Sr Site Activation Coordinator at IQVIA

Dalian, Liaoning, China

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Not SpecifiedCompensation

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

Full TimeJob Type

UnknownVisa

Healthcare, Clinical Research, PharmaceuticalIndustries

Requirements

Bachelor's Degree in Life Science or related field (Required)
2 years’ experience in a healthcare environment or equivalent combination of education, training and experience
Established individual contributor who works under general supervision
Delivers objectives that significantly impact results for a job area
Tasks are not typically routine, and may require applying discretion within broad operational boundaries and procedures
Problems faced are general and may require some analysis to resolve

Responsibilities

Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary
Review documents for completeness, consistency and accuracy, under guidance of senior staff
Prepare site documents, reviewing for completeness and accuracy
Inform team members of completion of regulatory, contractual, and other documents for individual sites
Distribute completed documents to sites and internal project team members
Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information
Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents

Skills

Site Activation

Feasibility Studies

Regulatory Documents

Contract Management

Ethics Submissions

Informed Consent

Project Tracking

SOP Compliance

Document Review

Database Management

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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