Developing dynamic, constructive working relationships and partnerships with operational and clinical partners. o Excellent interpersonal skills (negotiation, listening and communication skills) characterized by effective interactions with a diverse range of internal and external constituents, stakeholders and audiences. o Relationship driven, consultative, a team player, able to effectively lead process improvement initiatives. o Possesses a good understanding of Business Intelligence tools, technology platform, and related systems to handle queries about clinical and business data/analytical solutions. o Be adept at presenting technical materials to a non-technical audiences, applying human factors principles and user centered design principles, understanding user workflows, applying statistical methods latforms such as Qlikview and Tableau</li></ul>
Preferred Qualifications:<ul><li>
Pref Master&rsquo;s degree Degree (Health Administration, Nursing, Industrial Engineering, Analytics)</li><li>
Pref Expertise in data science, including machine learning approaches to produce predictive models;</li><li>
Pref Proficiency in statistical approaches;</li><li>
Pref Master level expertise in data visualization platforms such as Qlikview and Tableau</li></ul>
Required Licenses/Certifications:
<ul><li>Req Fire Life Safety Training (LA City) If no card upon hire, one must be obtained within 30 days of hire and maintained by renewal before expiration date. (Required within LA City only)</li></ul> 

The annual base salary range for this position is $81,120.00 - $133,010.00. When extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate&rsquo;s work experience, education/training, key skills, internal peer equity, federal, state, and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations.
<div>Job ID REQ20173362 Posted Date 03/18/2026</div></div>

Clinical Operations Business Intelligence Analyst, Senior - Value Improvement Office - Full Time 8 Hour Days (Exempt) (Non-Union)

Explore 351+ Senior clinical research associate in Los Angeles this March. Find roles across top companies and apply now to boost your career.

351 senior clinical research associate jobs In Los Angeles

Senior CRA

Heart Institute Clinical Research Associate I - Cheng Lab

Clinical Research Associate

Clinical Research Associate

Clinical Research Associate

Staff Research Associate II - VA

Clinical Operations Business Intelligence Analyst, Senior - Value Improvement Office - Full Time 8 Hour Days (Exempt) (Non-Union)