Full Job Description
Clinical Research Assistant Needed
To join a rapidly growing clinical research team involved in pulmonary research with plans for further expansion into other areas.
Very competitive salary and benefits to include 401K; commensurate with experience.
Job Type: Full-time
Monday through Friday 8am to 4:30pm
Duties and Responsibilities
Day-to-day activities may include all or some of the essential functions listed below, depending upon individual experience, knowledge and the needs of the organization which are subject to change from time to time.
- Assists in recruiting participants and assessing patient eligibility for the approved study.
- The research associate is primarily responsible for assisting in research patient visits according to ICH-GCP guidelines, and according to the IRB-approved study protocol and/or manual of procedures.
- Review and comprehend all study protocols assigned, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, and privacy protections.
- Coordinate and schedule subject visits within study/subject specific windows per protocol guidelines.
- Conducts and/or participates in the informed consent process/discussion with research participants, including answering any questions related to the study.
- Obtains appropriate signatures and dates on forms in appropriate places per the research SOP.
- Assures that amended consent forms are appropriately implemented and signed respectively.
- Accurately collect and record all necessary data for follow up, screening and randomization study visits (e.g., demographics, medical history, adverse events, concomitant medications, etc.).
- Collection, processing, and shipment of laboratory biological samples for analysis
- Review and resolve data management queries as needed
- Assist/perform with treatment preparation and administration (on selected studies, as assigned)
- Assist Coordinator with maintaining IP/device accountability and shipping logs (on selected studies, as assigned)
- Serious Adverse Event Reporting initial & follow up reporting, including promptly request all necessary medical records, review of medical records and updated reporting
- Training/Understanding all aspects of regulatory
- Assist Coordinator in CTMS management (when available)
- Perform other duties as assigned
Requirements and Qualifications
- BS or AS degree in science, health administration, or experience equivalent (Preferred)
- 1-2 years of Clinical Research experience or equivalent (Required)
- Eager to learn and grow professionally
- Proficient computer skills, including Microsoft Office Suite
- Self-directed and able to work without supervision
- Excellent written and verbal communication skills
- Ability to multitask, prioritize, and manage time efficiently
- Detail oriented, honest, and reliable
Job Type: Full-time
Schedule:
- 8 hour shift
Experience:
- Research: 1-2 years (Preferred)
Work Location:
- One location
Job Type: Full-time
Pay: $15.00 – $18.50 per hour
Schedule:
- 8 hour shift
COVID-19 considerations:
All patients and staff must wear a mask.
Experience:
- Research: 2 years (Preferred)
Work Location: One location
Source: Indeed.com
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