Job Description

Job Location: Leawood-Granada - Leawood, KS 66211
Position Type: Full Time
Salary Range: $21.63 - $26.44 Hourly

Duties and Responsibilities (Responsibilities necessary to accomplish job functions)
- Assists coordinators with patient visits including scheduling/tracking, data acquisition/data entry, procedures such as biopsies, administration of photodynamic therapy, adhesive lesional stripping, and related tasks.
- Assists with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol
- Assists physicians with patient care and treatment assisting with instruments, injections, and suture removal
- Collects EKGs and vital signs
- Assists clinical trials coordinator and principal investigator with initiation and maintenance of study protocols
- Assists with study visits per study protocol, inclusive of source document and case report form completion and submission
- Performs laboratory duties and functions related to study protocols.
- Ensured clinical trial files are documented in accordance with company standard operating procedures, study protocol and Good Clinical Practice.
- Reviews exclusion/inclusion criteria with the Principal Investigator or Lead Coordinator to ensure subject eligibility
- Process blood, urine, and biopsy samples in accordance with study protocols and IATA/ OSHA standards
- Stocks and organizes medical supplies in exam rooms as needed. Notify appropriate personnel when supplies are needed
- Screen potential research participants and clinical patients for enrollment
- Working knowledge, at minimum, of all applicable protocols. Some team members may be assigned as the primary coordinator for a specific protocol, and should therefore have in-depth knowledge of that protocol
- Adheres to all safety policies and procedures in performing job duties and responsibilities while supporting a culture of high quality and great customer service.
- Performs other duties that may be necessary or in the best interest of the organization.

QualificationsExperience Requirements
- 4 years / Bachelor’s Degree, includes but not limited to life sciences or social sciences
- Medical assistant or equivalent clinical experience; at least 1 year of experience that is directly related to the duties and responsibilities specified, preferred
Knowledge, Skills and Abilities Requirements
- Meticulously detail oriented, professional attitude, reliable
- Organizational skills to support accurate record-keeping
- Ability to follow verbal & written instructions
- Interpersonal skills to work as a team with patients and outside parties
- Able to communicate effectively in English, both verbally and in writing, with proper grammar and spelling skills to avoid mistakes or misinterpretations
- Mathematical and analytical ability for basic to intermediate problem solving
- Basic to intermediate computer operation
- Proficiency with Microsoft Excel, Word, and Outlook
- Specialty knowledge of systems relating to job function
- Knowledge of state and federal regulations such as ICH GCP, IATA; general understanding of HIPAA guidelines

Supervisory Responsibilities:
- This position has no supervisory responsibilities.
Benefits:
- Medical, Dental, & Vision
- 401k
- PTO & Paid Holidays
- Company Paid Life Insurance
- Employee Perks Program