Site Research Assistant - Miami, FL at IQVIA

Miami, Florida, United States

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Not SpecifiedCompensation

Entry Level & New GradExperience Level

Part TimeJob Type

UnknownVisa

Healthcare, Clinical ResearchIndustries

Requirements

High School Diploma and 1 year relevant work experience in clinical research (equivalent education and experience accepted)
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

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

Skills

Key technologies and capabilities for this role

EDC EntryQuery ResolutionClinical TrialsGood Clinical PracticesIRB ProtocolsInformed ConsentPatient ScreeningPatient SchedulingMedical TerminologyClinical Procedures

Questions & Answers

Common questions about this position

Is this a full-time or part-time position?

This is a part-time position with 29 scheduled weekly hours.

What is the work setup for this role?

The position requires working on-site in Miami, FL.

What skills are required for this Research Assistant position?

Key skills include logical thinking, ability to prioritize and adapt quickly, strong interpersonal and team-building skills, working knowledge of clinical trials and Good Clinical Practices (GCP), and attention to detail.

What qualifications are needed for this role?

A High School Diploma with 1 year of relevant work experience in clinical research is required, preferably at least 1 year in a clinical research setting, along with knowledge of medical terminology and applicable certifications.

What makes a strong candidate for this position?

Strong candidates will have experience in clinical research, knowledge of GCP and medical terminology, plus skills in building relationships, attention to detail, and performing clinical procedures.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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