Spotlight Employers
Data Managers
The Clinical Data Manager oversees all aspects of the collected data from a clinical trial. The individual typically works with other clinicians to standardize all data management procedures, including operating procedures for data collection, and ensures the highest quality levels for all collection methods. The Clinical Data Manager also is responsible for the review and approval of all databases and documentation used during the data collection phase.
Due to the related technical complexity and high-profile nature of this role, a Masters/PhD is required in addition to extensive experience in the clinical environment. An in-depth knowledge of database management and software applications related to clinical research is also required.
Employment Outlook
Hospitals, contract research organizations, biomedical research organizations and institutions, specialty disease centers, pharmaceutical and medical device suppliers and sectors of government are all in search of highly skilled and experienced Clinical Data Managers. Due to the healthcare industry’s increasing dependency on technology and software applications to propel and advance data collection and patient care, Clinical Data Manager opportunities are expected to grow 14% or more in the next 10 years. Clinical Data Managers earn an average of $40.00 to $49.50 an hour for an annual salary of $83,200 to $102,960 a year or higher, depending on degrees obtained, the research setting, credentials and experience.
Current Job Openings
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)
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)
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 Research Coordinator (CRC)
Fast growing physicins group seeking seasoned CRC for location 90 miles northeast of Raleigh, NC. Group conducts research across wide variety of therapeutic arenas.
Job Responsibilities...(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 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 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)
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)
Biostatistician
SENIOR BIOSTATISTICIAN
North Wales, PA
Exempt Position
...(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)