Experienced Clinical Research Associate at IQVIA

Reading, England, United Kingdom

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

NoVisa

Life Sciences, Healthcare, Clinical ResearchIndustries

Requirements

Experience of independent on-site monitoring in the UK
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility to travel to sites as required

Responsibilities

Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits) in partnership with a single-sponsor
Working with sites to adapt, drive and track subject recruitment plan
Providing protocol and study training to assigned sites
Creating and maintain monitoring visit reports and action plans
If appropriate, co-monitoring, training and mentoring junior members of the team

Skills

Key technologies and capabilities for this role

GCPICHSite MonitoringSite ManagementSite InitiationRoutine MonitoringClose-out VisitsSubject RecruitmentProtocol TrainingMonitoring Reports

Questions & Answers

Common questions about this position

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

This information is not specified in the job description.

Is this a remote position or does it require travel?

The role requires flexibility to travel to sites as required and includes independent on-site monitoring in the UK.

What are the key requirements for this Clinical Research Associate role?

Candidates need experience of independent on-site monitoring in the UK, in-depth knowledge of Good Clinical Practice (GCP) and ICH guidelines, and a life science degree or equivalent industry experience.

What does the team structure look like for this role at IQVIA?

The position involves working in partnership with a single sponsor and, if appropriate, co-monitoring, training, and mentoring junior members of the team.

What makes a strong candidate for this CRA position?

Strong candidates will have experience in independent on-site monitoring in the UK, deep GCP and ICH knowledge, a life science degree or equivalent, and the flexibility to travel; UK work eligibility is required as visa sponsorship is not offered.

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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