Clinical Research Manager - Houston, United States - H0114 Vision Sciences

Description

Job Description - Clinical Research Manager (STA014338)

Job DescriptionClinical Research Manager - ( STA Organization Organization :
H0114 Vision SciencesDescriptionOversees investigator-initiated and sponsored clinical research projects.

Manages graduate students, post-doctoral fellows and Clinical Lab staff in providing complex administrative duties to support the study and ensure compliance with regulations.

Manage advertising and recruitment of clinical research subjects within the clinic and the community; conduct phone interviews, answer questions regarding ongoing studies, screen, and consent and enroll study subjects.

Track study recruitment, enrollment, drop out, and screen failure rates.
Schedule study visits and provide visit reminders.
Participate in site qualification/initiation/close-out and other study-specific training.
Perform limited study procedures with appropriate training; including questionnaires, automated machinery and vision testing.
Assist with preparation of all IRB and Regulatory documents including but not limited to trial registrations and sponsor reports.

Maintain accurate source documentation and appropriate forms including participant records, drug documentation, reconciling study drug accountability; monitors documentation for quality and accuracy.

Ensure research studies are conducted in accordance with Good Clinical Practice (GCP) guidelines and requirements of the University of Houston and study sponsors.

Maintain licensure and certification records for all study personnel.
Resolve data queries with study sponsors. Maintain supply inventory (general office and lab) and coordinate maintenance and calibration of equipment. Establish effective, collaborative working relationships with clinicians, patients, and sponsors. Provide additional support and guidance for graduate students involved in research. Performs other job-related duties as required.

Manage advertising and recruitment of clinical research subjects within the clinic and the community; conduct phone interviews, answer questions regarding ongoing studies, screen, and consent and enroll study subjects.

Track study recruitment, enrollment, drop out, and screen failure rates.
Schedule study visits and provide visit reminders.
Participate in site qualification/initiation/close-out and other study-specific training.
Perform limited study procedures with appropriate training; including questionnaires, automated machinery and vision testing.
Assist with preparation of all IRB and Regulatory documents including but not limited to trial registrations and sponsor reports.

Maintain accurate source documentation and appropriate forms including participant records, drug documentation, reconciling study drug accountability; monitors documentation for quality and accuracy.

Ensure research studies are conducted in accordance with Good Clinical Practice (GCP) guidelines and requirements of the University of Houston and study sponsors.

Maintain licensure and certification records for all study personnel.
Resolve data queries with study sponsors. Maintain supply inventory (general office and lab) and coordinate maintenance and calibration of equipment. Establish effective, collaborative working relationships with clinicians, patients, and sponsors. Provide additional support and guidance for graduate students involved in research. Performs other job-related duties as required.

EEO/AAStandard AttachmentsCandidates interested in applying for the position must submit the following documents with the application:
Cover letter describing the manner in which your experience applies to the posting.
ResumeSalary History (list Employer name, dates, and last salary)Three work references, including current and past supervisors.


NOTE:
We will maintain your confidentiality and notify you in advance of making contact with any of your references. References will be contacted only after the interviewing process has been completed.

Qualifications Bachelors and 5 years experienceRequires a thorough understanding of both theoretical and practical aspects of an analytical, technical or professional discipline; or the basic knowledge of more than one professional discipline.

Knowledge of the discipline is normally obtained through a formal, directly job-related 4 year degree from a college or university or an equivalent in-depth specialized training program that is directly Requires a minimum of five (5) year of directly job-related experience.

Additional Job Posting Information:
Department is willing to accept experience in lieu of educationDepartment is willing to accept education in lieu of experienceThe candidate should have the ability to perform informed consent of research subjects, oversee regulatory/IRB compliance, manage procurement/financial documentation, develop SOPs, write basic protocols and other IRB documents (e.g. consents, recruitment materials, etc.)

with minimal supervisionSalary :

Commensurate with experience Required Attachments by Candidate : Resume, Cover Letter/Letter of ApplicationEmployee Status Job Posting Job Posting : Mar 28, 2024, 7:40:12 PMThe policy of the University of Houston System and its universities is to ensure equal opportunity in all its educational programs and activities, and all terms and conditions of employment without regard to age, race, color, disability, religion, national origin, ethnicity, military status, genetic information, sex (including gender and pregnancy), sexual orientation, gender identity or status, or gender expression, except where such a distinction is required by law.

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