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Houston Methodist ACM Regltry Complnc Specialist in Houston, Texas

JOB SUMMARY

Coordinate and perform study specific regulatory processes across multiple studies of different therapeutic areas and phases in accordance to appropriate regulations, Standard Operating Procedures (SOP'S), and study specific protocols/plans and processes under the direct supervision of the Regulatory Compliance Manager.

PATIENT AGE GROUP SERVED

Not Applicable

DUTIES AND RESPONSIBILITIES

  • Assure compliance of general and study-specific regulatory and/or safety related processes with SOP's, FDA, GCP, NIH and applicable regulations.

  • Responsible

  • for

  • assisting in the preparation of research protocols for IRB submission, submitting protocol amendments, preparing renewals, preparing necessary regulatory documents for submission to study sponsors, submits adverse event reports, submits safety reports, and notifies IRB of study closures.

  • Build

and

maintain effective relationships with key study personnel.

  • Provide routine updates and reporting to the Regulatory Compliance Manager to ensure timely communication regarding status of regulatory and/or important safety related issues.

  • Act as a liaison between the institutional review committees, regulatory agencies, and the investigators to ensure that protocols are approved and that supplementary information is provided in a timely fashion as requested.

  • Maintain the required regulatory files for all clinical trials to ensure regulatory compliance. Meet with study monitors. Maintain archived documents on and off site.

  • Prepare and manage FDA documents required to initiate investigational drugs trials.

  • May interface with appropriate governmental agency on project/products as identified by the Manager. Assist in the preparation of periodic reports for FDA.

Maintain a professional and credible image with FDA and other regulatory agencies, Sponsors, vendors, patients and co-workers.

Develop appropriate regulatory reports and associated documentation in accordance with SOPs and study specific processes under the direct supervision of the Regulatory Compliance Manager.

Maintains accountability for own ongoing professional growth and development.

Displays ICARE values.

Perform other duties as assigned.

EDUCATION REQUIREMENTS

Bachelor's degree or 30 hours college coursework preferred

EXPERIENCE REQUIREMENTS

3 year relevant research program experience

CERTIFICATES, LICENSES AND REGISTRATIONS REQUIRED

RAPS, CCRC, or CCRP is preferred.

SPECIAL KNOWLEDGE, SKILLS AND ABILITIES REQUIRED

  • Working knowledge of FDA regulations and GCP guidelines.

  • Excellent written and oral communication skills.

  • Ability to multi-task.

  • Organizational skills and attention to detail.

  • Critical thinking ability.

  • Strong analytical skills.

  • Document management skills.

  • Proficient computer skills.

Houston Methodist Research Institute was formed in 2004 to rapidly and efficiently translate discoveries made in the laboratory and the clinic into new diagnostics, therapies, and treatments. The research institute was created to provide the infrastructure and support for these endeavors, and to house the technology and resources needed to make innovative breakthroughs in important areas of human disease. A 540,000 square foot building dedicated to research, the research institute houses over 1,500 staff and trainees, 284 principal investigators and has more than 570 ongoing clinical trials.

Street: 6550 Fannin St.

Name: Cancer Clinical Trials

Regular Shift: 1st - Day

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