Site Activation Manager (evergreen) at IQVIA

Taipei, Taiwan

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, Clinical ResearchIndustries

Requirements

Bachelor’s Degree in Life Sciences or a related field
7 years’ relevant experience in a scientific or clinical environment, including demonstrable experience in an international role

Responsibilities

Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects, adhering to project timelines
Develop, implement, and maintain the Management Plan according to the Scope of Work and Project Plan
Resolve project-related issues as required
Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries
Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance
Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation, and maintenance of clinical trials
Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase
Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations
Identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan
Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis, and dissemination of accurate regulatory intelligence
Execute operational strategy/expectations for maintenance of clinical study approvals, authorizations, and review/negotiation of contracts and essential documents
Work with Quality Management to ensure appropriate quality standards
Mentor and coach colleagues as required
Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines, and project plans
May take a lead role in developing long-standing relationships with preferred IQVIA customers
Deliver presentations/training to clients, colleagues, and professional bodies as required
May be involved in activities related to monthly study budget planning and reviews

Skills

Key technologies and capabilities for this role

Site ActivationRegulatory AffairsClinical Trial ManagementProject ManagementBudget ManagementResource ManagementRegulatory StrategyBusiness DevelopmentBid DefenseRegulatory Intelligence

Questions & Answers

Common questions about this position

What is the salary range for the Site Activation Manager position?

This information is not specified in the job description.

Is this a remote position or is there a required location?

This information is not specified in the job description.

What education and experience are required for this role?

A Bachelor’s Degree in Life Sciences or a related field is required, along with 7 years’ relevant experience in a scientific or clinical environment, including demonstrable experience in an international role.

What does the team structure or company culture look like?

This information is not specified in the job description.

What makes a strong candidate for the Site Activation Manager role?

Strong candidates will have a Bachelor’s Degree in Life Sciences or related field, 7 years of relevant experience in scientific or clinical environments with international exposure, and skills in managing site activation, regulatory strategies, and multi-protocol programs.

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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