Spotlight Employers
Clinical Project Managers
A Clinical Project Manager serves as the main point of contact during a clinical trial. The Clinical Program Manager works very closely with other clinicians and is responsible for ensuring that a clinical trial is properly designed and implemented and that the resulting data is properly collected, stored and analyzed. It is also the responsibility of the Clinical Program Manager to ensure that the trial is completed successfully on time within set budget parameters. This role also requires a continuous attention to process flow and a keen eye toward identifying and making improvements to existing processes and procedures.
Because Clinical Project Managers must liaison with so many other roles in a high profile manner, they must possess excellent communication skills. A four-year degree is required; additionally, nursing experience and clinical experience is often required.
Employment Outlook
Career opportunities for Clinical Project Managers typically exist in hospitals, physicians’ offices, contract research organizations, biomedical research organizations and institutions, specialty disease centers and pharmaceutical and medical device suppliers. Positions in this line of work are expected to increase 20% or more in the next 10 years. Clinical Project Managers earn an average of $30.00 to $48.00 an hour for an annual salary of $63,000 to $100,000 or higher, depending on educational degrees obtained, the research setting, credentials and experience.
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)
Clinical Research Coordinator (CRC)
Job Summary-
The Research Nurse Coordinator manages clinical research projects for Principal Investigator via study protocol within the University, competently performs the nursing...(more)
Clinical Research Associate (CRA)
We are a growing EastBay biopharmaceutical company focusing on Oncology drugs. We are currently seeking a Sr. Clinical Research Associate / Sr. CRA to oversee and manage our Phase 1-3...(more)
Clinical Data Manager
:
Under general supervision, the Clinical Data Manager reviews data; assists in database design and testing; designs CRFs and guidelines; designs and tests logic checks;...(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)
Biostatistician
Position Title: Biostatistician II
Working Location: Durham, North Carolina
Employment Status: Full-Time Regular
Required Experience: 2 years
Required Education: Masters...(more)
Medical Writer
Desription: The Senior Medical Writer will be responsible for reviewing and preparing...(more)
Clinical Research Associate (CRA)
This position performs and coordinates all aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products...(more)
Clinical Project Manager
Title: Clinical Trials Project Manager
General Summary:
The Clinical Trials Project Manager will report to and work closely with the Project Director in the coordination and management of...(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)