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 at https://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.

Qualifications

Equivalent education and experience - High School Diploma and 1 years’ relevant work experience in clinical research
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

Benefits

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

Responsibilities

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
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

Site Research Assistant - Hammond, LA

Job Type