Clinical Research Coordinator - Troy, NY at IQVIA

Troy, New York, United States

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Not SpecifiedCompensation

Junior (1 to 2 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)
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
Phlebotomy skills required
Pediatric experience required
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

Responsibilities

Perform phlebotomy and a variety of complex clinical procedures on subjects including but not limited to ECG, sample collection including spirometry, and vital signs
Conduct community outreach
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, taking remedial action as required
Assist staff in clinical coordinator practices and the delivery of care to volunteers
Report any deviation 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 with the project team as needed
Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, setting up equipment and documents
Plan logistical activity for procedures as per protocol
Generate volunteer instructions
Identify and obtain required supplies and equipment
Prepare and deliver study-specific training materials, documents, and records
Troubleshoot study issues
Participate in huddles to ensure daily tasks assigned to team members are executed to expected standards
Assist with data quality checking and query resolution to ensure data adheres to study protocol and quality control for accuracy and completeness
Recruit and screen volunteers for inclusion in the study based on pre-determined criteria
Orient volunteers to the study and site, including purpose, procedures, and practical issues such as visit timelines
Administer and maintain custody of study drug according to site standard operating procedures
Collect, record, and report clinical data and findings in case report forms (CRFs)
Collaborate with study investigator, informing on relevant adverse events and serious adverse events per protocol
Cooperate with study monitor and reserve time for questions during monitoring
Follow ICH GCP guidelines for all study and patient activities

Skills

Phlebotomy

ECG

Spirometry

Vital Signs

Clinical Research

Study Protocol Review

Sample Collection

Data Quality Checking

Query Resolution

Community Outreach

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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