Spotlight EmployersSoliant Health

 

Health Direction

Clinical Programmers

Clinical Programming marries the disciplines of healthcare, technology and information systems into one comprehensive role. The Clinical Programmer works closely with a research team to design clinical trials. Subsequently, the Clinical Programmer must not only possess knowledge of clinical data collection procedures; he or she must also be proficient in various software applications and programming methods and possess excellent communication skills. The Clinical Programmer must ensure that systems are designed to accurately collect and process data and be able to quickly identify and troubleshoot issues that might impact patient care. This role must be able to design and build testing methods and collaborate with other clinicians while simultaneously working within technological parameters that may exist in the given work environment.

 

A four-year degree is required for entry into this field; a Masters degree or higher is required at higher, and more independent, levels.

 

Employment Outlook

The future is bright for Clinical Programmers. 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 Programmers. Due to the healthcare industry’s increasing dependency on technology and software applications to propel and advance data collection and patient care, Clinical Programming Analysts opportunities are expected to grow 14% or more in the next 10 years.

 

Current Job Openings

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)

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)

Biostatistician
Position Title: Biostatistician II Working Location: Durham, North Carolina Employment Status: Full-Time Regular Required Experience: 2 years Required Education: Masters...(more)

Clinical Data Analyst
Responsibilities Include:   - Provide input from the data management perspective regarding   the design of clinical trial protocols. - Design and develop case report forms (CRFs)...(more)

Clinical Project Manager
Responsibilities The qualified candidate will be an experienced Clinical Project Manager that is capable of handling...(more)

Clinical Project Manager
Responsibilities CLINICAL PROJECT MANAGER The successful candidate will be responsible for...(more)

Drug Safety Associate
MD (physician) - Medical Affairs / Safety Specialist Description - -medical monitoring -Pharmacoviglance -Writing safety standards -Writing narratives on...(more)

Clinical Data Manager
Minimum Qualifications :   - Five years of experience OR the equivalent combination of education and experience with a...(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)

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)

 

First Name:
Last Name:
Phone:
Email:
Discipline:
Specialty:

© 2008 Clinical Research Jobs. All Rights Reserved. Terms of Use   |   Privacy Policy