Aptinyx, Inc. Allergan Work Values

Daily Duties at Aptinyx, Inc. Allergan:

Study startup / site selection documentation processing (feasibility, 1572, etc.) Serious Adverse Event (SAE) follow-up and summarization reporting. Investigational meeting coordinating and hosting. Pharmacokinetics data collection and entry. Trial Master File (TMF) creation and management, including upkeep of in-office study file documents. Manage and update various study protocols and study site information on clinicaltrialsgov.com. Quality assured data entry into EDC system and Excel spreadsheets. Oversight of clinical supplies and shipment to various study sites. Assist clinical team with assignments and help maintain workload. Manuscript creation and preparation for investigator meetings, staff training, and site orientation. Administration of filing, faxing, telephones, meeting minutes, stocking, etc.

What they like about Aptinyx, Inc. Allergan:

Working for a company with an emphasis on social values and helping society is a clear and important priority for you - a critical factor in who you choose to work for. In contrast to other factors, you place an organization's reputation for fairness and concern for the community above most other aspects of the company. As you search for a new job opportunity, it is usually possible to find out if the company is involved in the community and/or if it is addressing problems and issues in society. Pay special attention to non-profit organizations and those specifically involved in social action. Moreover, speaking with current and former employees should enlighten you to perceptions of the fairness of the company's leaders and the treatment of employees.

Tags

Clinical, Remote, Data Manager, Researcher, Pharma, Industry, CRO, Specialist, EDC, SAE, TMF, Study Startup

Skills

Communication, Efficient, Motivated

These are some of the questions we asked our climbers about their experiences with Aptinyx, Inc. Allergan: