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 a Clinical Research Company that specializes in conducting clinical trials and are looking to hire energetic, quick learners with basic medical skills to be a part of our team.
We will provide training for most of the job responsibilities.
The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the Research Director.
The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. The CRC will also work on patient recruitment, general administrative tasks, and data entry.
The Clinical Research Coordinator undertakes the performance of clinical trials. The individual seeking this position will be responsible for all aspects of completion of the research study.
Ideal candidate will possess good verbal and written communication skills, work well independently an ability to adjust and interact with various types of people. Must be a team player, maintain confidentiality, and be comfortable working in the medical field.
Candidate will demonstrate customer service that is compassionate, courteous, friendly, non-judgmental, and demonstrate a respect for privacy.
Previous experience in clinical research is a plus.
CRC duties include, but not limited to:
-Screens for subject eligibility for research protocols; patient recruitment-Maintains records for clinical study and regulatory documents.
-Performs blood work, EKGs/ECGs and other clinical procedures on study participants.
-Coordinates and schedules research subject appointments for tests and procedures.
-Corresponds with research subjects throughout the study
-Obtains, reviews, and records medical history for the subject during the duration of the trial
-Communicates with subjects and/or caregiver regarding medication changes, adverse events, scheduling visits, and study drug compliance.
-Administers scales, diagnostic testing, and other study assessments.
-Composes and types study correspondence and other source documentation
-Collects and enters data into study database
-Perform other tasks as assigned.
Job Type: Full-time
Pay: $18.00 - $22.00 per hour
Expected hours: 40 per week
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Work Location: In person
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