Clinical Research Associate, Sponsor Dedicated at IQVIA

Durham, North Carolina, United States

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$64,000 – $189,000Compensation

Entry Level & New Grad, Junior (1 to 2 years)Experience Level

Full TimeJob Type

NoVisa

Clinical ResearchIndustries

Requirements

Bachelor’s degree in a health care or other scientific discipline, or equivalent
Successful completion of a CRA Trainee Program
Or at least three months of on-site monitoring experience
Strongly Preferred: 2 years of clinical research coordinator experience
Alternatively, an equivalent combination of education, training, and experience
Good basic knowledge of applicable clinical research regulatory requirements

Responsibilities

Performing site selection, initiation, monitoring, and close-out visits
Maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication and administering protocol training to assigned sites
Evaluating the quality and integrity of site practices, escalating quality issues as needed
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Collaborating and communicating with various colleagues and customers

Skills

Key technologies and capabilities for this role

Site SelectionMonitoring VisitsSite InitiationClose-out VisitsProtocol TrainingRegulatory SubmissionsCRF CompletionData Query ResolutionSubject RecruitmentClinical Research Regulations

Questions & Answers

Common questions about this position

What is the salary range for this Clinical Research Associate position?

The annualized base pay ranges from $64,000.00 to $189,000.00.

Is this position remote or does it require specific location requirements?

The location type is not specified, but to be eligible, you must reside in the same country where the job is located.

What are the key requirements and experience needed for this role?

A Bachelor’s degree in a health care or scientific discipline is required, along with successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience. Strongly preferred is 2 years of clinical research coordinator experience, plus good basic knowledge of clinical research regulatory requirements.

What career development opportunities does this role offer?

This role is an ideal stepping-stone for CRAs, offering training, development, dedicated mentoring, structured performance reviews, access to cutting-edge technology, and global project work.

How should I apply for this position and what makes a strong candidate?

Apply through the IQVIA careers website at https://jobs.iqvia.com, and ensure you reside in the same country as the job location. Strong candidates will have a Bachelor’s degree in a scientific field, CRA trainee completion or monitoring experience, and preferably 2 years as a clinical research coordinator.

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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