Research Assistant at US Digestive Health

Wyomissing, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

24 Aug, 26

Salary

0.0

Posted On

27 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Phlebotomy, Data Verification, Specimen Handling, Patient Recruitment, Case Report Forms, EMR Systems, Microsoft Office, Venipuncture, Quality Control, Regulatory Documentation, Clinical Trial Support, Interpersonal Communication

Industry

Medical Practices

Description

Description Summary/Objective Under general supervision from the Clinical Research Coordinators, the Research Assistant is responsible for aiding with the recruitment, collection, processing, and shipping of samples, specimens, and data. Essential Functions Collect, process, and assist in the compilation and verification of research data, samples, and/or specimens (following strict protocol and detailed instructions) Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol Enter and maintain case report forms per FDA guidelines, and review them against the patient’s medical record for completeness and accuracy Ensure the filing and maintenance of all regulatory documents Assist coordinators with preparation of source documents Assist with subject recruitment and schedule patient visits Provide general office support to keep operations running smoothly Preparing patients for blood draws Collecting blood samples through venipuncture or capillary puncture Labeling and storing blood samples correctly for laboratory analysis. Maintaining equipment and ensuring a clean work environment. Assisting patients who may experience adverse reactions during or after the blood draw. Competencies Comprehensive knowledge of applicable safety and specimen handling guidelines and procedures. Able to effectively present information and respond to questions from physicians, staff and patients Proficiency in Microsoft Office software preferred, knowledge of EMR systems required Able to function effectively in a team setting Must have critical thinking skills Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals Able to demonstrate consistent professional conduct and meticulous attention to detail Must be a self-starter and demonstrate initiative Willingness to learn a must Supervisory Responsibility None Work Environment This job operates in a professional medical office environment, utilizing standard office equipment. Physical Demands The physical demands include standing, walking, and occasionally lifting or moving up to 25 pounds. Position Type/Expected Hours of Work This is a full-time position, with an 8-hour shift Monday through Friday. No weekends are required. Travel None Work Authorization/Security Clearance Must be authorized to work in the US for any employer AAP/EEO Statement US Digestive Health is an Equal Opportunity Employer. USDH does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided based on qualifications, merit, and business need Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities vary dependent on job location. Requirements Education and Experience Minimum of a High School Diploma or GED and a graduate of an accredited phlebotomy program required Phlebotomy certification required Minimum 1-2 years related experience required Previous Medical Assistant preferred Previous experience with clinical trials a plus

Responsibilities

The Research Assistant supports clinical research by recruiting subjects, collecting and processing biological samples, and maintaining accurate research data. They are also responsible for ensuring regulatory document compliance and providing general office support.