CLINICAL RESEARCH ADMINISTRATOR I

General Responsibilities

• To manage intake, triage, assessment and distribution of study materials.
• To collect and process information related to studies.
• To maintain records and documentation.
• To maintain study compliance with institutional requirements.
• To work with sponsors/study team to arrange required trainings and meetings.
• To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations.

Key Duties & Responsibilities

• This position will be responsible for performing pre-award activities for industry and investigator-initiated studies.
• To manage fiscal aspects of contract negotiations, identifying all of the expenses associated with participating in a clinical trial, negotiating budgets, and developing budgets.
• To collaborate to develop clinical trials processes for consistency and compliance with UAB, Federal, State, and applicable regulatory authorities.
• To serve as a liaison to the UAB Office of Sponsored Programs in negotiating contracts and amendments related to the conduct of clinical research activities.
• To assist in preparing, developing, reviewing, and negotiating industry and sponsored research clinical trial budgets for consistency with UAB policies and operating procedures.
• To identify and obtain sufficient funding to successfully execute clinical research, as applicable.

Qualifications

• A high school diploma or GED is required.
• Strong organization and time management skills are preferred.
• Knowledge of clinical trials, clinical trial billing, and invoicing is preferred.
• Relevant work experience with developing and negotiating budgets for proposals/projects in a clinical research environment is preferred.
• OnCore experience is preferred.

Skills

• Organized and a self-starter.
• The ability to work as part of a team is essential.

Pay

Hourly Range: $18.85 - $30.65

Schedule

Day/1st Shift

Benefits

N/A

Application Instructions

Please attach a current resume with this application.