Clinical Research Manager jobs in Texas

Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)

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Clinical Research Site Manager
  • DM Clinical Research
  • Tomball, TX FULL_TIME
  • Clinical Research Site Manager
    The Site Manager's job is to ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. Also To ensure study enrollment meets or exceeds Sponsors' expectations and company goals are achieved on a timely basis.

    DUTIES & RESPONSIBILITIES
    • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
    • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s).
    • Responsible for immediate supervision and performance of the assigned site staff under the supervision of the Site Director or Director of Site Operations.
    • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
      • Sponsor-provided and IRB-approved Protocol Training
      • All relevant Protocol Amendments Training
      • Any study-specific Manuals Training as applicable
      • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
    • It is the responsibility of the Site Manager to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
    • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow-up on the action items, at their respective sites.
    • Make sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study-related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
    • Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs, and guidance documents.
    • Ensuring data quality, subject retention, and compliance, timely and adequate study data reporting on the assigned protocol(s) being conducted at their respective site(s).
    • Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
    • Coaching, counseling, and disciplining the employees as applicable.
    • To develop, coordinate, and enforce site-specific systems, policies, procedures, and productivity standards.
    • Communicating and effective implementation of strategic goals from senior management to the site team.
    • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
    • Strive to ensure weekly, monthly, and quarterly assigned goals are met for their respective site(s).
    • Being prepared for and available at all required company meetings.
    • Submitting required administrative paperwork per company timelines.
    • Occasionally attending out-of-town Investigator Meetings.
    • Any other matters as assigned by management.
    KNOWLEDGE & EXPERIENCE
    Education:
    • Bachelor’s degree preferred
    • Advanced degree preferred
    Experience:
    • At least 4 years of clinical research coordinator experience, including 2 years of management experience at a clinical research organization.
    Credentials:
    • Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.
    Knowledge and Skills:
    • Solid teamwork, organizational, interpersonal, and problem-solving skills and attention to detail.
    • Critical Thinking
    • Active Listening
    • Reading Comprehension — Understanding written sentences and paragraphs in work-related documents.
    • Speaking and Writing to communicate effectively as appropriate for the needs of the audience.
    • Ability to multitask, adhere to deadlines, and work both independently and cooperatively with interdisciplinary teams.
    • Strong computer skills in relevant software and related clinical systems are required.
    • Comprehensive knowledge of FDA regulations, ICH-Good Clinical Practices (GCP) and ISOs.
  • 16 Days Ago

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Clinical Research Site Manager
  • DM Clinical Research
  • Humble, TX FULL_TIME
  • Clinical Research Site ManagerDepartmentClinical Operations - HumbleEmployment TypeFull-TimeMinimum ExperienceSenior Manager/SupervisorDM Clinical Research, the largest privately-owned research manage...
  • 8 Days Ago

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Clinical Research Site Manager
  • DM Clinical Research
  • Sugar Land, TX FULL_TIME
  • Clinical Research Site ManagerDepartmentClinical Operations - Sugar LandEmployment TypeFull-TimeMinimum ExperienceSenior Manager/SupervisorDM Clinical Research, the largest privately-owned research ma...
  • 1 Month Ago

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Clinical Research Site Operations Manager
  • DM Clinical Research
  • Tomball, TX FULL_TIME
  • Clinical Research Site Operations ManagerThe Site Operations Manager will work as a Site Director to ensure study enrollment meet or exceed Sponsors' expectations, and company goals are achieved on a ...
  • 6 Days Ago

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Manager, Clinical Protocol Administration - Clinical Research
  • Clinical Research - MD Anderson Cancer Center Careers
  • United States, TX FULL_TIME
  • The mission of The University of Texas M. D. Anderson Cancer Center is to eliminate cancer in Texas, the nation, and the world through outstanding programs that integrate patient care, research and pr...
  • 12 Days Ago

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Clinical Data Systems Manager
  • DM Clinical Research
  • Houston, TX FULL_TIME
  • Clinical Data Systems ManagerThis role requires a self-motivated individual with extensive project management skills to join the central services team. Your main tasks will include overseeing clinical...
  • 1 Month Ago

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Clinical Research Manager
  • Triton Medical Robotics
  • Burlingame, CA
  • Triton Medical Robotics, a division of Neptune Medical, is an innovative, venture capital funded medical device startup ...
  • 4/25/2024 12:00:00 AM

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Clinical Research Manager (Clinical Research Regulatory)
  • Thomas Jefferson University
  • Philadelphia, PA
  • Responsibilities The Clinical Research Coordinator IV trains research staff, supervises staff and oversees clinical tria...
  • 4/25/2024 12:00:00 AM

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Clinical Research Manager
  • Colgate-Palmolive
  • Piscataway, NJ
  • No Relocation Assistance Offered # 159181 - Piscataway, New Jersey, United States **Who We Are** Colgate-Palmolive Compa...
  • 4/25/2024 12:00:00 AM

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Clinical Research Manager | General Medicine (Remote)
  • Idaho State Job Bank
  • Boise, ID
  • Clinical Research Manager General Medicine (Remote) at Merck in Boise, Idaho, United States Job Description Job Descript...
  • 4/23/2024 12:00:00 AM

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Clinical Research Manager
  • International Spine Pain & Performance Center
  • Washington, DC
  • The International Spine, Pain & Performance Centeris currentlyseeking an ExperiencedClinical Research Manager! Internati...
  • 4/22/2024 12:00:00 AM

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Clinical Research Manager
  • Triton Medical Robotics
  • Burlingame, CA
  • Triton Medical Robotics, a division of Neptune Medical, is an innovative, venture capital funded medical device startup ...
  • 4/22/2024 12:00:00 AM

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Clinical Research Manager (Ophthalmology)
  • Northwestern University
  • Chicago, IL
  • Department: MED-Ophthalmology Salary/Grade: EXS/7 Job Summary: Oversees the Department of Ophthalmology research program...
  • 4/22/2024 12:00:00 AM

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Clinical Research Manager 182825
  • Medix™
  • We are looking to add a Clinical Research Manager to our growing team. This is a full time onsite position with a compet...
  • 4/21/2024 12:00:00 AM

Texas (/ˈtɛksəs/, locally /ˈtɛksɪz/; Spanish: Texas or Tejas Spanish pronunciation: [ˈtexas] (listen)) is the second largest state in the United States by both area and population. Geographically located in the South Central region of the country, Texas shares borders with the U.S. states of Louisiana to the east, Arkansas to the northeast, Oklahoma to the north, New Mexico to the west, and the Mexican states of Chihuahua, Coahuila, Nuevo León, and Tamaulipas to the southwest, while the Gulf of Mexico is to the southeast. Houston is the most populous city in Texas and the fourth largest in the...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Manager jobs
$97,148 to $128,714

Clinical Research Manager in Richland, WA
Clinical research managers must plan every phase of research programs, from initial concept through product development and clinical trials to submission for approval by the U.S.
November 27, 2019
Clinical Research Manager in Spartanburg, SC
Research is both the foundation and the future of medicine.
December 17, 2019
Clinical Research Manager in Vallejo, CA
When transitioning into the clinical research field from a science background, it is good to know what experience you have, what positions you are interested in, and what careers are most appropriate for your background.
December 19, 2019