Clinical Research Coordinator - West Seneca, NY at IQVIA

West Seneca, New York, United States

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Part TimeJob Type

UnknownVisa

Healthcare, Clinical ResearchIndustries

Requirements

High School Diploma and 1 years’ relevant work experience in clinical research (equivalent education and experience accepted)
At least 1 year experience working in a clinical research setting preferred
Applicable certifications and licenses as required by company, country, state, and/or other regulatory bodies
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 (phlebotomy required; pediatric experience needed)
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

Responsibilities

Perform a variety of complex clinical procedures on subjects including but not limited to ECG, sample collection including spirometry, vital signs, and phlebotomy
Coordinate clinical research studies conducted by a supervising principal investigator
Update and maintain skills, training, and knowledge of current best nursing practices and topics related to clinical research
Safeguard the well-being of subjects and maintain high standards, including maintaining a safe environment in accordance with Health and Safety policies
Act as a volunteer advocate and address volunteer and visitor concerns proactively
Assist staff in clinical coordinator practices and delivery of care to volunteers; report deviations from normal practice to senior staff
Review study protocol, case report form (CRF), other study documents, and electronic data capture systems
Participate in project meetings, huddles, and troubleshooting study issues
Perform clinical set-up and preparation for studies (e.g., labeling specimen tubes, setting up equipment, planning logistics, generating volunteer instructions, obtaining supplies)
Prepare and deliver study-specific training materials, documents, and records
Recruit and screen volunteers based on pre-determined criteria; orient volunteers to the study and site
Assist with data quality checking, query resolution, and ensuring quality control for accuracy and completeness
Responsible for correct administration and custody of study drug according to site standard operating procedures
Collect, record, and report clinical data and findings in CRFs; collaborate with study investigator on adverse events
Cooperate with study monitor and follow ICH GCP guidelines for all study and patient activities
Participate in community outreach

Skills

Phlebotomy

ECG

Spirometry

Vital Signs

Sample Collection

Pediatric Experience

Clinical Research Coordination

Study Protocol Review

Electronic Data Capture

Data Quality Checking

Query Resolution

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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