Clinical Research Assistant

ELLIGO HEALTH RESEARCH INC•El Paso, TX

64d

About The Position

SUMMARY: The Research Study Assistant plays a key role in assisting with the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary function of the Research Study Assistant is to support the Clinical Research Coordinators (CRCs) and the broader study team in the successful execution of clinical trials to achieve study objectives and corporate goals. This role is responsible for a variety of tasks, including administrative duties, data management/entry, patient interaction and technical procedures such as phlebotomy, performing ECGs and vital signs. Additional focus is on specimen collection, specimen handling and transport, specimen processing, lab manual creation, reviewing lab results and inventory monitoring.

Requirements

Bilingual (English/Spanish) required
Minimum 1 year of experience in clinical research or a patient facing, clinical setting
Clear and concise written and oral communication skills to interact effectively with coworkers and study staff (including sponsor/CRO).
Strong organizational skills including the ability to accomplish multiple tasks within established timeframes through effective prioritization of duties and functions in a fast-paced environment.
Ability to recognize and synthesize information
Ability to act and operate independently with minimal daily direction from manager to accomplish objectives
Strong attention to detail and accuracy
Excellent interpersonal and customer relationship skills
Aptitude to work effectively and positively with a team and diverse group of individuals
Basic skill level with word processing, spreadsheet, database, and presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint)

Nice To Haves

Associates degree a plus
Certification in phlebotomy, ECGs or similar clinical skills preferred
Experience with Athena EMR preferred
Basic knowledge of medical terminology preferred

Responsibilities

Maintain a safe, clean working environment, including infection control requirements
Perform specimen collections, includes venipuncture to pediatric and adult participants
Process specimens received in the laboratory. This task includes specimen transport, handling, sorting, requisition entry, inventory accountability, and reviewing lab results for PI review.
Performing CLIA waived testing such as urine pregnancy testing, urine dip analysis, urine drug screen testing, alcohol testing, Rapid Antigen Testing
Ensure specimen collection/processing/shipping are performed according to protocol
Complete study training and available for additional duties to support study conduct as needed, which may include:
Assist with the screening, recruiting and enrollment of research subjects.
Assist in the informed consent process of research subjects
Collect patient/research participant history
Data entry and Management per Good Documentation Practice
Coordinate follow-¬up care and laboratory procedures
Support the collection and review of required essential study documents and reports. Order supportive study supplies (e.g., contracts, IXRS, lab kits, non-¬ clinical supply materials, imaging and laboratory handling manuals, etc.)
Performing vitals, ECG, spirometry
Coordinate protocol related research procedures, study visits, and follow-¬up care
Develop strong working relationships and maintain effective communication with study team members
Develop strong working relationships with the investigators and staff to build a foundation of trust and respect
Adhere to an IRB approved protocol
Support the safety of research subjects
Comply with Elligo, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelines
Perform other duties as required and/or assigned.