Clinical Trial Specialist

4 weeks ago


Los Angeles, California, United States Barrington James Full time

Part-Time Clinical Trial Specialist Opportunity


Barrington James is seeking a skilled Clinical Trial Specialist to support our client with clinical site agreement negotiations and general support with agreements.


Key Responsibilities:


  • Ensure effective negotiation and ongoing management of clinical trial agreements with investigative sites.
  • Collaborate with Clinical Operations and Project Management to facilitate timely site start-up for clinical trials, including accurate forecasting of contract execution timelines.
  • Work closely with the Functional Manager and other compliance departments to ensure adherence to laws and regulations, minimizing risks in clinical trials.
  • Effectively communicate and clarify legal and budgetary issues to both internal and external stakeholders, in accordance with departmental guidelines.
  • Review and assess client-initiated contract changes and escalate deviations as necessary, following department protocols.
  • Partner with the team to prioritize tasks and adjust priorities based on evolving business needs and client requirements.
  • Evaluate contracts to ensure completeness and accuracy while conforming to department guidelines; make necessary corrections and document changes.
  • Participate in client meetings to expedite the contract signing process as directed.
  • Record all site interactions in the database promptly and accurately, ensuring comprehensive status updates.


Requirements:


  • 1-3 years of experience with contracts.
  • Bachelor's Degree or Juris Doctor (JD) required.
  • Proficiency in reading, writing, and speaking fluent English.
  • Understanding of clinical contracts.
  • Experience in relevant areas such as contracts, negotiation, or sales.
  • Familiarity with working in a service industry or project management environment.


This role requires legal authorization to work in the US. We are not currently accepting work visas.

Apply now by submitting your CV.



  • Los Angeles, California, United States Keck School of Medicine Full time

    Clinical Trial Management System SpecialistThe Keck School of Medicine is seeking a highly skilled Clinical Trial Management System Specialist to join our team. As a key member of our Clinical Trials Office, you will be responsible for building and configuring electronic study calendars with budget details for clinical trial data capture in accordance with...


  • Los Angeles, California, United States SciPro Inc. Full time

    Clinical Trial Coordinator SciPro Inc. is seeking a highly motivated and detail-oriented Clinical Trial Coordinator to support the execution of clinical trials. The ideal candidate will have a Bachelor's degree in biological sciences or a related field, at least 3 years of experience in the pharmaceutical or biotech industry, and proficiency in Microsoft...


  • Los Angeles, California, United States Bayside Solutions Full time

    Clinical Trial Manager OpportunityW2 Contract-to-HireSalary Range $156,000 - $176,800 per yearRedwood City, CA - Hybrid or Remote PSTJob OverviewThis is a unique opportunity for an experienced Clinical Operations Professional to manage Phase I-III clinical trials within an industry setting. The ideal candidate will have a solid understanding of clinical...


  • Los Angeles, California, United States Agilent Technologies Full time

    Clinical Trial Manager Job DescriptionThe Clinical Trial Manager will play a key role in the successful execution of clinical trials, working closely with the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team. This includes managing the day-to-day execution of clinical studies for in vitro diagnostics (IVDs) and medical devices (MDs),...


  • Los Angeles, California, United States Kaiser Permanente Full time

    Research Associate II, Clinical Trials Specialist**Job Summary:**We are seeking a highly skilled Research Associate II, Clinical Trials Specialist to join our team at Kaiser Permanente. This role will be responsible for coordinating day-to-day activities of several small-scale projects or phases of one or more larger projects. The ideal candidate will have a...


  • Los Angeles, California, United States University of California Full time

    Job Title: Clinical Trials CoordinatorThe Department of Urology at the University of California is seeking a highly skilled and organized Clinical Trials Coordinator to join our team. In this role, you will assist the Clinical Research Coordinator and/or Senior Clinical Research Coordinator in managing clinical research/trial/study activities, prioritizing...


  • Los Angeles, California, United States UCLA Health Full time

    Job Summary:The Division of Pediatric Infectious Diseases at UCLA Health is seeking a Quality Assurance Manager to implement clinical trials protocols and coordinate laboratory-related committees and working groups.Key Responsibilities:Review protocol testing, laboratory quality assurance information, and support capabilities required to conduct global...


  • Los Angeles, California, United States University of California Full time

    Job Title: Quality Assurance ManagerThe Division of Pediatric Infectious Diseases at the David Geffen School of Medicine at UCLA Health is seeking a Quality Assurance Manager to implement clinical trials protocols and coordinate laboratory-related committees and working groups.Key Responsibilities:Review and implement clinical trials protocolsCoordinate...


  • Los Angeles, California, United States Clemente Clinical Research Full time

    Job OverviewClemente Clinical Research is seeking an experienced Clinical Research Coordinator to join our team. As a key member of our research team, you will work closely with renowned doctors and researchers to coordinate and manage clinical trials.Key Responsibilities:Coordinate and manage clinical trials, including patient recruitment, screening, and...


  • Los Angeles, California, United States Children's Hospital Los Angeles Full time

    Purpose and SummaryThe Coordinator, Clinical Trial Operations (CTO) plays a pivotal role in managing multi-center clinical and research studies. This individual must possess a broad spectrum of knowledge and experience in conducting clinical trials, with the ability to work independently and coordinate consortium activities at the central operations...

  • Medical Assistant

    2 weeks ago


    Los Angeles, California, United States Orange County Neuropsychiatric Rese Full time

    Job Title: Medical Assistant - Clinical TrialsWe are a leading research site specializing in CNS (Central Nervous System) clinical trials, seeking a highly skilled Medical Assistant to join our team.Key Responsibilities:Perform routine clinical tasks to support medical staff, including ECG and vital signs collection.Assist Clinical Research Coordinators with...


  • Los Angeles, California, United States BioSpace, Inc. Full time

    Job Title: Senior Clinical Trial Manager ConsultantWe are seeking an experienced and dynamic Senior Clinical Trial Manager Consultant to join our team at ReCode Therapeutics. As a key member of our clinical operations team, you will be responsible for implementing global clinical operations strategy for our programs, collaborating with Clinical Operations...


  • Los Angeles, California, United States Orange County Neuropsychiatric Rese Full time

    We are seeking a highly organized and detail-oriented Medical Research Assistant to join our team at Orange County Neuropsychiatric Research. As a key member of our clinical trials team, you will be responsible for performing routine administrative and clinical tasks to ensure the smooth operation of our research clinic.Key Responsibilities:Perform routine...


  • Los Angeles, California, United States Orange County Neuropsychiatric Rese Full time

    We are seeking a highly organized and detail-oriented Medical Research Assistant to join our team at Orange County Neuropsychiatric Research. As a Medical Research Assistant, you will play a critical role in supporting our clinical trials by performing routine administrative and clinical tasks.Key Responsibilities: Perform routine clinical tasks to support...


  • Los Angeles, California, United States DirectEmployers Full time

    Amergis Healthcare Staffing seeks a Clinical Research Nurse to lead clinical trials. This role functions as a clinical investigator, sub-investigator, clinical researcher, research nurse, administrator, coordinator, consultant, or educator in clinical trial management. The Clinical Research Nurse is involved in one or more aspects of clinical trials...


  • Los Angeles, California, United States Clemente Clinical Research Full time

    Job OverviewClemente Clinical Research is seeking an experienced Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in the success of our clinical trials by ensuring the smooth execution of study protocols, managing data, and maintaining accurate records.Key Responsibilities:Coordinate and manage...


  • Los Angeles, California, United States Matrix Clinical Research Full time

    Job Title: Clinical Research Medical AssistantJob Summary:Matrix Clinical Research is a leading organization in the field of clinical research, dedicated to advancing medical knowledge and improving patient outcomes. We are seeking a detail-oriented Clinical Research Medical Assistant to join our dynamic team.Key Responsibilities:Recruit, screen, and enroll...


  • Los Angeles, California, United States University of California Full time

    Job SummaryThe University of California seeks a highly organized and detail-oriented Clinical Trials Research Administrator to support the Department's research initiatives. The successful candidate will be responsible for pre-award administration, ensuring timely and accurate processing of research awards.Key ResponsibilitiesManage pre-award administration...


  • Los Angeles, California, United States Aequor Technologies Full time

    Job Title: LPN-ODR -Felony Incompetent to Stand Trial Program SpecialistJob Summary: Aequor Technologies is seeking a Licensed Vocational Nurse (LVN) to work on the Felony Incompetent to Stand Trial (FIST) Diversion and Community Based Restoration program. The ideal candidate will have a minimum of one (1) year of recent clinical experience and be...


  • Los Angeles, California, United States Amerit Consulting Full time

    Job Title: Clinical Research Coordinator - Regulatory SpecialistJob Summary:Amerit Consulting is seeking an experienced Clinical Research Coordinator - Regulatory Specialist to join our team. The ideal candidate will have a strong background in regulatory affairs and clinical trials, with a proven track record of success in coordinating studies and ensuring...