Safety Operations Intern-DL at IQVIA

Dalian, Liaoning, China

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Not SpecifiedCompensation

InternshipExperience Level

InternshipJob Type

UnknownVisa

Life Sciences, Healthcare, Pharmaceuticals, Clinical ResearchIndustries

Requirements

Passed Japanese N2 certification or equivalent Japanese proficiency level
Passed university English CET4 or above
Bachelor's degree or above; Japanese major acceptable; biology or pharmaceutical background preferred
Able to commit to at least 24-32 hours per week
Location: Dalian office (Dalian High-tech Park, Tengfei Software Park Phase I, West Wing, 10th Floor); accepts combination of remote and on-site internship

Responsibilities

Assist supervisor in handling drug adverse reaction safety data, including: collecting and tracking incoming adverse events (AE)/endpoint information, determining initial/update status of incoming events, tracking event processing timelines, etc
Assist supervisor in managing project workflows, including database entry, quality control activities, generation of drug safety data reports, preparation of drug safety submission dossiers, etc
Other assisting tasks assigned by the supervisor

Skills

Key technologies and capabilities for this role

Japanese N2English CET4Adverse Event TrackingDatabase EntryQuality ControlSafety Data ManagementPharmacovigilanceReport Generation

Questions & Answers

Common questions about this position

What is the work arrangement for this internship?

The position is part-time, requiring at least 24-32 hours per week, and accepts a combination of remote and on-site work at the Dalian office.

What language and education requirements are needed for this role?

Candidates must have passed Japanese N2 or equivalent proficiency, university English CET4 or above, and a bachelor's degree or higher; Japanese majors or those with biology/pharmaceutical backgrounds are preferred.

Is there a chance for full-time employment after the internship?

Successfully passing the internship assessment allows priority consideration for a full-time offer.

Where is the internship located?

The internship is based at the Dalian office in Tengfei Software Park Phase I West Wing, 10th Floor, High-tech Zone, Dalian City, with remote and on-site options.

What makes a strong candidate for this Safety Operations Intern position?

Strong candidates will have a bachelor's degree, Japanese N2 proficiency, CET4 English, and preferably a background in biology or pharmaceuticals, while committing to 24-32 hours weekly.

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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