Clinical Research Coord I

Tanner Clinic; Murray (UT); On-site; USD 30,000 - 45,000; Part time

Job summary

A leading healthcare provider in Murray is seeking a Clinical Research Coordinator to manage clinical trials and coordinate with subjects. The role requires excellent communication, organizational skills, and a background in the medical field. Responsibilities include recruitment, data management, and ensuring compliance with safety standards. This part-time position offers a dynamic work environment with opportunities for professional growth.

Qualifications

• Background in medical field or related courses required.
• Certifications like CCRC, CNA, CMA, LPN preferred.

Responsibilities

• Recruitment and coordination of trial subjects.
• Data collection and management including phlebotomy.
• Coordination and management of clinical trials.

Skills

Communication

Organization

Attention to Detail

Logic and Reasoning

Education

Background in a medical field

College-level human body related courses

Tools

Microsoft Word

Standard office equipment

Medical equipment

Job description

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Description

Tanner Clinic has an immediate opening for a Clinical Research Coordinator.

Job Type

Part-time

Essential Job Responsibilities

• Recruitment and coordination of trial subjects covering informed consent, screening subjects through inclusion and exclusion criteria, and adhering to safety and compliance issues.
• Coordination and management of the clinical trial, generating source documents on Microsoft Word, time management, visit coordination, product dispensing and accountability, managing monitoring visits, and communication with sponsor and authorities.
• Data collection and management, obtaining medical histories and vital signs, performing phlebotomy, lab processing and shipping, recording and management of AEs, completing CRFs, filing and archiving, and resolving queries.
• Other duties as assigned.

Requirements

Education:

• Background in a medical field and/or completed college-level human body related courses.
• Certifications and/or licenses are preferred but not required: CCRC, CNA, CMA, LPN.

Experience

• Previous clinical research experience is preferred but not required.

Other Requirements

• Excellent written and verbal communication skills.
• Highly motivated, organized, and strong attention to detail.

Knowledge

Performance Requirements

• Knowledge of principles and processes for providing customer and personal services, including customer needs assessment, meeting quality standards, and evaluating satisfaction.
• Knowledge of administrative and clerical procedures such as word processing, managing files and records, designing forms, and office terminology.

Skills

• Using logic and reasoning to identify strengths and weaknesses of solutions and approaches.
• Effective written communication tailored to the audience.

Abilities

• Read and understand information presented in writing and conversation.
• Apply general rules to specific problems to produce sensible answers.

Equipment Operated

Standard office equipment (computers, fax, copiers, printers, telephones) and medical equipment (ECG, blood pressure cuffs, centrifuge, phlebotomy tools).

Work Environment

Well-lighted office environment with occasional evening and weekend work.

Mental/Physical Requirements

Sitting approximately 50% of the day, walking or standing the remainder, varying by trial requirements.