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
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)
Medical Writer
Desription: The Senior Medical Writer will be responsible for reviewing and preparing...(more)
Biostatistician
SENIOR BIOSTATISTICIAN
North Wales, PA
Exempt Position
...(more)
Clinical Data Manager
Bioforce Solution\'s client is looking for a Senior Clinical Data Manager to work on a 6-month contract assignment.
Responsibilities:
The Contract Senior Clinical Data Manager will be...(more)
Clinical Research Associate (CRA)
The Clinical Research Associate II performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of...(more)
Clinical Project Manager
Successful candidate will conduct the clinical trial project from the data management perspective according to approved Data Management Working Practices (WPD's) and SOPs. Will coordinate and...(more)
Clinical Financial Analyst
Under general direction, responsible for the production of timely and accurate financial reports for internal and external reporting purposes. Assist in preparation of work papers for the...(more)
Clinical Data Analyst
Responsible for various special projects related the data management aspects of clinical studies. Interface with data management and systems development groups.
Primary...(more)
Clinical Data Programmer
Successful candidate will work as part of a project team, or possibly as a team manager, to design and implement applications in support of clinical research and biostatistics. Candidate will...(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)