Position Title: Clinical Research Associate III
Work Location: GA, FL, TX, CA 
Assignment Duration: 12 Months

Must have minimum 3yrs monitoring experience with one year or more obesity monitoring experience and prefer prior contracting experience. Will consider candidates with strong endocrinology monitoring experience (2+ yrs endocrinology monitoring).

Description:
Summary:
The main function of a Clinical Researcher is to work as an integral member of the site staff, maintaining the day-to-day relationship with partner sites. Such work involves planning, coordinating, and, as appropriate, execution of clinical studies in accordance with the protocol, contracted scope of work, SOP's, and any relevant local guidelines and regulations.
 
Job Responsibilities:

• Work directly at patient/subject interface at investigator sites to deliver high-quality patient data in accordance with local regulations, agreed scope of work, and as required by protocol.
• Facilitate the timely start-up of all studies at the site by ensuring the timely completion/submission of regulatory documents, ethics approvals, and IP release documents.
• Attend and participate in investigator meetings, monitoring visits, audits, seminars, and other regional or national meetings. Assist with screening and enrollment of subjects into assigned studies.
• Support subjects on trials to encourage maximum retention and future recruitment.
• Assist with the establishment of a recruitment and contingency plan for each study. Perform functions necessary for successful completion of all protocol-required visits/procedures, such as vital signs, phlebotomy, diagnostic tests, dispensing of investigational product, scheduling, drug accountability/reconciliation, and organizational tasks, where appropriate and as delegated by the investigator, in accordance with local country requirements.
• Accurately complete source documents and case report forms in both paper and electronic format.
• Assist the investigator with recording and reporting of adverse events as per local regulatory authority guidelines.
• Ensure documentation of data protection agreement is on file for the assigned site, where necessary, and in accordance with local country requirements.

 Skills:

• Good knowledge of medical terminology.
• Above-average interpersonal and organizational skills.
• Proficient use of Microsoft Office. Fluent in the local language, spoken and written. Fluent in the written English language.
• Ability to work independently, prioritize actively, seek input, problem solve, and work in a team environment.
• Ability to maintain confidentiality. Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

 Education/Experience:

• Registered nurse, medical physician, or appropriate educational qualification; AND

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 55.00/hr.