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 Data Manager
As part of a clinical working group, the Sr. Clinical Data Manager (CDM) is responsible for the accuracy and completeness of the clinical data collected during a clinical...(more)
Biostatistician
Position Title: Biostatistician II
Working Location: Durham, North Carolina
Employment Status: Full-Time Regular
Required Experience: 2 years
Required Education: Masters...(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)
Medical Writer
Job Summary
The medical writer in Regulatory Services is responsible for assisting the Senior medical writer in managing the effective and efficient utilization of...(more)
Clinical Project Manager
Responsibilities
The qualified candidate will be an experienced Clinical Project Manager that is capable of handling...(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)
Regulatory Affairs Associate
Job Summary
The Associate Director Clinical Regulatory, is responsible for the effective and efficient utilization of regulatory personnel and resources related to the...(more)
Clinical Research Associate (CRA)
Clinical Research Associate
Description:
Assists in the design, planning, and implementation of clinical research projects. Coordinates activities between company, Contract...(more)
Clinical Research Associate (CRA)
Title: Clinical Research Associate
Country United States
Description
- Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 - 50% travel) for GCP...(more)
Clinical Research Associate (CRA)
- Conducts site monitoring of clinical research studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP.
- Provide clinical...(more)