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 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)
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)
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)
Biostatistician
The Biostatistician Acts as lead statistician on projects of moderate to large size and complexity; support lead statistician on very large, complex studies. May have staff management and/or...(more)
Clinical Project Manager
Responsibilities
The qualified candidate will be an experienced Clinical Project Manager that is capable of handling...(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)
Drug Safety Associate
- Assist with the overall Clinical Safety and/or Pharmacovigilance operations associated with products including the entire adverse events process: which may include...(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)
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 Project Manager
Responsibilities
CLINICAL PROJECT MANAGER
The successful candidate will be responsible for...(more)