Clinical Research Assistant (103648)

U.S. Dermatology Partners•Phoenix, AZ

17d•$21 - $25•Onsite

About The Position

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. Ensures 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. Processes blood, urine, and biopsy samples in accordance with study protocols and IATA/OSHA standards. Stocks and organizes medical supplies in exam rooms as needed. Notifies appropriate personnel when supplies are needed. Screens 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.

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
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

Nice To Haves

at least 1 year of experience that is directly related to the duties and responsibilities specified, preferred

Responsibilities

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.
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.