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Clinical Research Coordinator

Description:Job Summary

The Clinical Research Coordinator will be responsible for assisting the development of research/clinical investigations/studies as well as maintaining and supporting active research studies/protocols. They will also be responsible for providing first-line management of clinical trials, including protocols development, maintaining regulatory documentation and submissions, maintaining research records, and data collection, compilation and management.

Responsibilities and Duties
Investigate the feasibility and contribute to the development of applying a wide variety of scientific methodologies and concepts to potential inventions, products and problems.
Assist with the administrative management of active research protocols as well as contribute to the administration of developing research protocols.
Assist with formulating experimental hypotheses and designs experimental and other study protocols.
Assist in developing necessary new technologies and protocols, processes and interprets experimental and other study data, coordinates with other technical and professional staff.
Assist in the preparation of documents, written reports, and manuscripts, including data collection, management, and analyses, for submission to scientific journals, and completed other projects as needed.

Qualifications and Skills
Education: Minimum of a Bachelor's degree in nursing, or Behavioral Sciences. Master's degree in a related field is desired.
Experience: 3 years of experience within the last 4 years. Prior experience within the DoD/VA systems of care strongly preferred.
License/Certifications: Hold current certifications and related training, such as research ethics and compliance, HIPPA, etc., along with related experiences as a clinical research coordinator.
Shall hold a current BLS through AHA or ARC.

Please send resume to for consideration.
Salary:Depends on Experience
Category: Medical
Location:Destin, FL
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