Clinical Trials Analyst
3 days ago
Description
The Clinical Trials Analyst is responsible for regulatory coordination of clinical research studies within assigned units, departments or divisions. You will perform detailed review of clinical research protocols and utilize that information to prepare, manage and submit all required study/regulatory documents and all required applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, etc. You will work with study monitors to process, review, and collect the appropriate regulatory documents in a timely manner and in compliance with federal, state, and university mandated regulations and policies.
Salary Range: $30.56 - $60.82/Hourly
Please note, this is a part-time, one year limited position that may convert to career.
Qualifications
Required:
- Minimum of 1+ years of experience as a clinical researcher.
- Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.
- Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.
- Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.
- Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.
- Organization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met.
- Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.
- A learning and professional growth mentality so new software tools, systems, and processes can be adopted quickly and efficiently.
- Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.
- Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.
Preferred:
- Bachelor’s degree.
-
Senior Clinical Trial Manager
1 month ago
Boston, MA, United States Clinical Dynamix Full timeSenior Clinical Trial ManagerDescriptionReporting to the Director, Clinical Operations, the Senior Clinical Trial Manager is responsible for leading the execution of clinical studies on schedule and on budget. The Senior Clinical Trial Manager ensures studies are conducted efficiently and with quality, adhering to timelines and budget, and in alignment with...
-
Clinical Trial Manager, Start Up
1 month ago
Boston, MA, United States Clinical Dynamix Full timeClinical Trial Manager, Start Up Job Description; (Hybrid in office 3 days peer week)At Company, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team’s expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic...
-
Clinical Trial Rater
3 days ago
Los Angeles, CA, United States M3 Wake Research, Inc. Full timeCompany Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is...
-
Clinical Trials Manager
2 weeks ago
Los Angeles, United States Immix Biopharma (Nasdaq: IMMX) Full timeWho We Are Immix Biopharma, Inc. (ImmixBio) (Nasdaq: IMMX) is a clinical-stage biopharmaceutical company trailblazing cell therapies in oncology and autoimmune diseases. Our lead cell therapy asset is next generation CAR-T NXC-201 for relapsed/refractory AL Amyloidosis, and relapsed/refractory multiple myeloma, currently being evaluated in our ongoing...
-
Clinical Trials Manager
2 weeks ago
Los Angeles, United States Immix Biopharma (Nasdaq: IMMX) Full timeWho We Are Immix Biopharma, Inc. (ImmixBio) (Nasdaq: IMMX) is a clinical-stage biopharmaceutical company trailblazing cell therapies in oncology and autoimmune diseases. Our lead cell therapy asset is next generation CAR-T NXC-201 for relapsed/refractory AL Amyloidosis, and relapsed/refractory multiple myeloma, currently being evaluated in our ongoing...
-
Clinical Trials Program Manager
1 week ago
Los Angeles, California, United States Immix Biopharma (Nasdaq: IMMX) Full timeAbout UsImmix Biopharma (Nasdaq: IMMX), a clinical-stage biopharmaceutical company, is revolutionizing cell therapies in oncology and autoimmune diseases. Our lead asset, NXC-201, aims to be the world's first single-day CAR-T, enhancing patient care and paving the way for expansion into autoimmune indications.We're a team of dedicated professionals working...
-
Clinical Trial Manager II Position
2 weeks ago
Los Angeles, California, United States Lifelancer Full timeJob Title: Clinical Trial Manager IIJob Location: United StatesJob Type: Remote Full-time JobJob Level: Mid-Senior levelSalary: $120,000 - $150,000 per yearClinical Trials are a crucial part of the drug development process. As a Clinical Trial Manager II at ICON, you will be responsible for delivering trials on time, within budget, and with the highest...
-
Director, Business Development
3 days ago
, WI, United States Worldwide Clinical Trials Full timeRequisition Number: 7812 Employment Type: Regular Who we are Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific...
-
Clinical Trial Manager
4 days ago
San Diego, CA, United States CEDENT Full timeSummary: The Clinical Trial Manager (CTM) is responsible for managing and supporting clinical trials in compliance with applicable regulations, ICH/GCP guidelines, and standard operating procedures (SOPs). The CTM works collaboratively with cross-functional teams and partners with internal and external stakeholders to align activities with study goals and...
-
Senior Research Scientist
1 week ago
Los Angeles, California, United States CEDARS-SINAI Full timeJob OverviewCedars-Sinai, a renowned leader in healthcare, seeks a highly skilled Senior Research Scientist to join its team. As a key member of our clinical trials unit, you will play a pivotal role in advancing medical research and improving patient care.This is a full-time position with a competitive salary range of $66,600-$108,000 per annum, based on...
-
Senior Trial Attorney
1 month ago
Los Angeles, CA, United States Huntress Talent Full timeLitigation AttorneyHybridLocation - Century City, LASeeking a Litigation Attorney to join a boutique law firm in Century City. The ideal candidate will be responsible for managing all aspects of a case in both state and federal court, including pre-trial preparation, court appearances, motions, depositions, mediations, negotiations, and trial. Could be tax,...
-
Los Angeles, California, United States Lifelancer Full timeOverview">Kelly Science Clinical is seeking a Clinical Trial Supply Coordinator for a fulltime contract-to-perm position with a biopharmaceutical client. The ideal candidate will have strong knowledge of regulatory requirements and industry standards related to clinical trial supplies.">Job Summary">The Clinical Trial Supply Coordinator will be responsible...
-
Data Management Specialist for Clinical Trials
2 weeks ago
Los Angeles, California, United States University of Southern California Full timeThe University of Southern California (USC) is a renowned research university that values diversity and is committed to equal opportunity in employment. As a clinical trials data specialist, you will be part of a world-class team that conducts cutting-edge research.Job SummaryThis position involves working with medical records, extracting relevant data, and...
-
Clinical Trials Manager
2 weeks ago
San Mateo, CA, United States Fusion Life Sciences Technologies LLC Full timeClinical Trials Manager Is this your next job Read the full description below to find out, and do not hesitate to make an application. Job Location: Foster City, CA Job Duration: 6 months visa Green Cards and USA citizens manager is looking for local candidates POSITION OVERVIEW: Clinical Operations is responsible for the worldwide execution of all Phase...
-
Clinical Trial Associate
3 days ago
Boston, MA, United States CEDENT Full timeJob description PURPOSE OF THE FUNCTION As a member of the Clinical Trial Team (CTT), the Clinical Trial Associate Level 1 (CTA) will assist the Clinical Trial Managers (CTM) and other CTT functions if deemed necessary with the conduct of the assigned clinical trials, including the administration, coordination, and archival. This person will also assist...
-
Los Angeles, California, United States Lifelancer Full timeAbout LifelancerLifelancer is a pioneering talent-hiring platform in the Life Sciences, Pharma, and IT sectors. We connect talented professionals with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.Job Title: Clinical Trial Supply Coordinator-West CoastOverview:The Clinical Trial Supply Coordinator will play a...
-
Cardiovascular Research Specialist
5 days ago
Los Angeles, California, United States CEDARS-SINAI Full timeAbout the RoleWe are seeking a highly skilled Cardiovascular Research Specialist to join our team at Cedars-Sinai. As a key member of our clinical trials unit, you will be responsible for managing all lab activities, including financial management, human resource management, and general administration.Key ResponsibilitiesProject Planning and ExecutionYou...
-
Los Angeles, CA, United States Kaiser Permanente Full timeJob Summary: Manages day-to-day activities of a major segment(s) of medium to large studies or several smaller studies. May supervise project staff. Works under general supervision. Final review required for some phases of projects.Essential Responsibilities: Manages day-to-day activities of a major segment(s) of medium to large studies or several smaller...
-
Director of Business Development
3 days ago
California, MO, United States IMA Clinical Research, Inc. Full timeCompany Overview: The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies. Our team of seasoned professionals collaborates with industry leaders, conducting patient-centric research across diverse therapeutic areas. Committed to ethical practices and...
-
Clinical Trial Manager
1 month ago
Baltimore, MD, United States Catalyst Life Sciences Full timeCatalyst Life Sciences is currently partnered with a global medical research organization for their oncology clinical research division based in the Baltimore, MD area.Day to day you will:Design and manage a project by monitoring timelines, budgets and other considerationsCoordinate with lead scientists, business developers, other clinical trial managers and...