Spotlight Employers
Clinical Study Managers
The Clinical Study Manager is responsible for the day-to-day operations for one or multiple clinical trials. The Clinical Study Manager serves as the trial leader and provides direction to the clinical team to support the overall goals and requirements of the clinical site and sponsors. The Clinical Site Manager drives and manages the clinical study by setting the objectives, scope, strategy and schedule, all the while ensuring that all clinical trial processes adhere to Good Clinical Practices as well as other imposed regulations and guidelines.
This is a hands-on role in any clinical site, so a four-year degree in life sciences is required in addition to extensive experience in a clinical research environment. Excellent communication skills are critical as well as a comfort level with discussion and viewing medical procedures.
Employment Outlook
Career opportunities for Clinical Study Managers are found in hospitals, physicians’ offices, contract research organizations, biomedical research organizations and institutions, sectors of the government, and specialty disease centers and pharmaceutical and medical device suppliers. With the rapid growth of the healthcare industry, Clinical Study Manager positions are expected to increase 14% or more in the next 10 years.
Current Job Openings
Clinical Project Manager
Responsibilities
The qualified candidate will be an experienced Clinical Project Manager that is capable of handling...(more)
Clinical Research Manager
Fast growing clinical research organization seeks clinical research manager with at least 4 years of oncology study management experience.
Description -
-Manage interdisciplinary clinical...(more)
Clinical Data Manager
Job Summary
Serves as the primary Kendle CDM contact with Sponsors and represents CDM on project teams. Responsible for project timelines, deliverables, financial...(more)
Drug Safety Associate
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Clinical Data Coder
Job Summary
Serves as a resource primarily for the local Kendle Clinical Data Management (CDM) organization regarding the coding of clinical trials data (i.e. adverse...(more)
Biostatistician
Job Summary
Acts as the Principal statistician for Kendle projects with any complexity. Commonly performs the following activities: assists in marketing and bidding...(more)
Clinical Research Associate (CRA)
Exciting regional home-based permanent opportunity with one of the fastest growing International Clinical Research Organizations in the country. CRA's with 2-3 year of oncology monitoring...(more)
Clinical Research Assistant
Research Assistant Scientist
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Clinical Data Analyst
Responsibilities Include:
- Provide input from the data management perspective regarding the design of clinical trial protocols.
- Design and develop case report forms (CRFs)...(more)
Clinical Data Manager
Sanofi Pasteur in the USA is a leader in the research, development, manufacture, marketing and sales of vaccines and immunological products because here we clearly see a better tomorrow for all...(more)