IQVIA
Site Research Assistant - Winter Park, FL
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Site Research Assistant - Winter Park, FL
role at
IQVIA
Overview This position supports the conduct of clinical trial activities in compliance with applicable regulations. Primary skills include logical thinking, prioritization, adaptability to changing conditions, and strong interpersonal and team-building abilities.
Responsibilities
EDC Entry and Query Resolution
Develop strong working relationships and maintain effective communication with study team members
Develop strong working relationships with investigators and office staff to build trust between the clinic and the research office
Assist with 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, SOPs, and guidelines
Schedule subject visits and procedures
Qualifications
Equivalent education and experience: a minimum of an associate’s degree
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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. Learn more at IQVIA jobs. 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. Learn more at IQVIA jobs/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 factors including qualifications, location, and schedule. Depending 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.
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Site Research Assistant - Winter Park, FL
role at
IQVIA
Overview This position supports the conduct of clinical trial activities in compliance with applicable regulations. Primary skills include logical thinking, prioritization, adaptability to changing conditions, and strong interpersonal and team-building abilities.
Responsibilities
EDC Entry and Query Resolution
Develop strong working relationships and maintain effective communication with study team members
Develop strong working relationships with investigators and office staff to build trust between the clinic and the research office
Assist with 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, SOPs, and guidelines
Schedule subject visits and procedures
Qualifications
Equivalent education and experience: a minimum of an associate’s degree
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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. Learn more at IQVIA jobs. 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. Learn more at IQVIA jobs/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 factors including qualifications, location, and schedule. Depending 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.
#J-18808-Ljbffr