Job Title: Research Assistant
Scheduled Weekly Hours: 24 Hours
Job Profile Summary: This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials. The primary skills include logical thinking, the ability to prioritize, the ability to adapt quickly to changing business conditions, and strong interpersonal and team-building skills.

QUALIFICATIONS:

• Equivalent education and experience - High School Diploma and 1 years’ relevant work experience in clinical research.
• At least 1 year experience working in a clinical research setting preferred.
• Possess a working knowledge of clinical trials and the principles of Good Clinical Practices (GCP).
• In-depth knowledge of protocol and study-specific operating procedures, consent forms, and study schedules.
• Skill in carrying out required clinical procedures.
• Working knowledge of medical terminology.
• Ability to pay close attention to detail.
• Ability to establish and maintain effective working relationships with coworkers, managers, patients, physicians, and clients.
• Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies.
  Please note, this position is not eligible for sponsorship.
  

  LI-CES and #LI-DNP #LI-HCP #ONSITE

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
IQVIA’s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
The potential base pay range for this role is $25.00-$39.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits

• EDC Entry and Query Resolution
• Assist with the screening, recruiting, and enrollment of research subjects.
• Develop strong working relationships and maintain effective communication with study team members, investigators, and office staff to build a foundation of trust and respect between the clinic and the research office.
• Perform patient/research participant scheduling and collect their history.
• Coordinate follow-up care and laboratory procedures.
• Adhere to an IRB-approved protocol.
• Assist in the informed consent process of research subjects.
• Support the safety of research subjects.
• Coordinate protocol-related research procedures, study visits, and follow-up care.
• Comply with company and Sponsor policies, standard operating procedures (SOPs), and guidelines.
• Schedule subject visits and procedures.