Iterative Health is looking to solve the problem of accelerating clinical research to transform patient outcomes in the field of gastrointestinal (GI) and hepatology novel therapies.
Requirements
- CRC certification preferred.
- Knowledge of grammar, spelling, and punctuation.
- Knowledge of purchasing, budgeting, and inventory control.
- Skill in taking and transcribing dictation and operating office equipment.
- Skill in answering the phone and responding to questions.
- Ability to competently use Microsoft Office, including Word, PowerPoint, Excel, and appropriate practice management software.
- Minimum 4 or more years of clinical research experience.
Responsibilities
- Communicate study requirements to all individuals involved in the study.
- Develop and implement recruitment strategies in accordance with Impact Research and IRB requirements and approvals.
- Screen subjects for eligibility using protocol specific inclusion and exclusion criteria.
- Entry of participant information and study visit procedures into the Clinical Trial Management System to ensure billing to appropriate funding source.
- Maintains adequate inventory of study supplies.
- Complete study documentation and maintenance of study files in accordance with sponsor requirements and Impact Research policies and procedures.
- Manage the day to day activities of the study including problem solving, communication and protocol management.
Other
- High school diploma/GED certificate required.
- Associates degree from an accredited university preferred.
- Must be able to lift up to 25 lbs.
- Must be able to travel and MVR
- Ability to work under pressure, communicate and present information.
