Clinical Research Manager jobs in Houston, TX

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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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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Senior Manager of Enrollment and Clinical Strategy
  • DM Clinical Research
  • Houston, TX FULL_TIME
  • Senior Manager of Enrollment and Clinical Strategy The Senior Manager of Enrollment and Clinical Strategy is responsible for leading the enrollment success vertical implementing new initiatives, impro...
  • 1 Month Ago

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0 Clinical Research Manager jobs found in Houston, TX area

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Principal Scientist
  • Bausch + Lomb
  • Houston, TX
  • Bausch + Lomb (NYSE/TSX: BLCO) is a leading global eye health company dedicated to protecting and enhancing the gift of ...
  • 4/24/2024 12:00:00 AM

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Institute Associate Scientist III -ADME/PK
  • MD Anderson Cancer Center
  • Houston, TX
  • MD Anderson is known for providing cancer patients with exceptional care, which includes early access to innovative new ...
  • 4/24/2024 12:00:00 AM

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Institute Associate Scientist II - Translational Biology
  • MD Anderson Cancer Center
  • Houston, TX
  • MD ANDERSON THERAPEUTICS DISCOVERY DIVISION Within The University of Texas MD Anderson Cancer Center lies a powerful eng...
  • 4/24/2024 12:00:00 AM

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Research Assistant I - MS, Cardiothoracic Vascular Surgery Research Division
  • UT Health Science Center at Houston
  • Houston, TX
  • Cardiothoracic Vascular Surgery Research Division, full time, nonexempt position. Will be supporting the Cardiothoracic ...
  • 4/24/2024 12:00:00 AM

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Clinical Research Scientist, GI Med Oncology - Research
  • University of Texas M.D. Anderson
  • Houston, TX
  • The primary purpose of the Clinical Research Scientist is to assist in the interrogation of large datasets, development ...
  • 4/24/2024 12:00:00 AM

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Research Data Coordinator Lymphoma-Myeloma - Research - No Experience Required
  • MD Anderson
  • Houston, TX
  • The primary purpose of this position is to provide exceptional patient-facing research care for the Lymphoma Observation...
  • 4/24/2024 12:00:00 AM

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Research Data Coordinator Lymphoma-Myeloma - Research - No Experience Required
  • University of Texas M.D. Anderson
  • Houston, TX
  • The primary purpose of this position is to provide exceptional patient-facing research care for the Lymphoma Observation...
  • 4/24/2024 12:00:00 AM

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Coordinator, Research Data - Head & Neck Surgery
  • University Of Texas Md Anderson Cancer Center
  • Houston, TX
  • The University of Texas MD Anderson Cancer Center in Houston is one of the world's most respected centers focused on can...
  • 4/23/2024 12:00:00 AM

Houston is located 165 miles (266 km) east of Austin, 88 miles (142 km) west of the Louisiana border, and 250 miles (400 km) south of Dallas. The city has a total area of 627 square miles (1,620 km2); this comprises 599.59 square miles (1,552.9 km2) of land and 22.3 square miles (58 km2) covered by water. The Piney Woods are north of Houston. Most of Houston is located on the gulf coastal plain, and its vegetation is classified as temperate grassland and forest. Much of the city was built on forested land, marshes, swamp, or prairie and are all still visible in surrounding areas.[citation need...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Manager jobs
$99,530 to $131,870
Houston, Texas area prices
were up 2.3% from a year ago

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