Research Coordinator

The
** Research Coordinator
** will screen, enroll, and follow study subjects for Phase I, II, III, and IV clinical trials, ensuring protocol compliance and close monitoring while the subjects are on study.
Review with the Principal Investigator (PI) the inclusion/exclusion criteria, overall structure, and requirements of each protocol and ensure logistics for site implementation. Perform delegated Protocol specific tasks as assigned by Principal Investigator.  Assess and document subject compliance and accountability with Investigational Product (IP). Document re-education when appropriate. Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this job.

Duties, responsibilities, and activities may change at any time, with or without notice.
*
* Qualifications:

** Minimum of two (2) years of clinical research experience.

** Knowledge, Competencies &

Skills:

** Exceptional customer service skills.

Strong attention to detail, a willingness to learn & the ability to stay organized.

Ability to perform clinical assessments.

Proficient knowledge of medical terminology.

Proficient knowledge of Research-related Terminology.

Strong communication skills, both verbal & written.

Proficient computer software and database skills.

Ability to type a minimum of 40 words per minute.

Actual compensation offered to candidates is based on work experience, education, skill level, and geographic location. Compensation may vary depending on the state or region in which the position is located, in accordance with applicable laws.
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