Site Research Assistant - Atlanta, GA

IQVIA Argentina; Atlanta (GA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading global provider of clinical research services is seeking a Research Assistant in Atlanta. This role involves assisting with clinical trial activities, maintaining communication with study teams, and ensuring adherence to protocols. Ideal candidates will have strong interpersonal skills, attention to detail, and relevant experience in clinical research. Join a dynamic team dedicated to improving patient outcomes and advancing medical treatments.

Qualifications

• 1 year relevant work experience in clinical research.
• Working knowledge of clinical trials and Good Clinical Practices (GCP).

Responsibilities

• Assist in clinical trial activities and patient scheduling.
• Develop relationships with study team members and investigators.
• Adhere to IRB-approved protocols and coordinate research procedures.

Skills

Logical Thinking

Interpersonal Skills

Team-Building Skills

Attention to Detail

Education

High School Diploma

Job description

Job Title:Research Assistant

Work Set-Up:Working On-site
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.

Responsibilities:

• EDC Entry and Query Resolution
• Develop strong working relationships and maintain effective communication with study team members.
• Develop strong working relationships with the investigators and office staff to build a foundation of trust and respect between the clinic and the research office.
• Assist with the screening, recruiting, and enrollment of research subjects.
• Perform patient/research participant scheduling.
• Collect patient/research participant 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.

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.
• Working knowledge of clinical trials.
• Working knowledge of 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 athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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.