Clinical Trial Assistant
$26 - $31 per hourKimball,-Tirey-
We are an established real estate law firm with offices across California. Our Los Angeles office is looking for a Trial Department Assistant to join our fast-paced team. If chosen as the successful candidate, you will be responsible for ensuring the efficient and timely production of all pre-trial and post-trial documents in the trial phase of the unlawful detainer process.About UsWith almost 50 years in the California legal industry and six offices statewide, our firm was founded on a commitment to customer service that has flourished within our culture of inclusion and diversity. We believe in working hard for our clients each day and in taking care of our employees so they are empowered to do their very best work. It is our mission to provide the highest quality, cost-effective legal services to our clients.Compensation Range:$26.00-$31.00/hour (DOE)Responsibilities:Process trial results and update ProLawDraft, Serve and E-File Court ordered noticesAdd trial dates to ProLaw and calendarCommunicate with and respond to clients and courts via email and phoneE-Filing documentsFollow up with clients regarding stipulation complianceMaintain communication with attorneys regarding upcoming court casesContact clients prior to trial to confirm dates, times, and court locationsMake calls to court to follow up on mattersPreparing cases for trial including but not limited to preparing case summaries, reviewing discovery and gathering evidenceManage attorney’s calendars for court and trial datesMaintain and address all incoming emails in a timely mannerPerform other duties as assignedQualifications:We are looking for candidates with the following qualifications:2+ years of legal or law firm experienceAbility to manage a high-volume workloadAbility to multi-task and complete work in a timely and efficient mannerExperience with e-filingStrong communication skills and attention to detailMinimum typing speed of 50 words per minuteFamiliarity with Microsoft Word and PDF editorThe following qualifications are preferred:Formal legal training and/or trial experienceEssential Forms and ProLaw efficiencyKnowledge of unlawful detainers and local county court rules and proceduresSchedule:Position is full-time at 40 hours/week. Our business hours are 8:30am-5:30pm Monday-Thursday, 8:30am-5:00pm Friday.We currently offer a hybrid work model for select position within the Firm. New Hire employees who are offered a hybrid schedule will complete their onboarding and training in-office as deemed necessary for the position by the firm before transitioning to a hybrid schedule, subject to approval by their supervisor.Why Work for Us?Our firm offers a rewarding work environment that values a work-life balance and fosters a culture of professional growth and opportunities. We provide a comprehensive compensation package that includes medical, dental, vision, life, disability insurance, 401(k), paid vacation, and sick time.What employees are saying about working with us:“The people, atmosphere, culture, and work/life balance are great.”“I always feel included, respected, and a part of the team.”“I have been given so many opportunities to grow and have learned so much.”Application Process:Candidates who meet the criteria for the position will be contacted for the next step in the hiring process. Interviews are currently being conducted by phone or video with possible in-person interviews for finalist candidates.We are an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status. #J-18808-Ljbffr
- The University of California - Los Angeles Health is seeking an Assistant Clinical Research Coordinator to assist in the operational management of clinical trials and studies. Key responsibilities include managing project tasks, ensuring protocol adherence, and supporting...Suggested
$91.34k - $114.17k
Clinical Research Associate - Oncology - West RegionICON is a global healthcare intelligence and clinical research organisation united... ...pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities...SuggestedFull timeLocal area$99.1k - $141.89k
The Clinical Investigations Support Office provides support to the investigators in conducting cancer-related clinical trials at the USC Norris Comprehensive Cancer Center and its affiliated locations... ....• Contact potential patients to assist with scheduling oncology...SuggestedFull timeWork experience placementWork at officeLocal areaFlexible hours- Senior Clinical Research Associate - Cardio (Smart Pulse A-fib) - All RegionsICON is a global... ...teams and sites.Well-versed in clinical trial management. They are rigorous, detail-... ...and disability coverageEmployee assistance programmes and wellbeing resourcesLearning...SuggestedFull time
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Southern CaliforniaICON is a global healthcare... ...activities throughout the clinical trial lifecycle. This Sr. CRA role will support... ...and disability coverageEmployee assistance programmes and wellbeing resourcesLearning...SuggestedFull timeInterim roleLocal areaRemote work$33.65 - $48.08 per hour
...Represents the Bank at various community events and fundraisers, acts as a champion for the CRA team at internal meetings and/or events. Assist with participating in CRA service activities and other assignments that contribute to the implementation and maintenance of an...Full timeWork at officeFlexible hours- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading... ...Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator... ...accommodations, when appropriate, to assist employees or applicants to perform the essential...Contract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...out visits) in accordance with contracted scope of work and Good Clinical Practice.Work with sites to adapt, drive, and track subject... ...originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File...Local area
- ....What will you be doing in this role?The Clinical Research Associate I works directly with... ...forms, entering clinical research data, and assist with regulatory submissions to the IRB.... ...federal guidelines.Assists with clinical trial budgets.Assists with patient research billing...Local areaShift workDay shift
- ...Clinical Research Associate IIThis role is designed to be 100% onsite, giving you the opportunity... ...of current research participants, assisting in IRB submission activities, budget and... ...participants for various clinical trials. Schedules research participants for research...Local areaRemote work
$25 - $35 per hour
...Clinical Research CoordinatorThe Research Coordinator will assist an Investigator, Research Associate, or Project Manager with operationalizing the tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection...Temporary work- ...Job Title Responsible for providing Clinical Research support for all clinical trials. Job Information Date Opened 04/02/2026 Job Type: Full time... ...Duties And Responsibilities Participate and assist in design and preparation of protocols and case report...Full timeWork experience placement
$91.34k - $114.17k
...Clinical Research Associate - Early Stage Development - West Region ICON plc is a world... ..., you will design and analyze clinical trials, interpreting complex medical data, and... ...for the years ahead. Global Employee Assistance Programme, LifeWorks, offering 24-hour access...Work experience placementRemote workFlexible hours$70 - $75 per hour
...Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region (ideally based out of Boston... ...sick time, and paid company holidays. We also offer an Employee Assistance Program (EAP) that provides services like virtual counseling,...Hourly payContract workPart timeLocal areaRemote work$91.34k - $114.17k
Clinical Research Associate - Oncology - West Region ICON plc is a world-leading healthcare intelligence and clinical research organization... ...progress and elevate risks or issues to the clinical team Assist in tracking site budgets and ensuring timely site payments (as...Work experience placementLocal areaVisa sponsorshipFlexible hours- ...leading healthcare institution in Beverly Hills is looking for a Clinical Research Coordinator to manage research projects and maintain... ...protocols, developing budgets, and ensuring funding throughout trials. This role offers a chance to work with a diverse team committed...
- Cedars-Sinai Medical Center is seeking a Clinical Research Associate I to work with the study team to coordinate and implement research... ...from source documents, enter data into electronic systems, and assist with regulatory submissions to the IRB and budget processes. A...
$22 - $30 per hour
Clinical Research Assistant in Los Angeles, CA (90067) Summary The Research Assistant I supports the planning, coordination, and execution of clinical research studies under the direct supervision of the Site Director or Clinical Research Coordinator (CRC). This role assists...Work at officeMonday to FridayFlexible hours- Responsibilities Collects, evaluates and/or abstracts clinical research data. May assist in designing forms for data collection/abstraction. Enters and... ...with local and federal guidelines. Assists with clinical trial budgets and patient research billing. Responsible for...Local area
$20 - $32 per hour
...and endless growth opportunities. We are actively hiring Clinical Research Assistants at the Century City/Panorama City site locations. This is... ...Angeles area. These locations are formerly Valkyrie Clinical Trials—we are proud to welcome Valkyrie Clinical Trials to the...Work at officeMonday to FridayShift work$140k - $165k
...Primary Objective of Position The Senior Clinical Research Associate (Sr. CRA) is... ...investigative sites for all assigned clinical trial-related activities, to ensure trials are... ...investigators and other site staff Assists site staff in maintaining audit/inspection...Full timeInterim roleWork at officeRemote workWork from homeHome officeMonday to FridayNight shiftWeekend workAfternoon shift- Cedars-Sinai is seeking a Clinical Research Associate I to work with research teams at the Smidt Heart Institute. This position involves coordinating clinical studies, evaluating data, and ensuring compliance with research protocols. Applicants should have at least a high...
- Cedars-Sinai's Smidt Heart Institute in Los Angeles invites applications for a Clinical Research Associate I/CPT. You will assist in coordinating noncomplex research studies under supervision, supporting data collection, regulatory submissions, budgeting, and study logistics...
- ICON Strategic Solutions in Los Angeles is seeking a Clinical Research Associate to conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. You will ensure protocol compliance, data integrity, and patient safety throughout the trial...
- ...improving patient outcomes. Job Summary The Clinical Research Associate I works directly with... ..., entering clinical research data, and assist with regulatory submissions to the IRB. Provides... ...guidelines. Assists with clinical trial budgets and patient research billing as needed...Work at officeLocal area
$96.2k - $151.4k
...primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated... ...ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring...For contractorsLocal areaRemote work2 days per week3 days per week$83.3k - $138.8k
...The Senior Internal Clinical Research Associate is a s upporting role for the Clinical Research team, mainly focused on trial conduct and site management activities in the U.S. following good clinical practice and all applicable regulations. This position will work...Full timeContract work$80k - $130k
What This Is You own IVD diagnostic clinical studies end-to-end — site activation through data lock — across multiple active trials at once. You are not a monitor who writes reports. You are the person who makes studies move. The Culture RDI runs sample collection studies...$65 - $90 per hour
Overview C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the Los Angeles region. This opportunity is well-suited for professionals who enjoy working closely with investigative sites while ensuring high-quality...Hourly payRemote work- ...Clinical Research Data Associate IIAt Cedars-Sinai, we pride ourselves on our inclusive and collaborative culture. We are committed to... ...analysis, and work with bioinformatics to develop and maintain trial management systems. Ensures compliance with all federal and local...Local areaRemote work1 day per week
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