We have other current jobs related to this field that you can find below

  • Sr. Clinical Research Specialist

    4 weeks ago

    Irvine, United States Johnson & Johnson Full time

    Description Mentor Corporation, a member of the Johnson & Johnson Family of Companies, is currently recruiting a Sr. Clinical Research Specialist located in Irvine, CA.*There is already an identified candidate for the role.At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex...

  • Sr. Clinical Research Specialist

    4 weeks ago

    Irvine, California, United States Johnson & Johnson Full time

    Mentor Corporation, a member of the Johnson & Johnson Family of Companies, is currently recruiting a Sr. Clinical Research Specialist located in Irvine, CA.*There is already an identified candidate for the role.At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are...

  • Clinical Research Regulatory Specialist

    6 days ago

    Irvine, California, United States University Of California Irvine Full time

    Overview:Established in 1965, University of California, Irvine is recognized as a leading institution in the Association of American Universities and consistently ranks among the top public universities in the nation. With a vibrant community of over 36,000 students and a diverse array of 224 degree programs, UC Irvine is dedicated to academic excellence and...

  • Clinical Research Regulatory Specialist

    5 days ago

    Irvine, California, United States University Of California Irvine Full time

    Overview:Established in 1965, University of California, Irvine is a distinguished member of the Association of American Universities, consistently ranked among the top public universities in the nation. The institution is recognized for its academic excellence, innovative research, and vibrant campus life. With over 36,000 students and a wide array of degree...

  • Sr. Clinical Research Scientist

    3 weeks ago

    Irvine, United States Kelly Science, Engineering, Technology & Telecom Full time

    Senior Clinical Research Scientist This position is located in Irvine, CA (Hybrid Role)Qualifications:A minimum of a Bachelor’s degree with at least 5 years of clinical research experience requiredAdvance degree (Master’s degree, PhD, PharmD etc.) with 2-3 year of clinical or related research experience highly preferredA Life Science, Physical Science,...

  • Sr Clinical Research Scientist

    3 weeks ago

    Irvine, United States Kelly Science, Engineering, Technology & Telecom Full time

    Senior Clinical Research Scientist Qualifications:A minimum of a Bachelor’s degree with at least 5 years of clinical research experience requiredAdvance degree (Master’s degree, PhD, PharmD etc.) with 2-3 year of clinical or related research experience highly preferredA Life Science, Physical Science, Nursing, or Biological Science degree is...

  • Sr Clinical Research Scientist

    3 weeks ago

    Irvine, United States Kelly Science, Engineering, Technology & Telecom Full time

    Senior Clinical Research Scientist Qualifications:A minimum of a Bachelor’s degree with at least 5 years of clinical research experience requiredAdvance degree (Master’s degree, PhD, PharmD etc.) with 2-3 year of clinical or related research experience highly preferredA Life Science, Physical Science, Nursing, or Biological Science degree is...

  • Sr Clinical Research Scientist

    7 days ago

    Irvine, United States Kelly Services Full time

    Senior Clinical Research Scientist Qualifications: A minimum of a Bachelor’s degree with at least 5 years of clinical research experience required Advance degree (Master’s degree, PhD, PharmD etc.) with 2-3 year of clinical or related research experience highly preferred A Life Science, Physical Science, Nursing, or Biological Science degree is...

  • Clinical Research Associate Specialist

    2 weeks ago

    Irvine, United States Ledgent Technology Full time

    Assoc Clinical Research Specialist Duration - 6 Months, Contract, W-2 Location - Irvine, CA Pay - $30 - $45.05 an hour Summary:· Perform general study management support activities and assist in the processing of study/site/vendor payments in collaboration with Clinical Execution project teams.· Assist in the review, maintenance of study & site documents,...

  • Clinical Research Associate Specialist

    2 weeks ago

    Irvine, United States Ledgent Technology Full time

    Assoc Clinical Research Specialist Duration - 6 Months, Contract, W-2 Location - Irvine, CA Pay - $30 - $45.05 an hour Summary:· Perform general study management support activities and assist in the processing of study/site/vendor payments in collaboration with Clinical Execution project teams.· Assist in the review, maintenance of study & site documents,...

  • Clinical Research Coordinator

    1 week ago

    Irvine, United States Ledgent Technology Full time

    Medical Device client is seeking a Clinical Research Coordinator/Study Manager in Irvine, CA!Assoc Spec, Clinical ResearchDuration - 1 YearLocation - Irvine, CAMax Pay - $45.05 Summary: The main function of the Associate Clinical Research Specialist, is to perform study start-up and conduct activities, ensuring clinical studies are conducted and reported in...

  • Clinical Research Coordinator

    1 week ago

    Irvine, United States Ledgent Technology Full time

    Medical Device client is seeking a Clinical Research Coordinator/Study Manager in Irvine, CA!Assoc Spec, Clinical ResearchDuration - 1 YearLocation - Irvine, CAMax Pay - $45.05 Summary: The main function of the Associate Clinical Research Specialist, is to perform study start-up and conduct activities, ensuring clinical studies are conducted and reported in...

  • Administrative Assistant

    4 days ago

    Irvine, United States Irvine Clinical Research Full time

    Irvine Clinical Research is now hiring an Administrative Assistant. This is a patient-facing role at the front desk that supports our team of doctors and research professionals in our mission to find new medical breakthroughs through clinical research. Job Duties Warmly greet and assist study participants in reception areas at all times, especially older...

  • Associate Clinical Research Specialist

    1 week ago

    Irvine, United States Cynet Systems Inc. Full time

    Education and Experience Requirements: Bachelor's Degree or equivalent in a related field. 1 year of clinical research experience required. Additional Skills: Good computer skills in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery. Experience with electronic data capture...

  • Clinical Research Caregiver

    6 days ago

    Irvine, California, United States University Of California Irvine Full time

    About Us Established in 1965, University of California Irvine is a distinguished member of the Association of American Universities, consistently ranked among the top public universities in the nation. Our campus has produced five Nobel laureates and is recognized for its commitment to academic excellence, groundbreaking research, and innovation. With over...

  • Clinical Research Associate

    5 days ago

    Irvine, California, United States Cynet Systems Full time

    Job OverviewWe are seeking a Clinical Research Associate to support our client in their clinical research initiatives.Position Title: Clinical Research AssociateLocation: RemoteEmployment Type: ContractCompensation: $38.56/hr - $43.56/hrKey Responsibilities:Assist in the evaluation and upkeep of study and site documentation, aiding in the management of...

  • Lead Clinical Research Scientist

    5 days ago

    Irvine, California, United States Kelly Science, Engineering, Technology & Telecom Full time

    Senior Research Scientist in Clinical DevelopmentPosition Overview:This role involves a hybrid work model, providing flexibility while contributing to significant clinical projects.Qualifications:A Bachelor's degree in a relevant field is essential, accompanied by a minimum of 5 years of experience in clinical research.Preferred candidates will possess an...

  • HR Sr. Talent Development Specialist

    3 weeks ago

    Irvine, United States Spigen Inc Full time

    SummarySpigen’s HR Sr. Talent Development Specialist designs, develops, processes and facilitates internal and external learning programs to improve organizational effectiveness, support individual development, career mobility, and organizational strengths within brand related teams.Job DutiesCoordinates and facilitates new hire orientation and onboarding...

  • HR Sr. Talent Development Specialist

    1 month ago

    Irvine, United States Spigen Inc Full time

    SummarySpigen’s HR Sr. Talent Development Specialist designs, develops, processes and facilitates internal and external learning programs to improve organizational effectiveness, support individual development, career mobility, and organizational strengths within brand related teams.Job DutiesCoordinates and facilitates new hire orientation and onboarding...

  • Clinical Affairs Specialist

    1 month ago

    Irvine, United States DIALITY INC Full time

    Job DescriptionJob DescriptionJob TitleClinical SpecialistDepartmentClinical AffairsHiring Manager TitleAssociate Director, Clinical AffairsPosition TypeExempt Company & Job Overview:Diality Inc, a privately held medical device company located in Irvine, CA is committed to improving the quality of life for patients with kidney disease. We are developing a...

Sr. Clinical Research Specialist

1 month ago

Irvine, United States Kelly Science, Engineering, Technology & Telecom Full time

Sr. Clinical Research Specialist

(Travel for this role could be 25-40% throughout the US)


Job Summary:

This Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.


Duties & Responsibilities:

  • Serves as a Senior Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones
  • Oversees/executes feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard Operating Procedures
  • May serve as the primary contact for clinical trial sites (e.g. site management);
  • Contributes towards development of clinical trial documents (e.g. study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports)
  • Supports applicable trial registration (e.g. www.clinicaltrials.gov) from study initiation through posting of results and support publications as needed
  • Manages/oversees ordering, tracking, and accountability of investigational devices and trial materials
  • Interfaces and collaborates with site personnel, IRBs/ECs, contractors/vendors, and company personnel
  • Interfaces, collaborates and oversees Clinical Research Associates (CRAs)
  • Oversees and supports the development and execution of Investigator agreements and trial payments
  • Is responsible for clinical data review to prepare data for statistical analyses and publications;
  • May perform monitoring activities including site qualification visits, site initiation visits, interim monitoring visits or close out visits based on study need
  • May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) within the assigned projects
  • May provide on-site procedural protocol compliance and data collection support to the clinical trial sites
  • Contributes to the critical assessment of the literature and to the interpretations and disseminations of all evidence generated
  • Contributes to delivery of assigned clinical projects, through effective partnership with the study core team leading to delivery of clinical project commitments (deliver on time, within budget and in compliance with regulations and SOPs)
  • May development of e Post-Market Clinical Follow-up (PMCF) Plans and PMCF Evaluation Reports (ER) within the defined timelines and review/update at planned intervals; May assist with maintaining the overview to assure (study) commitments are timely and properly met by coordination of specific documentation and contribution to cross-functional review of associated documents where relevant
  • Supports project/study budget activities
  • Mentors team members
  • May perform other duties assigned as needed
  • Is responsible for communicating business related issues or opportunities to next management level. Function as a reliable, trusted resource of accurate, up-to-date project knowledge as requested by key stakeholders
  • Is responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures
  • Should develop a strong understanding of the pipeline, product portfolio and business needs;
  • Generally manages work with supervision, dependent on project complexity. Independent decision-making for simple and more advanced situations but required guidance for complex situations


Education:

  • Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.


Experience:

  • BS with at least 4 years, MS with at least 3 years, PhD with at least 2 years of relevant experience preferred.
  • Previous experience in clinical research or equivalent is required.
  • Relevant industry certifications preferred (i.e., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV,…).
  • Clinical/medical background is a plus.
  • Medical device experience is highly preferred.