Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
We are seeking a Per Diem Clinical Assistant II for our growing organization!
Responsibilities include, but are not limited to:
Minimum High school diploma, but bachelor’s degree preferred. Minimum 2 years relevant work experience in clinical research or health related environment. Strong clinical skillset is required (blood draws, EKGs, vitals). Ability to follow general guidance and direction in accordance with FDA regulations and GCP/ICH guidelines as they apply to the conduct of clinical research. Strong interpersonal, written and verbal communication skills are required. Able to read, understand and build knowledge of study instructions, protocols and procedures. Ability to convey courtesy and empathy for subjects/patients. Excellent organizational skills. Attention to detail. Consistency in meeting deadlines. Familiarity and comfort in learning Microsoft Office Suite and related application software. Able to work assigned study schedules, as determined by clinical study demands and TKL business needs and priorities. This is a per diem position based primarily in our Fair Lawn, NJ office. Shifts typically run from 7pm-11pm, 11pm-7am, or 7pm-7am. Primary need is Friday, Saturday, and Sunday nights.
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