Job Description

Job Description

Job Description

SUMMARY

The Research Assistant I plays a critical role in supporting the operational and administrative aspects of clinical trials. This position is responsible for ensuring compliance with research protocols, assisting with patient enrollment, and maintaining accurate data entry while collaborating with internal teams and external partners. This is an onsite position, requiring hands-on involvement in clinical research activities.

ESSENTIAL DUTIES

• Provide operational and administrative support for the day-to-day execution of clinical trials.
• Ensure adherence to established Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) guidelines, and other applicable regulatory requirements.
• Obtain informed consent from patients for clinical research studies.
• Create and maintain patient files and charts for clinical studies.
• Accurately enter patient enrollment and medical history data into electronic data capture (EDC) systems.
• Address and resolve queries within the EDC system in a timely manner.
• Conduct vital sign measurements, nasal swabs, and blood processing as needed for proper study enrollment.
• Organize, coordinate, and process lab supplies to support clinical trial operations.
• Establish and maintain relationships with external partners and vendors.
• Evaluate study performance by gathering, analyzing, and interpreting key data and metrics.

WORK ENVIRONMENT

• Clinical office environment
• May involve some exposure to hazards or physical risks, which require following basic safety precautions
• Occasional night and weekend work schedules may be required

PHYSICAL DEMANDS

• Frequent use of keyboard and mouse
• Frequent use of computer monitors and other electronic screens
• Frequent standing, walking, bending, and stooping
• Occasional ability to lift 10 pounds
• Ability to differentiate colors according to study protocols

EDUCATION & EXPERIENCE

REQUIRED

• High School Diploma or Equivalent
• Strong attention to detail in data entry and patient record management.
• Understanding of laboratory supply coordination and management.
• Proficiency in EDC systems for tracking patient enrollment and medical history.
• Ability to perform basic clinical procedures such as vital signs, nasal swabs, and blood processing.
• Excellent organizational and multitasking skills for handling multiple research-related tasks.
• Effective communication skills for collaborating with internal teams and external partners.

PREFERRED

• MA-R and/or MA-P certification
• Background in biology, health sciences, or a related field is a plus.
• Familiarity with informed consent processes and patient engagement strategies.
• Knowledge of clinical research operations, including Good Clinical Practice guidelines.

TRAVEL

At least 5% travel within the geographic region of the assigned work location.

OTHER DUTIES

In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.

EEO STATEMENT

ERA Health Research (ERA) provides equal employment opportunities to all without regard to race, color, religion, sex (including sexual orientation or gender identity), national origin, age, disability, genetic information, or other protected status. Applicants and employees with disabilities may be entitled to reasonable accommodations under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is an adjustment to our standard application and/or interview and/or employment process which will ensure an equal employment opportunity without imposing undue hardship on ERA. Please inform our team if you are requesting accommodation to complete any forms or otherwise participate in the application process or perform the essential functions of this role.

Job Tags

Similar Jobs