Research Assistant

Research Assistant (Medical Assistant/Phlebotomist/CNA/EMT/Paramedic) - PRN- 100% on site San Antonio TX

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Research Assistant (PRN) to join our diverse and dynamic team. The Research Assistant is integral in the execution of all aspects of the clinical trial, will have direct patient contact and is responsible for ensuring that all clinical trial activities are performed as outlined by the clinical trial protocol. As a Research Assistant, you will also be responsible for performing the task(s) as per clinical trial protocol, ICON Early Phase Services SOPs, FDA, ICH GCP, and utilizing proper source documentation techniques; and participate in clinical trial meetings and training as warranted by the study protocols.

Title: Research Assistant

Job Type: PRN

Location: 100% on site San Antonio TX

Desired Shift/Schedule: Day Shift > Weekends

What you will be doing :

• Responsible for clarifying any clinical trial related issues to ensure proper execution of clinical trial.

• Collection of Pharmacokinetic specimens.

• Apply all IEP CRU Standard Operating Procedures (SOP) applicable to job duties.

• Familiarize and understand protocol requirements.

• Participate in all internal and external clinical trial meetings, as appropriate.

• Quality checks all completed source documents to ensure accuracy, legibility and completion of all data points.

• Ensure the collection of data and dataflow through the QC process (e.g. completion of internal queries).

• Participate in the QC execution and review of study documents (e.g. source documents, informed consents).

• Collection and transport of laboratory specimens (e.g. blood and urine).

• Ensure proper use of all medical equipment and supplies.

• Proper disposal of bio-hazardous waste.

• Participate in all clinical trial meetings and trainings as warranted.

• Give report to incoming research assistants.

• Ensure compliance with all applicable regulations (e.g. OSHA, FDA, etc.).

• Follow any reasonable directive.

• To undertake other reasonably related duties as may be assigned from time to time

Your profile:

• Minimum of one-year experience in clinical research or related fields.

• High School Diploma or equivalency with medical assistant training/certification or other allied health certification

• Medical Assistant, Phlebotomy Technician, Paramedic, EMT, LVN, or RN preferably with two years of experience;

• Maintains current job-related competencies, certifications, and/or licensure.

What ICON can offer you:

Visit our careers site to read more about the benefits ICON offers.

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment.  All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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