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Title:  Senior Regulatory Affairs Associate

Division:  Pediatrics
Schedule:  Monday - Friday, 8:00 a.m. - 5:00 p.m.
Work Location:  Houston, TX
Salary Range:  $77,029 - $98,000
FLSA Status:  Exempt
Requisition ID:  8558

Summary

The Senior Regulatory Affairs Associate works to support the Protocol Office and investigators associated with The Texas Children's Cancer and Hematology Centers (TXCH). This position supports all aspects of regulatory compliance for a specified portfolio of clinical trials. This support includes, but is not limited to, reviewing protocols and protocol related documents, submitting protocols to regulatory agencies and review committees and ensuring successful navigation of approval processes for clinical research. This position requires an understanding of clinical research and applicable regulations.

Job Duties

  • Assigned the most complex studies. These are the studies with IND filings, requires significant prior regulatory experience with Oncology studies and is instrumental in ensuring ongoing study compliance (from a regulatory perspective). This role is highly independent with little direction from the supervisor but lots of experience to drive their work.
  • Independently complete and coordinate regulatory correspondence across internal stakeholders and external institutions. In close collaboration with the Investigator, provide protocol feedback, prepare protocol documents and required regulatory forms in order to obtain institutional and regulatory agency approval for the conduct of clinical research projects at the TXCH.
  • Assist in training junior staff on the team and serves as a resource to staff for general regulatory guidance.
  • Work with the Director to provide input on SOP revisions and adopting required regulatory changes.
  • Maintain and expand understanding of federal regulations, ICH GCP guidelines and internal SOPs by producing work in compliance with those regulations, guidelines and SOPs.
  • Act as a liaison between institutional review committees, regulatory agencies and the investigators to ensure that protocols obtain applicable approvals, that protocol amendments are submitted appropriately and that annual renewals are obtained.
  • Work closely with the study team, research staff, and investigators to assure that all regulatory documents for the research studies are up-to-date.
  • Facilitate communication with IRB and other applicable agencies related to Adverse Events and Unanticipated Problems reporting.
  • Assure distribution of appropriate information between investigators, regulatory agencies and staff involved in implementation of research projects.
  • Maintain regulatory database as applicable.
  • Maintain electronic and paper study files in accordance with local SOPs, sponsor and general industry standards ensuring documentation is complete, up to date, and audit ready.
  • Keep the study team and supervisor informed of protocol related issues.
  • Practice a high level of integrity and honesty in maintaining confidentiality.
  • Work proactively and collaboratively with other team members to streamline work and achieve mutual goals.
  • Attend all required meetings, contributes pertinent protocol information and uses information presented to develop an understanding of the hematology/oncology landscape, in order to more accurately assist in the preparation of submissions.
  • Plan and pursue activities to promote self development related to hematology/oncology and regulatory issues.

Minimum Qualifications

  • Bachelor's degree.
  • Four years of relevant experience.

Preferred Qualifications

  • Four or more years of experience in regulatory affairs and/or clinical research at academic medical center or hospital with knowledge of clinical research practices and regulations
  • Experience in regulatory affairs for clinical research
  • Certification in Clinical Research, SOCRA or other  
  • Knowledge and understanding of clinical research compliance, including OHRP, FDA and other federal regulations and requirements regarding human subjects research, including but not limited to GCPs and related ICH guidelines, informed consent, adverse event reporting and monitoring, and other human subjects research protection requirements
  • Ability to serve as a resource to clinical investigators and staff
  • Ability to manage shifting priorities in short time frames
  • Must have excellent oral and written communication skills
  • Knowledge of medical/scientific terminology 
  • Excellent organization skills; ability to multi-task
  • Strong computer skills including Microsoft Office Suite
  • High sense of professional behavior and conduct and an ability to communicate with various levels of faculty and staff within Baylor College of Medicine and outside organizations
  • Knowledge of clinical research and/or regulatory processes and the applicable federal regulations and ICH GCP guidelines

 

 

 

 

Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.

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