Clinical Research Assistant
Full job description
Position Title
Clinical Research Assistant
Work Location
Weslaco, TX
Salary Range
$10-18/hr, based on experience
Schedule
Full-time Non-Exempt Status
Approximate Hours: Mon-Fri 7:00 am – 4:00 pm
Occasional weekend obligations for special projects or meetings
Required Qualifications
Highschool Diploma
Bi-lingual (Spanish/English)
Required Training
Certifications may be completed upon employment
CITI GCP – 3-year renewal
IATA/Hazardous shipping – 2-year renewal
Infection control/ Blood Borne Pathogens – annual renewal
CPR/AED 2-year renewal
CSSR-S (Columbia Suicide Severity Rating Scale)
Required Skills/Abilities
Self-motivated and comfortable accepting feedback and guidance from colleagues
Work well in a team and have excellent oral communication skills
Possess a positive, friendly, and professional demeanor
Proficient with Microsoft Office and general office equipment
Attention to detail
Professional appearance and disposition
Ability to multi-task and manage time effectively in a fast-paced environment
Preferred Skills/Abilities
College student
Experience in the medical profession
Reports To
Lead Clinical Research Coordinator
Position Statement
The mission of all staff at Texas Valley Clinical Research (TVCR) is to conduct ethical clinical research that results in medical advances that improve human health while treating participants with dignity and compassion. TVCR exists to produce clear and concise data for our sponsors while helping community members achieve their healthcare goals. Primary Therapeutic Areas of Interest include, but are not limited to, diabetes, obesity, thyroid disorders, liver or kidney impairment, cardiovascular disease, and Alzheimer's Disease. The Clinical Research Coordinator (CRC) is responsible for conducting phases II – V clinical trials under ICH-GCP guidelines and study protocol standards provided by the study sponsor. A successful research assistant possesses excellent time management skills, works independently, and can follow instructions. Texas Valley Clinical Research's organizational culture is exceptional, characterized by a strong emphasis on teamwork, a love of learning, and a genuine commitment to helping employees reach their professional goals. Supportive, collaborative colleagues will surround you and are always willing to lend a helping hand. The company also values continuous learning and development, providing ample opportunities for training, workshops, and skill-building activities.
Duties/Responsibilities
Under general supervision, responsible for providing support in a clinical research environment.
Performs all clinical research duties within regulatory compliance and industry guidelines as described in the Food and Drug Administration (FDA), Good Clinical Practices (GCP), International Conference on Harmonization (ICH), Health Insurance Portability and Accountability Act (HIPPA), institutional review boards (IRB), TVCR policies and standard operating procedures (SOP), and sponsor requirements.
Answers phones according to our office policies and procedures.
Understand the importance of maintaining research subject confidentially throughout the duration and upon completion of a trial.
Perform document scanning, printing, filing, and shredding at the direction of research coordinators.
Communicate effectively with all office staff.
Scheduling patient visits.
Requesting medical records.
Receive and disperse shipments.
Basic understanding of TVCR research studies and where to locate specifics within protocols.
Prepare materials before patient visits.
Maintain inventory of clinic supplies.
Light office cleaning duties.
Perform new duties that arise due to changing clinic needs.
Work Environment and Physical Demands
The work environment and physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully.
Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
Work is performed in an office/laboratory and a clinical environment.
Exposure to biological fluids and bloodborne pathogens.
Personal protective equipment may be required, such as eyewear, garments, and gloves.
Ability to work upright and stationary for 4-6 hours daily.
Frequent mobility is required to include occasional squatting, kneeling, or bending.
Light to moderate lifting and carrying (or otherwise moving) objects, including medical equipment, with a maximum lift of 20-50 lbs.
This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee. Duties, obligations, and activities may change, or new ones may be assigned at any time, with or without notice, as the clinic needs to change and grow.
Job Type: Full-time
Pay: $10.00 - $18.00 per hour
Expected hours: 32 – 40 per week
Benefits:
401(k)
Health insurance
Paid time off
Physical Setting:
Office
Schedule:
8 hour shift
Day shift
Application Question(s):
Do you have a reliable means to and from work daily?
Language:
English and Spanish (Required)
Work Location: In person
