Scientist - Clinical Research assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Being a Scientist - Clinical Research secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Additionally, Scientist - Clinical Research interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. The Scientist - Clinical Research work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Scientist - Clinical Research typically requires 4 -7 years of related experience. (Copyright 2024 Salary.com)
About us
JMG Development Corporation is a small business in North Massapequa, NY. We are professional, agile, professional and our goal is to Hire an assistant to help with a variety of clinical research tasks, including filing, confirming patient appointments, organizing, labeling, learning how clinical trials operate..
Our work environment includes:
Job Summary: We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a crucial role in the planning, coordination, and execution of clinical trials. You will be responsible for ensuring compliance with study protocols, collecting and analyzing data, and assisting with the overall management of research projects. Duties: - Assist in the design and implementation of clinical trials - Coordinate and monitor study activities to ensure compliance with protocols and regulatory requirements - Collect, record, and analyze data from clinical trials - Prepare study documentation, including informed consent forms and case report forms - Collaborate with investigators, sponsors, and other stakeholders to ensure smooth study operations - Conduct site visits to monitor study progress and ensure adherence to protocols - Assist with the preparation of study reports and presentations - Maintain accurate and up-to-date study records Skills: - Proficiency in R or other statistical analysis software - Experience working in a research laboratory setting - Knowledge of protein purification techniques - Familiarity with clinical trial processes and regulations - Experience with flow cytometry, chromatography, mammalian cell culture, microscopy, animal physiology, and Western blotting techniques is highly desirable - Strong attention to detail and ability to accurately collect and analyze data - Excellent organizational skills and ability to manage multiple tasks simultaneously - Effective communication skills, both written and verbal We offer competitive compensation packages based on qualifications and experience. This is a full-time position with opportunities for career growth within our organization. Note: All positions must be paid including internship positions.
Job Type: Full-time
Pay: $35,000.00 - $42,500.00 per year
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Work Location: In person
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