Site Research Assistant – Hallandale Beach, FL
Aventura, FLFull-time
Behavioral Health Market Context
Apply Nowvia Talents By Vaia
Benefits
Health Insurance
Job Description
anging 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: 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.
#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. #J-18808-Ljbffr
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: 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.
#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. #J-18808-Ljbffr
Qualifications
- •Equivalent education and experience: a minimum of an associate’s degree
- •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
- •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
More Jobs
- BCBA: Impactful ABA Leaderat Above and Beyond Therapy
- Speech Therapist - Outpatient Floatat Advocate Aurora Health
- K-5 BCBA: Classroom Coach & Behavior Interventionat Salem School District
- Licensed Mental Health Therapist - Onsite or Onlineat Therapymatch Inc. (DBA Headway)
- Behavior Technicianat LEARN Behavioral
- Pediatric Speech-Language Pathologist- Part-timeat Connect Home Health
- Registered Behavior Technician RBTat Golden Steps ABA
- Launch in ABA Behavior Technicianat BK Healthcare Management
- ABA Behavior Technician — Flexible Hours & Paid Trainingat Alora Behavioral Health
- Registered Behavior Technician RBTat One Behavioral