Institutional Research Director - Assistant assists in directing and overseeing institutional research for a university/college. Designs and leads institutional research studies evaluating the effectiveness of the organization's programs and policies. Being an Institutional Research Director - Assistant manages data collection and analysis and oversees the formulation of research reports. Requires a bachelor's degree. Additionally, Institutional Research Director - Assistant typically reports to Institutional Research Director. The Institutional Research Director - Assistant typically manages through subordinate managers and professionals in larger groups of moderate complexity. Provides input to strategic decisions that affect the functional area of responsibility. May give input into developing the budget. Capable of resolving escalated issues arising from operations and requiring coordination with other departments. To be an Institutional Research Director - Assistant typically requires 3+ years of managerial experience. (Copyright 2024 Salary.com)
Description:
The Research Assistant (RA) position delivers a strong customer experience for both sites and patients by providing virtual study support under the delegation of a PI. The RA is accountable for study delivery at the patient level and is expected to support the patient experience, data management, and other study administrative tasks with a quality-first approach. This is an early-to-mid experience position with the expectation that the RA has working knowledge of and experience in the clinical research industry. This role will perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. This position is an onsite part time, hourly role with approximately 24 hours a week.
Skills:
Clinical research, Clinical trial, Pre-screening patients, EDC
Top Skills Details:
Clinical research,Clinical trial
Additional Skills & Qualifications:
· Data extraction from source documents and assist CRC with query resolution
· Basic knowledge of clinical trials and medical terminology
· In-depth understanding of departmental, protocol, and study-specific procedures
· Proficiency in MS Windows and Office applications (Access, Outlook, Excel, Word)
· Excellent interpersonal and communication skills
· Strong attention to detail and ability to work independently.
· Adaptability to a fast-paced environment
· Familiarity with medical and research terminology
· Knowledge of federal regulations and Good Clinical Practices (GCP)
· Critical thinking and problem-solving abilities
· Customer-centric personality with a positive attitude under pressure
· Contribution to team and site goals
· High level of self-motivation
· Optimistic "can-do" attitude
· Willingness to work onsite
Certifications/Licenses, Education, and Experience:
· A minimum of 1-2 years clinical research experience.
· Clinical Research experience required.
Experience Level:
Intermediate Level
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