Discovery Clinical Trials Work Values

Daily Duties at Discovery Clinical Trials:

Follow established guidelines in the collection of clinical data and/or administration of endocrinology studies. Assist in preparation and submission of essential documents for submission to Sponsor and/or IRB for regulatory filing purposes and maintenance. Confer and recruit potential study subjects to explain purpose of study and obtain informed consent; explain diagnostic procedures and/or treatment plans to alleviate subject and/or family concerns. Schedule subjects for study and laboratory procedures as well as treatments based on protocol instructions. Conduct subject study visits according to protocol timelines and perform any procedures. Ensure all protocol required blood samples, cultures, tissues, and other specimens are obtained for laboratory analysis. Ensure all laboratory specimens are processed and shipped according to laboratory instructions and within specified timelines. Dispense study drug to qualified study subjects and perform drug accountability on all returned study drug. Collect data from subject charts, medical records, interviews, questionnaires, diaries, diagnostic tests, and other sources and transcribe to Case Report Forms (CRFs) or perform Remote Data Entry (RDE). Obtain patient consent forms; schedule research visits and phlebotomy; and input research data and case reports into applicable database.

What they like about Discovery Clinical Trials:

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

Oncology, Monitoring, Endocrinology, EDC, Inform, Medidata, IWRS, In house monitoring, QA, IRB, Regulatory Submission, CTMS, Clinphone

Skills

IRB submission, EDC expertise , QA studies, Supervise other CRCs, Endocrinology, Oncology, Lab Processing, CTMS, Microsoft Excel, Microsoft Word, Microsoft Powerpoint, Microsoft Outlook, Phlebotomy, Medical Terminology, Subject Recruitment

These are some of the questions we asked our climbers about their experiences with Discovery Clinical Trials: